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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2006-05-22 14:17:34 UTC

Update Date

2021-09-14 15:19:28 UTC

HMDB ID

HMDB0002065

Secondary Accession Numbers

HMDB02065

Metabolite Identification

Common Name

6-Lactoyltetrahydropterin

Description

6-Lactoyltetrahydropterin is a putative intermediate in the de novo synthesis of tetrahydrobiopterin (BH4) pathway, in a reaction involving the enzyme sepiapterin reductase (E.C. 1.1.1.153) in human liver. In brain, an enzyme distinct from sepiapterin reductase catalyzes the TPNH-dependent reduction of 6-pyruvoyl-tetrahydropterin to 6-lactoyl-tetrahydropterin. (PMID: 4004850 ). In brain, the expression of other enzymes involved in BH4 biosynthesis includes aldose reductase, carbonyl reductase, GTP-cyclohydrolase I, and 6-pyruvoyltetrahydrobiopterin. Sepiapterin reductase expression is increased in Parkinson's disease brain tissue. (PMID: 17270157 ).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0002065
     RDKit          3D
6-Lactoyltetrahydropterin
 30 31  0  0  0  0  0  0  0  0999 V2000
   -4.0437    0.2950   -0.5230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4142    0.1874    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9355    1.1699    1.6582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9579    0.1877    0.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4077    1.0038    1.6416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0287   -0.7041    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8267   -0.0911   -1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3673    0.7287   -1.2682 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6003    0.2813   -0.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131    0.5754   -1.2222 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9484    0.1228   -0.6699 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2226    0.4360   -1.1728 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8532   -0.6602    0.4159 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6700   -0.9983    0.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -1.7315    1.9743 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5060   -0.5318    0.3874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2251   -0.8052    0.8578 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8362    1.2769   -0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7848   -0.4884   -1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2803   -0.3437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7563   -0.7981    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4047    1.8360    1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.7354    0.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057   -0.9864   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850    0.4909   -1.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3750    1.7080   -1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6207   -0.0240   -2.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7936    1.1540   -0.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7031   -1.0537    0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1346   -1.1257    1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17  6  1  0
 16  9  2  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 13 29  1  0
 17 30  1  0
M  END

 
  Mrv0541 02231219202D          
 
 17 18  0  0  0  0            999 V2000
    9.9210  -11.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9210  -10.1742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6452  -11.4226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2007  -11.4226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.6414   -9.7518    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2007   -9.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3919  -11.0680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4916  -11.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3655  -10.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4916  -10.1742    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2007   -8.9446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7788  -11.4113    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.0746   -9.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7836  -10.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0784   -8.9371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4965   -9.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7836  -10.9851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  1  4  1  0  0  0  0
  2  5  1  0  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  4  8  2  0  0  0  0
  5  9  1  0  0  0  0
  6 10  1  0  0  0  0
  6 11  2  0  0  0  0
  8 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0002065

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(O)C(=O)C1CNC2=C(N1)C(=O)NC(N)=N2

> <INCHI_IDENTIFIER>
InChI=1S/C9H13N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3-4,12,15H,2H2,1H3,(H4,10,11,13,14,17)

> <INCHI_KEY>
HKCYZTKHPLJZDR-UHFFFAOYSA-N

> <FORMULA>
C9H13N5O3

> <MOLECULAR_WEIGHT>
239.2312

> <EXACT_MASS>
239.101839307

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
22.58968228071039

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-6-(2-hydroxypropanoyl)-3,4,5,6,7,8-hexahydropteridin-4-one

