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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2006-05-22 14:17:32 UTC

Update Date

2021-09-14 15:46:58 UTC

HMDB ID

HMDB0002022

Secondary Accession Numbers

HMDB02022

Metabolite Identification

Common Name

Glycineamideribotide

Description

Glycineamideribotide, also known as GAR, belongs to the class of organic compounds known as glycinamide ribonucleotides. Glycinamide ribonucleotides are compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. Glycineamideribotide exists in all living species, ranging from bacteria to plants to humans. In humans, glycineamideribotide is involved in the metabolic disorder called the gout or kelley-seegmiller syndrome pathway. Glycineamideribotide has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make glycineamideribotide a potential biomarker for the consumption of these foods. Glycineamideribotide is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review very few articles have been published on Glycineamideribotide.

Structure

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

HMDB0002022
     RDKit          3D
Glycineamideribotide
 33 33  0  0  0  0  0  0  0  0999 V2000
   -5.1914   -2.8560    0.0864 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5905   -1.5615   -0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126   -1.6876   -0.1449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.7907    0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806   -0.5615   -0.3714 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416   -0.6537   -0.3483 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2688    0.2002    0.6014 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848    0.1094    0.2505 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9317    1.0844    1.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2497    0.9125    0.5953 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3100    1.9661    1.3949 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.6315    1.9523    0.6768 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5665    1.3751    2.9588 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6168    3.4920    1.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0257    0.5345   -1.2100 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1039    0.0538   -1.9386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2870   -0.1075   -1.6385 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0497   -1.1546   -2.5386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2033   -2.8258   -0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0239   -3.0577    1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9193   -1.1240   -1.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9532   -0.8827    0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    0.3656   -0.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4908   -1.6686   -0.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846   -0.9016    0.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8942    0.8757    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6239    2.1332    0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1406    0.4914    3.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    4.0624    2.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9538    1.6431   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8342    0.7146   -1.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495    0.6603   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -0.7928   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  5 23  1  0
  6 24  1  1
  8 25  1  6
  9 26  1  0
  9 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  1
 16 31  1  0
 17 32  1  6
 18 33  1  0
M  END


  Mrv1652306232018152D          

 18 18  0  0  0  0            999 V2000
10001.391910000.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.106710000.1508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.819410000.5628    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10002.409510001.2755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.534210000.1508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.233410001.2755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.8852 9998.7044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.627810000.5628    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.0941 9998.7126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.913810000.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.199910000.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.9138 9999.3263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.485710000.1508    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10000.006310000.6450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.338910000.1600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9999.5938 9999.3754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.4188 9999.3754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.673710000.1600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 11 13  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 15  1  0  0  0  0
 14 18  1  0  0  0  0
 18  1  1  6  0  0  0
 17  7  1  1  0  0  0
 15  8  1  6  0  0  0
 16  9  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0002022

> <DATABASE_NAME>
hmdb

> <SMILES>
NCC(=O)N[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C7H15N2O8P/c8-1-4(10)9-7-6(12)5(11)3(17-7)2-16-18(13,14)15/h3,5-7,11-12H,1-2,8H2,(H,9,10)(H2,13,14,15)/t3-,5-,6-,7-/m1/s1

> <INCHI_KEY>
OBQMLSFOUZUIOB-SHUUEZRQSA-N

> <FORMULA>
C7H15N2O8P

> <MOLECULAR_WEIGHT>
286.1764

> <EXACT_MASS>
286.056601978

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
23.677380162378174

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-5-(2-aminoacetamido)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-2.40

> <JCHEM_LOGP>
-4.650616976017661

> <ALOGPS_LOGS>
-1.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.245768050847792