> <ALOGPS_LOGP>
-1.55

> <JCHEM_LOGP>
-1.7059502636666668

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.6656059189372

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.117783698142386

> <JCHEM_PKA_STRONGEST_BASIC>
4.6153386692917575

> <JCHEM_POLAR_SURFACE_AREA>
128.84

> <JCHEM_REFRACTIVITY>
67.8667

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.21e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-lactoyl tetrahydropterin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0002065
     RDKit          3D
6-Lactoyltetrahydropterin
 30 31  0  0  0  0  0  0  0  0999 V2000
   -4.0437    0.2950   -0.5230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4142    0.1874    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9355    1.1699    1.6582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9579    0.1877    0.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4077    1.0038    1.6416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0287   -0.7041    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8267   -0.0911   -1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3673    0.7287   -1.2682 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6003    0.2813   -0.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131    0.5754   -1.2222 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9484    0.1228   -0.6699 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2226    0.4360   -1.1728 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8532   -0.6602    0.4159 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6700   -0.9983    0.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -1.7315    1.9743 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5060   -0.5318    0.3874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2251   -0.8052    0.8578 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8362    1.2769   -0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7848   -0.4884   -1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2803   -0.3437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7563   -0.7981    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4047    1.8360    1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.7354    0.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057   -0.9864   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850    0.4909   -1.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3750    1.7080   -1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6207   -0.0240   -2.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7936    1.1540   -0.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7031   -1.0537    0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1346   -1.1257    1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17  6  1  0
 16  9  2  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 13 29  1  0
 17 30  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      18.519 -20.541   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.519 -18.992   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      19.871 -21.322   0.000  0.00  0.00           N+0
HETATM    4  N   UNK     0      17.175 -21.322   0.000  0.00  0.00           N+0
HETATM    5  N   UNK     0      19.864 -18.203   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      17.175 -18.224   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.265 -20.660   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.851 -20.541   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.216 -18.978   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      15.851 -18.992   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0      17.175 -16.697   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0      14.520 -21.301   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      22.539 -18.210   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      23.863 -18.978   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      22.546 -16.683   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      25.193 -18.210   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      23.863 -20.506   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7                                                       
CONECT    4    1    8                                                       
CONECT    5    2    9                                                       
CONECT    6    2   10   11                                                  
CONECT    7    3    9                                                       
CONECT    8    4   12   10                                                  
CONECT    9    5   13    7                                                  
CONECT   10    6    8                                                       
CONECT   11    6                                                            
CONECT   12    8                                                            
CONECT   13    9   14   15                                                  
CONECT   14   13   16   17                                                  
CONECT   15   13                                                            
CONECT   16   14                                                            
CONECT   17   14                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