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2255744528280514

> <JCHEM_PKA_STRONGEST_BASIC>
8.141960108603826

> <JCHEM_POLAR_SURFACE_AREA>
171.57000000000002

> <JCHEM_REFRACTIVITY>
55.2948

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.46e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
glycineamide ribonucleotide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0002022
     RDKit          3D
Glycineamideribotide
 33 33  0  0  0  0  0  0  0  0999 V2000
   -5.1914   -2.8560    0.0864 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5905   -1.5615   -0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126   -1.6876   -0.1449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.7907    0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806   -0.5615   -0.3714 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416   -0.6537   -0.3483 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2688    0.2002    0.6014 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848    0.1094    0.2505 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9317    1.0844    1.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2497    0.9125    0.5953 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3100    1.9661    1.3949 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.6315    1.9523    0.6768 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5665    1.3751    2.9588 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6168    3.4920    1.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0257    0.5345   -1.2100 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1039    0.0538   -1.9386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2870   -0.1075   -1.6385 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0497   -1.1546   -2.5386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2033   -2.8258   -0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0239   -3.0577    1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9193   -1.1240   -1.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9532   -0.8827    0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    0.3656   -0.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4908   -1.6686   -0.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846   -0.9016    0.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8942    0.8757    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6239    2.1332    0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1406    0.4914    3.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    4.0624    2.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9538    1.6431   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8342    0.7146   -1.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495    0.6603   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -0.7928   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  5 23  1  0
  6 24  1  1
  8 25  1  6
  9 26  1  0
  9 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  1
 16 31  1  0
 17 32  1  6
 18 33  1  0
M  END

HEADER    PROTEIN                                 23-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-JUN-20         0                                  
HETATM    1  C   UNK     0    8669.2658667.717   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0    8670.5998666.948   0.000  0.00  0.00           O+0
HETATM    3  P   UNK     0    8671.9308667.717   0.000  0.00  0.00           P+0
HETATM    4  O   UNK     0    8671.1648669.048   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0    8673.2648666.948   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8672.7028669.048   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0    8668.3198664.248   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0    8664.1058667.717   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0    8664.9768664.264   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    8662.7728666.948   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8661.4408667.717   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0    8662.7728665.409   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0    8660.1078666.948   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0    8666.6788667.871   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    8665.4338666.965   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8665.9088665.501   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8667.4488665.501   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8667.9248666.965   0.000  0.00  0.00           C+0
CONECT    1    2   18                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3                                                            
CONECT    7   17                                                            
CONECT    8   10   15                                                       
CONECT    9   16                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10   13                                                       
CONECT   12   10                                                            
CONECT   13   11                                                            
CONECT   14   15   18                                                       
CONECT   15   16   14    8                                                  
CONECT   16   15   17    9                                                  
CONECT   17   16   18    7                                                  
CONECT   18   17   14    1                                                  
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0002022
HETATM    1  N1  UNL     1      -5.191  -2.856   0.086  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.591  -1.562  -0.175  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.113  -1.688  -0.145  1.00  0.00           C  
HETATM    4  O1  UNL     1      -2.554  -2.791   0.081  1.00  0.00           O  
HETATM    5  N2  UNL     1      -2.281  -0.561  -0.371  1.00  0.00           N  
HETATM    6  C3  UNL     1      -0.842  -0.654  -0.348  1.00  0.00           C  
HETATM    7  O2  UNL     1      -0.269   0.200   0.601  1.00  0.00           O  
HETATM    8  C4  UNL     1       1.085   0.109   0.251  1.00  0.00           C  
HETATM    9  C5  UNL     1       1.932   1.084   1.017  1.00  0.00           C  
HETATM   10  O3  UNL     1       3.250   0.912   0.595  1.00  0.00           O  
HETATM   11  P1  UNL     1       4.310   1.966   1.395  1.00  0.00           P  
HETATM   12  O4  UNL     1       5.631   1.952   0.677  1.00  0.00           O  
HETATM   13  O5  UNL     1       4.567   1.375   2.959  1.00  0.00           O  
HETATM   14  O6  UNL     1       3.617   3.492   1.467  1.00  0.00           O  
HETATM   15  C6  UNL     1       1.026   0.534  -1.210  1.00  0.00           C  
HETATM   16  O7  UNL     1       2.104   0.054  -1.939  1.00  0.00           O  
HETATM   17  C7  UNL     1      -0.287  -0.107  -1.639  1.00  0.00           C  
HETATM   18  O8  UNL     1      -0.050  -1.155  -2.539  1.00  0.00           O  
HETATM   19  H1  UNL     1      -6.203  -2.826  -0.150  1.00  0.00           H  
HETATM   20  H2  UNL     1      -5.024  -3.058   1.109  1.00  0.00           H  
HETATM   21  H3  UNL     1      -4.919  -1.124  -1.141  1.00  0.00           H  
HETATM   22  H4  UNL     1      -4.953  -0.883   0.643  1.00  0.00           H  
HETATM   23  H5  UNL     1      -2.726   0.366  -0.561  1.00  0.00           H  
HETATM   24  H6  UNL     1      -0.491  -1.669  -0.141  1.00  0.00           H  
HETATM   25  H7  UNL     1       1.485  -0.902   0.366  1.00  0.00           H  
HETATM   26  H8  UNL     1       1.894   0.876   2.100  1.00  0.00           H  
HETATM   27  H9  UNL     1       1.624   2.133   0.819  1.00  0.00           H  
HETATM   28  H10 UNL     1       4.141   0.491   3.082  1.00  0.00           H  
HETATM   29  H11 UNL     1       3.969   4.062   2.183  1.00  0.00           H  
HETATM   30  H12 UNL     1       0.954   1.643  -1.245  1.00  0.00           H  
HETATM   31  H13 UNL     1       2.834   0.715  -1.952  1.00  0.00           H  
HETATM   32  H14 UNL     1      -0.949   0.660  -2.065  1.00  0.00           H  
HETATM   33  H15 UNL     1       0.021  -0.793  -3.461  1.00  0.00           H  
CONECT    1    2   19   20
CONECT    2    3   21   22
CONECT    3    4    4    5
CONECT    5    6   23
CONECT    6    7   17   24
CONECT    7    8
CONECT    8    9   15   25
CONECT    9   10   26   27
CONECT   10   11
CONECT   11   12   12   13   14
CONECT   13   28
CONECT   14   29
CONECT   15   16   17   30
CONECT   16   31
CONECT   17   18   32
CONECT   18   33
END