COMPND    HMDB0257759
HETATM    1  C1  UNL     1      -3.414  -0.240   1.046  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.482   0.263  -0.322  1.00  0.00           C  
HETATM    3  O1  UNL     1      -4.438  -0.497  -1.058  1.00  0.00           O  
HETATM    4  C3  UNL     1      -2.250   0.236  -1.131  1.00  0.00           C  
HETATM    5  O2  UNL     1      -2.454  -0.024  -2.314  1.00  0.00           O  
HETATM    6  C4  UNL     1      -0.866   0.463  -0.774  1.00  0.00           C  
HETATM    7  C5  UNL     1      -0.121  -0.232  -2.004  1.00  0.00           C  
HETATM    8  N1  UNL     1       1.284  -0.109  -1.877  1.00  0.00           N  
HETATM    9  C6  UNL     1       1.951  -0.077  -0.627  1.00  0.00           C  
HETATM   10  N2  UNL     1       3.273   0.052  -0.479  1.00  0.00           N  
HETATM   11  C7  UNL     1       3.811   0.070   0.791  1.00  0.00           C  
HETATM   12  N3  UNL     1       5.219   0.233   0.852  1.00  0.00           N  
HETATM   13  N4  UNL     1       3.008  -0.041   1.887  1.00  0.00           N  
HETATM   14  C8  UNL     1       1.702  -0.167   1.735  1.00  0.00           C  
HETATM   15  O3  UNL     1       0.941  -0.262   2.730  1.00  0.00           O  
HETATM   16  C9  UNL     1       1.097  -0.193   0.475  1.00  0.00           C  
HETATM   17  N5  UNL     1      -0.308  -0.336   0.285  1.00  0.00           N  
HETATM   18  H1  UNL     1      -4.425  -0.153   1.498  1.00  0.00           H  
HETATM   19  H2  UNL     1      -3.174  -1.321   1.114  1.00  0.00           H  
HETATM   20  H3  UNL     1      -2.755   0.368   1.706  1.00  0.00           H  
HETATM   21  H4  UNL     1      -3.919   1.275  -0.325  1.00  0.00           H  
HETATM   22  H5  UNL     1      -5.135  -0.785  -0.450  1.00  0.00           H  
HETATM   23  H6  UNL     1      -0.556   1.460  -0.772  1.00  0.00           H  
HETATM   24  H7  UNL     1      -0.548   0.180  -2.905  1.00  0.00           H  
HETATM   25  H8  UNL     1      -0.435  -1.327  -1.879  1.00  0.00           H  
HETATM   26  H9  UNL     1       1.920  -0.051  -2.720  1.00  0.00           H  
HETATM   27  H10 UNL     1       5.786  -0.590   1.058  1.00  0.00           H  
HETATM   28  H11 UNL     1       5.590   1.179   0.710  1.00  0.00           H  
HETATM   29  H12 UNL     1       3.483  -0.005   2.825  1.00  0.00           H  
HETATM   30  H13 UNL     1      -0.786  -0.973   0.925  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    4   21
CONECT    3   22
CONECT    4    5    5    6
CONECT    6    7   17   23
CONECT    7    8   24   25
CONECT    8    9   26
CONECT    9   10   16   16
CONECT   10   11   11
CONECT   11   12   13
CONECT   12   27   28
CONECT   13   14   29
CONECT   14   15   15   16
CONECT   16   17
CONECT   17   30
END

HMDB0002065
     RDKit          3D
6-Lactoyltetrahydropterin
 30 31  0  0  0  0  0  0  0  0999 V2000
   -4.0437    0.2950   -0.5230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4142    0.1874    0.8193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9355    1.1699    1.6582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9579    0.1877    0.8866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4077    1.0038    1.6416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0287   -0.7041    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8267   -0.0911   -1.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3673    0.7287   -1.2682 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6003    0.2813   -0.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131    0.5754   -1.2222 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9484    0.1228   -0.6699 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2226    0.4360   -1.1728 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8532   -0.6602    0.4159 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6700   -0.9983    0.9571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -1.7315    1.9743 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5060   -0.5318    0.3874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2251   -0.8052    0.8578 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8362    1.2769   -0.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7848   -0.4884   -1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    0.2803   -0.3437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7563   -0.7981    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4047    1.8360    1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424   -1.7354    0.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7057   -0.9864   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6850    0.4909   -1.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3750    1.7080   -1.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6207   -0.0240   -2.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7936    1.1540   -0.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7031   -1.0537    0.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1346   -1.1257    1.8550 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17  6  1  0
 16  9  2  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
 12 27  1  0
 12 28  1  0
 13 29  1  0
 17 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Amino-6-lactoyl-5,6,7,8-tetrahydropteridin-4(3H)-one	ChEBI
6-1'-oxo-2'-Hydroxypropyl tetrahydropterin	ChEBI
6-Lactoyl tetrahydropterin	HMDB
6-Lactoyl-5,6,7,8-tetrahydropterin	HMDB
Lactoyl-H4-pterin	HMDB
Lactoyl-PH4	HMDB
1'-oxo-2'-Hydroxypropyl-tetrahydropterin	MeSH, HMDB

Chemical Formula

C₉H₁₃N₅O₃

Average Molecular Weight

239.2312

Monoisotopic Molecular Weight

239.101839307

IUPAC Name

2-amino-6-(2-hydroxypropanoyl)-3,4,5,6,7,8-hexahydropteridin-4-one

Traditional Name

6-lactoyl tetrahydropterin

CAS Registry Number

33405-80-0

SMILES

CC(O)C(=O)C1CNC2=C(N1)C(=O)NC(N)=N2

InChI Identifier

InChI=1S/C9H13N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3-4,12,15H,2H2,1H3,(H4,10,11,13,14,17)

InChI Key

HKCYZTKHPLJZDR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterins and derivatives. These are polycyclic aromatic compounds containing a pterin moiety, which consist of a pteridine ring bearing a ketone and an amine group to form 2-aminopteridin-4(3H)-one.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Pterins and derivatives

Direct Parent

Pterins and derivatives

Alternative Parents

Substituents

Pterin
Aminopyrimidine
Pyrimidone
Secondary aliphatic/aromatic amine
Acyloin
Pyrimidine
Alpha-aminoketone
Heteroaromatic compound
Vinylogous amide
Alpha-hydroxy ketone
1,3-aminoalcohol
Secondary alcohol
Ketone
Azacycle
Secondary amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Primary amine
Carbonyl group
Organic nitrogen compound
Amine
Alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tetrahydropterin (CHEBI:17248 )
a small molecule (6-LACTOYL-5678-TETRAHYDROPTERIN )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.21 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-1.7	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	11.12	ChemAxon
pKa (Strongest Basic)	4.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	128.84 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	67.87 m³·mol⁻¹	ChemAxon
Polarizability	22.59 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	156.381	31661259
DarkChem	[M-H]-	154.532	31661259
DeepCCS	[M+H]+	155.827	30932474
DeepCCS	[M-H]-	153.469	30932474
DeepCCS	[M-2H]-	186.355	30932474
DeepCCS	[M+Na]+	161.921	30932474
AllCCS	[M+H]+	154.1	32859911
AllCCS	[M+H-H2O]+	150.3	32859911
AllCCS	[M+NH4]+	157.6	32859911
AllCCS	[M+Na]+	158.6	32859911
AllCCS	[M-H]-	153.5	32859911
AllCCS	[M+Na-2H]-	153.5	32859911
AllCCS	[M+HCOO]-	153.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
6-Lactoyltetrahydropterin	CC(O)C(=O)C1CNC2=C(N1)C(=O)NC(N)=N2	3843.3	Standard polar	33892256
6-Lactoyltetrahydropterin	CC(O)C(=O)C1CNC2=C(N1)C(=O)NC(N)=N2	2400.5	Standard non polar	33892256
6-Lactoyltetrahydropterin	CC(O)C(=O)C1CNC2=C(N1)C(=O)NC(N)=N2	2754.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
6-Lactoyltetrahydropterin,1TMS,isomer #1	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2614.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #2	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2682.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #3	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2678.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #4	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2694.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #5	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2512.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #6	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2452.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TMS,isomer #7	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2629.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2661.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2517.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	4407.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2512.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2489.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3891.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2669.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2496.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	5138.4	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #12	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2545.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #12	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2493.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #12	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4230.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #13	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2645.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #13	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2460.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #13	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4396.4	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #14	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2525.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #14	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2469.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #14	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3857.7	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2526.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2616.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4843.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2603.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2572.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	5091.3	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2622.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2574.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4890.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2480.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2509.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	4021.4	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2546.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2582.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4212.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2654.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2437.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	4411.4	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2336.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2523.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3668.8	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2480.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2478.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3899.0	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #3	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2564.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #3	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2499.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #3	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	5077.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #4	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2451.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #4	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2501.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #4	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4179.5	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #5	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2588.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #5	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2447.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #5	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4327.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #6	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2419.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #6	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2455.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #6	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3759.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #7	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2649.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #7	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2570.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #7	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	5158.5	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #8	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2551.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #8	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2552.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #8	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4269.3	Standard polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #9	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2655.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #9	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2531.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TMS,isomer #9	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4407.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2590.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2634.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4869.7	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #10	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2530.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #10	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2603.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #10	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4765.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #11	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2536.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #11	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2580.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #11	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4539.0	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #12	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2438.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #12	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2489.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #12	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3668.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #13	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2516.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #13	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2594.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #13	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	3997.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #14	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2329.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #14	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2534.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #14	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3470.9	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2499.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2497.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3659.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #16	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2559.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #16	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2678.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #16	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4696.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #17	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2619.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #17	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2701.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #17	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4817.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #18	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2666.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #18	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2651.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #18	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4605.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2515.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2551.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3901.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2518.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2604.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4063.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2599.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2634.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4083.9	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2374.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2542.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3577.0	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2517.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2566.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3765.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2574.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2621.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4637.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2649.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2626.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4799.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2683.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2587.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4567.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2577.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2510.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3811.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #27	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2586.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #27	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2580.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #27	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4033.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #28	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2422.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #28	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2541.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #28	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3552.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2601.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2532.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3751.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2641.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2581.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4156.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2493.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2726.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4570.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2557.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2722.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4344.0	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2413.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2564.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3530.9	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2620.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2688.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4549.9	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2480.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2621.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3638.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2532.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2559.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3682.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2460.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2568.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3607.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2475.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2506.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3649.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2562.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2542.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4893.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2498.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2554.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	3998.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2649.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2503.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	4103.7	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2493.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2482.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3594.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2459.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2618.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4592.3	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2553.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2695.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4523.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2629.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2592.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4357.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2552.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2532.