HMDB0002022
     RDKit          3D
Glycineamideribotide
 33 33  0  0  0  0  0  0  0  0999 V2000
   -5.1914   -2.8560    0.0864 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5905   -1.5615   -0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126   -1.6876   -0.1449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.7907    0.0811 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806   -0.5615   -0.3714 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8416   -0.6537   -0.3483 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2688    0.2002    0.6014 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848    0.1094    0.2505 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9317    1.0844    1.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2497    0.9125    0.5953 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3100    1.9661    1.3949 P   0  0  0  0  0  5  0  0  0  0  0  0
    5.6315    1.9523    0.6768 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5665    1.3751    2.9588 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6168    3.4920    1.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0257    0.5345   -1.2100 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1039    0.0538   -1.9386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2870   -0.1075   -1.6385 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0497   -1.1546   -2.5386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2033   -2.8258   -0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0239   -3.0577    1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9193   -1.1240   -1.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9532   -0.8827    0.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7260    0.3656   -0.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4908   -1.6686   -0.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846   -0.9016    0.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8942    0.8757    2.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6239    2.1332    0.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1406    0.4914    3.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    4.0624    2.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9538    1.6431   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8342    0.7146   -1.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495    0.6603   -2.0647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212   -0.7928   -3.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 11 14  1  0
  8 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17  6  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  5 23  1  0
  6 24  1  1
  8 25  1  6
  9 26  1  0
  9 27  1  0
 13 28  1  0
 14 29  1  0
 15 30  1  1
 16 31  1  0
 17 32  1  6
 18 33  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
GAR	Kegg
N1-(5-Phospho-D-ribosyl)glycinamide	Kegg
Glycinamide ribonucleotide	Kegg
N1-(5-Phospho-beta-D-ribosyl)glycinamide	Kegg
N1-(5-Phospho-b-D-ribosyl)glycinamide	Generator
N1-(5-Phospho-β-D-ribosyl)glycinamide	Generator
5'-Phosphoribosyl-glycineamide	HMDB
5'-Phosphoribosylglycinamide	HMDB
5'-Phosphoribosylglycineamide	HMDB
Glycineamide ribonucleotide	HMDB
N(1)-(5-phospho-D-Ribosyl)glycinamide	HMDB
N-Glycyl-5-O-phosphono-D-ribofuranosylamine	HMDB
2-Amino-N-(5-O-phosphono-beta-D-ribofuranosyl)acetamide	HMDB
2-Amino-N-(5-O-phosphono-β-D-ribofuranosyl)acetamide	HMDB
5-Phospho-beta-D-ribosyl-glycineamide	HMDB
5-Phospho-β-D-ribosyl-glycineamide	HMDB
5’-Phosphoribosylglycinamide	HMDB
5’-Phosphoribosylglycineamide	HMDB