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3536.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2614.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2587.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	3859.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2444.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2554.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3379.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2598.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2547.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3551.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2518.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2725.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4380.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2557.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2700.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4131.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2450.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2567.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3263.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2588.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2692.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4263.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #19	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2515.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #19	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2624.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #19	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3342.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2614.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2737.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4617.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #20	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2546.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #20	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2571.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #20	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3380.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #21	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2498.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #21	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2595.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #21	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3458.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2563.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2789.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4455.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #23	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2616.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #23	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2722.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #23	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4237.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #24	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2480.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #24	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2594.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #24	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3443.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #25	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2690.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #25	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2766.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #25	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4328.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #26	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2534.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #26	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2675.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #26	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3491.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #27	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2580.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #27	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2628.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #27	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3555.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #28	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2494.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #28	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2614.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #28	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3543.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2579.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2749.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #29	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4390.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2655.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2667.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4399.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #30	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2639.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #30	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2677.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #30	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4157.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #31	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2535.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #31	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2585.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #31	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3389.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #32	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2712.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #32	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2726.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #32	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4270.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #33	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2595.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #33	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2674.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #33	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3450.3	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #34	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2660.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #34	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2604.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #34	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3507.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #35	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2566.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #35	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2614.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #35	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3535.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2589.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2815.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4086.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2449.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2713.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3226.1	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2522.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2650.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3284.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2592.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2697.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3352.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2514.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2560.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3613.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2606.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	2641.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N)=N2	3951.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2418.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	2544.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C	3429.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2545.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2579.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3600.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2550.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	2635.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C)=N2	4485.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2628.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2659.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4600.5	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2645.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2787.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4312.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2588.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2597.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #10	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3175.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2714.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2724.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #11	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4088.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2647.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2669.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #12	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3226.0	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2671.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2611.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #13	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3269.2	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2616.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2621.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #14	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3400.5	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2635.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2808.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #15	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3888.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2537.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2720.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #16	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3019.8	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2592.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2657.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #17	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3073.5	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2657.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2722.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #18	CC(O[Si](C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3122.6	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2667.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2826.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #19	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3981.9	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2657.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2723.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	4060.2	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2532.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2739.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #20	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3135.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2591.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2686.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #21	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3212.6	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2644.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2780.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #22	CC(O)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3247.8	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2682.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2814.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #23	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3901.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2553.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2746.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #24	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3131.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2662.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2667.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #25	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3189.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2714.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2771.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #26	CC(O)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3230.7	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2605.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2802.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3060.2	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2536.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2616.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3229.0	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2716.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2766.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4160.0	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2596.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2691.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #5	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3272.8	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2627.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2653.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #6	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3324.5	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2562.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	2631.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #7	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N)=N2)N1[Si](C)(C)C	3445.8	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2631.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2748.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2	4257.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2673.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	2675.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TMS,isomer #9	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2	3979.8	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2749.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2839.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3825.8	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2673.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2849.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #10	CC(O)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2962.8	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2725.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2836.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #11	CC(O)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2972.5	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2613.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2756.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #2	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2942.6	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2667.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2715.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #3	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3029.7	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2729.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2800.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #4	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3058.9	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2752.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	2809.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #5	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2	3734.7	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2646.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2737.