Chemical Formula

C₇H₁₅N₂O₈P

Average Molecular Weight

286.1764

Monoisotopic Molecular Weight

286.056601978

IUPAC Name

{[(2R,3S,4R,5R)-5-(2-aminoacetamido)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

Traditional Name

glycineamide ribonucleotide

CAS Registry Number

10074-18-7

SMILES

NCC(=O)N[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C7H15N2O8P/c8-1-4(10)9-7-6(12)5(11)3(17-7)2-16-18(13,14)15/h3,5-7,11-12H,1-2,8H2,(H,9,10)(H2,13,14,15)/t3-,5-,6-,7-/m1/s1

InChI Key

OBQMLSFOUZUIOB-SHUUEZRQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycinamide ribonucleotides. Glycinamide ribonucleotides are compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Glycinamide ribonucleotides

Sub Class

Not Available

Direct Parent

Glycinamide ribonucleotides

Alternative Parents

Substituents

Glycinamide-ribonucleotide
Pentose phosphate
Pentose-5-phosphate
Alpha-amino acid amide
Alpha-amino acid or derivatives
Monosaccharide phosphate
Pentose monosaccharide
Monoalkyl phosphate
Monosaccharide
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Tetrahydrofuran
Secondary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
Carboxamide group
1,2-diol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxide
Primary aliphatic amine
Organopnictogen compound
Alcohol
Organonitrogen compound
Carbonyl group
Organooxygen compound
Amine
Organic oxygen compound
Hydrocarbon derivative
Primary amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB0002022)

Source

Endogenous

Endogenous (HMDB: HMDB0002022)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Purine Metabolism (HMDB: HMDB0002022)
One Carbon Pool by Folate (PathBank: SMP0001750)
One Carbon Pool by Folate I (PathBank: SMP0002369)

Azathioprine Action Pathway (HMDB: HMDB0002022)

Disease pathway

Adenosine Deaminase Deficiency (PathBank: SMP0000144)
Adenylosuccinate Lyase Deficiency (PathBank: SMP0000167)
Gout or Kelley-Seegmiller Syndrome (PathBank: SMP0000365)
Lesch-Nyhan Syndrome (LNS) (PathBank: SMP0000364)
Molybdenum Cofactor Deficiency (PathBank: SMP0000203)
Xanthine Dehydrogenase Deficiency (Xanthinuria) (PathBank: SMP0000220)
Purine Nucleoside Phosphorylase Deficiency (PathBank: SMP0000210)
AICA-Ribosiduria (PathBank: SMP0000168)
Xanthinuria Type I (PathBank: SMP0000512)
Xanthinuria Type II (PathBank: SMP0000513)
Adenine Phosphoribosyltransferase Deficiency (APRT) (PathBank: SMP0000535)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0000536)
Myoadenylate Deaminase Deficiency (PathBank: SMP0000537)
Mitochondrial DNA Depletion Syndrome (PathBank: SMP0120601)

Drug action pathway

Azathioprine Action Pathway (PathBank: SMP0000427)
Mercaptopurine Action Pathway (PathBank: SMP0000428)
Thioguanine Action Pathway (PathBank: SMP0000430)

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	14.6 g/L	ALOGPS
logP	-2.4	ALOGPS
logP	-4.7	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	1.23	ChemAxon
pKa (Strongest Basic)	8.14	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	171.57 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	55.29 m³·mol⁻¹	ChemAxon
Polarizability	23.68 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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]+	166.281	31661259
DarkChem	[M-H]-	160.137	31661259
DeepCCS	[M+H]+	154.685	30932474
DeepCCS	[M-H]-	152.289	30932474
DeepCCS	[M-2H]-	186.935	30932474
DeepCCS	[M+Na]+	161.792	30932474
AllCCS	[M+H]+	160.5	32859911
AllCCS	[M+H-H2O]+	157.2	32859911
AllCCS	[M+NH4]+	163.5	32859911
AllCCS	[M+Na]+	164.4	32859911
AllCCS	[M-H]-	155.9	32859911
AllCCS	[M+Na-2H]-	156.0	32859911
AllCCS	[M+HCOO]-	156.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Glycineamideribotide	NCC(=O)N[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	3149.2	Standard polar	33892256
Glycineamideribotide	NCC(=O)N[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	2341.3	Standard non polar	33892256
Glycineamideribotide	NCC(=O)N[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O	2690.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Glycineamideribotide,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN)[C@@H]1O	2520.9	Semi standard non polar	33892256
Glycineamideribotide,1TMS,isomer #2	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O)O)[C@H]1O	2526.3	Semi standard non polar	33892256
Glycineamideribotide,1TMS,isomer #3	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN)[C@H](O)[C@@H]1O	2579.3	Semi standard non polar	33892256
Glycineamideribotide,1TMS,isomer #4	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2569.2	Semi standard non polar	33892256
Glycineamideribotide,1TMS,isomer #5	C[Si](C)(C)N(C(=O)CN)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2447.3	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	2505.5	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #10	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@H](O)[C@@H]1O	2481.2	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #11	C[Si](C)(C)N(CC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C	2645.6	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #12	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C	2512.3	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	2589.3	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #3	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O	2565.1	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	2433.8	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2590.2	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #6	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C	2570.4	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN)[Si](C)(C)C	2446.6	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #8	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2611.5	Semi standard non polar	33892256
Glycineamideribotide,2TMS,isomer #9	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O	2620.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	2561.9	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	2394.0	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	4085.0	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #10	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2616.0	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #10	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2521.4	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #10	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3631.3	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	2476.0	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	2442.6	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	3870.5	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	2652.6	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	2691.3	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	3974.6	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #13	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2501.9	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #13	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2601.1	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #13	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	3932.6	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #14	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O	2627.7	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #14	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O	2542.8	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #14	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O	3454.4	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2503.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2472.4	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #15	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3735.0	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2742.7	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2668.4	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #16	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3729.2	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	2525.9	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	2574.3	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	3671.5	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #18	C[Si](C)(C)N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2628.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #18	C[Si](C)(C)N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2780.1	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #18	C[Si](C)(C)N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	4038.8	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2521.2	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2522.1	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3976.7	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2438.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2440.4	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4185.3	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	2604.2	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	2435.8	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	3878.9	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #5	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2611.1	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #5	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2520.6	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #5	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3651.4	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	2467.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	2444.2	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	3852.0	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2650.8	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2692.7	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	4010.6	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #8	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2495.7	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #8	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2604.9	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #8	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	3920.2	Standard polar	33892256
Glycineamideribotide,3TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2602.7	Semi standard non polar	33892256
Glycineamideribotide,3TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2436.6	Standard non polar	33892256
Glycineamideribotide,3TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	3867.1	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	2608.2	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	2420.5	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C	3738.5	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2600.9	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2746.2	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3665.2	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #11	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2664.7	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #11	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	2552.8	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #11	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C	3170.2	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	2497.3	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	2444.5	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #12	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C	3501.5	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #13	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2722.8	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #13	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	2660.2	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #13	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@H]1O	3419.6	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #14	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2534.6	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #14	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2560.1	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #14	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	3366.0	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2610.2	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2746.1	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3662.6	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2743.0	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2684.2	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #16	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3295.5	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	2549.1	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	2573.8	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #17	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C	3216.6	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2664.0	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	2717.5	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #18	C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O	3487.8	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2604.9	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2518.1	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #2	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3395.4	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2473.2	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2433.9	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3691.9	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2612.3	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2663.7	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3674.9	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #5	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2483.5	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #5	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2592.6	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #5	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	3596.4	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #6	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2653.0	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #6	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	2545.1	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #6	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O	3179.2	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	2499.8	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	2442.5	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #7	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O	3481.0	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2715.7	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2650.9	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3453.4	Standard polar	33892256
Glycineamideribotide,4TMS,isomer #9	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2544.9	Semi standard non polar	33892256
Glycineamideribotide,4TMS,isomer #9	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2565.4	Standard non polar	33892256