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #6	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2939.7	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2728.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	2676.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #7	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N[Si](C)(C)C)=N2)N1[Si](C)(C)C	3007.1	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2770.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2751.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #8	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	3032.6	Standard polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2699.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2823.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,6TMS,isomer #9	CC(O[Si](C)(C)C)C(=O)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2855.5	Standard polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2767.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2875.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #1	CC(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2829.5	Standard polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2817.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2832.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,7TMS,isomer #2	CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N2)N1[Si](C)(C)C	2821.1	Standard polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2854.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #2	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2933.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #3	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2935.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #4	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	2881.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #5	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2766.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #6	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2755.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,1TBDMS,isomer #7	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	2863.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	3119.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2932.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N)=N2	4349.5	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #10	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2943.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #10	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2904.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #10	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3839.3	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #11	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3101.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #11	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	2948.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #11	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	5063.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #12	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2969.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #12	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2935.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #12	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4235.0	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #13	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3126.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #13	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	2897.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #13	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4266.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #14	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2996.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #14	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2904.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #14	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3879.1	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	2944.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3054.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #15	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4875.3	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	2999.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3019.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #16	CC(O)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	5014.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3087.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3010.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #17	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4700.1	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	2920.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	2955.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #18	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	4033.0	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3028.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3004.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #19	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4165.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	3108.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	2863.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N)=N2	4302.6	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2834.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2948.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #20	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3745.2	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	2964.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	2947.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #21	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3856.7	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	2991.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	2944.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	5029.9	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2905.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2945.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4192.7	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3057.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	2886.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4220.1	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2917.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2914.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3784.8	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #7	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3087.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #7	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3005.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #7	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	5075.0	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #8	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2976.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #8	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	2965.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #8	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4257.9	Standard polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #9	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3132.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #9	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	2935.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,2TBDMS,isomer #9	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4288.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3238.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3196.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4912.5	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3135.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3202.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4766.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3216.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3194.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4487.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3076.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3179.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3800.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3191.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3187.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4008.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	2972.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3196.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3602.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3169.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3185.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3707.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #16	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3190.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #16	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3260.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #16	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4754.7	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #17	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3230.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #17	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3266.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #17	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4795.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #18	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3323.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #18	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3207.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #18	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4546.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3150.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3179.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3884.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	3140.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	3149.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4090.0	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3259.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3181.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4090.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3023.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3142.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3663.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3218.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3190.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3763.7	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3189.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3239.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4714.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3258.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3238.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4765.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3331.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3199.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4501.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3222.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3170.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3900.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #27	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3270.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #27	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3178.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #27	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4058.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #28	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3076.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #28	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3174.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #28	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3690.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3267.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3188.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3795.0	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3306.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3122.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4144.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3114.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3321.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #30	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4610.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3240.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3313.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #31	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4337.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3035.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3224.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #32	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3691.1	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3236.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3280.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #33	CC(O)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4420.3	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3093.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3276.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #34	CC(O)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3703.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3175.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3241.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #35	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3727.4	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3142.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3230.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3699.9	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3103.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3119.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3683.8	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3231.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3139.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4880.7	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	3135.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	3122.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N)=N2	4025.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3309.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3084.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4067.2	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3126.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3111.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3674.6	Standard polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3089.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3229.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,3TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4698.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3364.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3377.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4631.1	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3466.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3329.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4332.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3334.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3338.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3733.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3472.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3315.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3943.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3227.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3328.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3601.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3424.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3338.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3702.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3263.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3464.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4465.1	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3381.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3450.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4174.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3193.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3427.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3559.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3377.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3448.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4238.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #19	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3264.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #19	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3470.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #19	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3561.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3407.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3399.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4678.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #20	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3333.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #20	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3421.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #20	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3584.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #21	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3322.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #21	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3437.8	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #21	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3655.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3352.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3481.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4503.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #23	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3462.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #23	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3402.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #23	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4238.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #24	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3281.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #24	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3393.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #24	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3626.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #25	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3482.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #25	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3431.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #25	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4293.0	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #26	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3313.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #26	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3481.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #26	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3618.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #27	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3413.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #27	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3410.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #27	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3652.3	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #28	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3397.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #28	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3416.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #28	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3711.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3371.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3478.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #29	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4459.9	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3482.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3334.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4405.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #30	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3470.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #30	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3437.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #30	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4183.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #31	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3314.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #31	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3428.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #31	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3641.7	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #32	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3487.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #32	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3469.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #32	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4239.3	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #33	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3372.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #33	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3479.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #33	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3638.6	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #34	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3445.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #34	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3410.0	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #34	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3667.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #35	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3429.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #35	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3442.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #35	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3732.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3411.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3563.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #36	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4097.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3249.9	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3547.6	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #37	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3492.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3318.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3484.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #38	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3525.8	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3375.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3532.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #39	CC(O)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3545.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3308.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3351.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3741.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3455.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	3306.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2	4015.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3212.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3309.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N)=N2)N1[Si](C)(C)C(C)(C)C	3611.2	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3401.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3362.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3714.4	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3350.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	3379.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2	4576.5	Standard polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3397.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3384.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,4TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4623.7	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3526.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3583.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #1	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4406.5	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3446.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3560.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #10	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3580.8	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3634.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3574.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #11	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4122.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3501.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3604.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #12	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3557.0	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3574.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3531.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #13	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3603.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3600.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3586.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #14	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3700.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3565.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3696.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #15	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3994.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3420.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3713.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #16	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3386.2	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3484.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3652.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #17	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3448.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3534.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3684.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #18	CC(O[Si](C)(C)C(C)(C)C)C(=O)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3450.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3633.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3632.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #19	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4058.6	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3630.5	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3514.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #2	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4148.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3470.1	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3704.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #20	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3440.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3588.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3619.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #21	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3516.2	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3611.2	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3701.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #22	CC(O)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3520.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3648.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3703.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #23	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4009.9	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3496.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3727.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #24	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3476.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3589.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3653.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #25	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3538.3	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3623.8	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3704.2	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #26	CC(O)=C(O[Si](C)(C)C(C)(C)C)C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3542.7	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3557.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3784.7	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #27	CC(O)C(=O)C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3395.6	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3447.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3544.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #3	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)[NH]C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3580.1	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3657.0	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3536.9	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #4	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4202.9	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3491.7	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3622.5	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #5	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3557.4	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3577.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3551.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #6	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CNC2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2)N1[Si](C)(C)C(C)(C)C	3608.9	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3592.6	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3572.4	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #7	CC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N([Si](C)(C)C(C)(C)C)C(N)=N2)N1[Si](C)(C)C(C)(C)C	3704.7	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3516.4	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	3617.1	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #8	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N2	4343.7	Standard polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3628.3	Semi standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	3552.3	Standard non polar	33892256
6-Lactoyltetrahydropterin,5TBDMS,isomer #9	CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=N2	4075.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (Non-derivatized) - 70eV, Positive	splash10-014i-2900000000-49dec0d6931d1e9bad0a	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (1 TMS) - 70eV, Positive	splash10-014i-2900000000-8f1d69e548d027d65a19	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 6-Lactoyltetrahydropterin GC-MS (TBDMS_1_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 10V, Positive-QTOF	splash10-006x-0090000000-a0f9d3c66da5b6d5f581	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 20V, Positive-QTOF	splash10-014i-0940000000-176c06edb35b9da14cbc	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 40V, Positive-QTOF	splash10-0kmi-4910000000-a4fc7ca72b4b46138d0f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 10V, Negative-QTOF	splash10-000i-0290000000-6c319e8337df67fc476d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 20V, Negative-QTOF	splash10-0006-1920000000-bfd50799ec0cb51b89fe	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 40V, Negative-QTOF	splash10-0fdo-9200000000-fe4583b38b03564abe97	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 10V, Positive-QTOF	splash10-0006-0190000000-57a11b44e9df0fc1d6a5	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 20V, Positive-QTOF	splash10-00xr-0690000000-b7a86bbaa7a707429283	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 40V, Positive-QTOF	splash10-002f-7900000000-0cb0aca82f0fb03cb603	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 10V, Negative-QTOF	splash10-00kf-0910000000-77790fad0fe8dd8e8a4e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 20V, Negative-QTOF	splash10-00kf-0900000000-0d38a13d09e7cb8e4809	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 6-Lactoyltetrahydropterin 40V, Negative-QTOF	splash10-0006-9500000000-81ba6afc34a8818ef29d	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm (predicted from logP)