Glycineamideribotide,4TMS,isomer #9	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	3352.1	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #1	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2668.7	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #1	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	2535.6	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #1	C[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3005.9	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #10	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2563.9	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #10	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2561.1	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #10	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2986.4	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2669.1	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2683.7	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3198.4	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2697.6	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	2695.4	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #12	C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C	3107.5	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2497.3	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2432.2	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3405.0	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2692.8	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2643.5	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3208.2	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #4	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2529.7	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #4	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2560.1	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #4	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	3127.0	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2587.8	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2724.2	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3350.4	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2738.6	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2654.5	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #6	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3062.1	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #7	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2577.2	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #7	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2559.0	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #7	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)[Si](C)(C)C	2966.2	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2666.9	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2687.8	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	3198.1	Standard polar	33892256
Glycineamideribotide,5TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2741.2	Semi standard non polar	33892256
Glycineamideribotide,5TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	2670.1	Standard non polar	33892256
Glycineamideribotide,5TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@H]1O	3044.3	Standard polar	33892256
Glycineamideribotide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2717.8	Semi standard non polar	33892256
Glycineamideribotide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2647.4	Standard non polar	33892256
Glycineamideribotide,6TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2918.4	Standard polar	33892256
Glycineamideribotide,6TMS,isomer #2	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2569.0	Semi standard non polar	33892256
Glycineamideribotide,6TMS,isomer #2	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2559.8	Standard non polar	33892256
Glycineamideribotide,6TMS,isomer #2	C[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C	2830.7	Standard polar	33892256
Glycineamideribotide,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2655.7	Semi standard non polar	33892256
Glycineamideribotide,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2677.1	Standard non polar	33892256
Glycineamideribotide,6TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3008.6	Standard polar	33892256
Glycineamideribotide,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2710.0	Semi standard non polar	33892256
Glycineamideribotide,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2665.0	Standard non polar	33892256
Glycineamideribotide,6TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O	2890.8	Standard polar	33892256
Glycineamideribotide,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2708.0	Semi standard non polar	33892256
Glycineamideribotide,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2669.3	Standard non polar	33892256
Glycineamideribotide,6TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2901.9	Standard polar	33892256
Glycineamideribotide,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2703.3	Semi standard non polar	33892256
Glycineamideribotide,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2676.9	Standard non polar	33892256
Glycineamideribotide,7TMS,isomer #1	C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2804.1	Standard polar	33892256
Glycineamideribotide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN)[C@@H]1O	2772.7	Semi standard non polar	33892256
Glycineamideribotide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O)O)[C@H]1O	2767.2	Semi standard non polar	33892256
Glycineamideribotide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN)[C@H](O)[C@@H]1O	2831.8	Semi standard non polar	33892256
Glycineamideribotide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2786.9	Semi standard non polar	33892256
Glycineamideribotide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C(=O)CN)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	2688.8	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	2936.5	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	2931.3	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(CC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3078.1	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	2940.6	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	3034.6	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	2963.8	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	2877.7	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3035.1	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	2969.0	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	2877.4	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3057.4	Semi standard non polar	33892256
Glycineamideribotide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3070.7	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	3218.1	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	2973.7	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	4098.7	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3262.8	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3101.2	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3743.4	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3113.7	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3004.0	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3937.9	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	3260.5	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	3236.8	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O)[C@H]1O	3989.7	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3135.2	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3164.1	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3953.1	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3298.9	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3098.7	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O	3617.7	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3139.0	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	2987.0	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3825.3	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3344.3	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3205.9	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3832.7	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3200.2	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3143.9	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3775.5	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	3244.4	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	3300.8	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O	4032.9	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3154.0	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3115.4	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3993.2	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3072.5	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3025.7	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4201.3	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	3240.3	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	2966.7	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O	3915.7	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3269.5	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3098.9	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3756.1	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3115.8	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3004.0	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3921.2	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3260.1	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3235.4	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	4013.9	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3132.9	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3163.0	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3945.6	Standard polar	33892256
Glycineamideribotide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3233.2	Semi standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	2968.7	Standard non polar	33892256
Glycineamideribotide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3911.6	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	3436.5	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	3081.8	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN)[C@@H]1O[Si](C)(C)C(C)(C)C	3789.1	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3435.8	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3420.5	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3746.6	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3478.0	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3221.1	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3450.3	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3318.9	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3092.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN)[Si](C)(C)C(C)(C)C	3667.9	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3561.0	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3351.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@H]1O	3576.7	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3378.3	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3254.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3558.5	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3429.5	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3415.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3746.8	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3588.5	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3343.7	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3522.3	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3409.0	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3237.3	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)[Si](C)(C)C(C)(C)C	3483.2	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3493.0	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3395.4	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	3645.1	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3444.0	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3215.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3581.2	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3322.9	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3119.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3796.7	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3467.5	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3361.4	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3744.4	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3329.9	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3290.8	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3705.9	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3488.7	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3212.2	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3448.0	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3328.9	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3088.2	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O	3648.3	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3565.5	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3344.0	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3598.0	Standard polar	33892256
Glycineamideribotide