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Pterine Biosynthesis
Dopa-responsive dystonia		Not Available
Hyperphenylalaniemia due to guanosine triphosphate cyclohydrolase deficiency		Not Available
Hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency (ptps)		Not Available
Hyperphenylalaninemia due to dhpr-deficiency		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022828

KNApSAcK ID

Not Available

Chemspider ID

148245

KEGG Compound ID

C04244

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

17248

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Milstien S, Kaufman S: Biosynthesis of tetrahydrobiopterin: conversion of dihydroneopterin triphosphate to tetrahydropterin intermediates. Biochem Biophys Res Commun. 1985 May 16;128(3):1099-107. [PubMed:4004850 ]
Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, Myers RH: Sepiapterin reductase expression is increased in Parkinson's disease brain tissue. Brain Res. 2007 Mar 30;1139:42-7. Epub 2007 Jan 8. [PubMed:17270157 ]

Enzymes

Enzyme Details

1. Sepiapterin reductase

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the final one or two reductions in tetra-hydrobiopterin biosynthesis to form 5,6,7,8-tetrahydrobiopterin.
Gene Name:: SPR
Uniprot ID:: P35270
Molecular weight:: 28048.13

Reactions

Tetrahydrobiopterin + NADP → 6-Lactoyltetrahydropterin + NADPH + Hydrogen Ion	details
6-Lactoyltetrahydropterin + NADP → Dyspropterin + NADPH + Hydrogen Ion	details

Showing metabocard for 6-Lactoyltetrahydropterin (HMDB0002065)

MOL for HMDB0002065 (6-Lactoyltetrahydropterin)

3D MOL for HMDB0002065 (6-Lactoyltetrahydropterin)

3D SDF for HMDB0002065 (6-Lactoyltetrahydropterin)

3D-SDF for HMDB0002065 (6-Lactoyltetrahydropterin)

PDB for HMDB0002065 (6-Lactoyltetrahydropterin)

3D PDB for HMDB0002065 (6-Lactoyltetrahydropterin)

SMILES for HMDB0002065 (6-Lactoyltetrahydropterin)

INCHI for HMDB0002065 (6-Lactoyltetrahydropterin)

Structure for HMDB0002065 (6-Lactoyltetrahydropterin)

3D Structure for HMDB0002065 (6-Lactoyltetrahydropterin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions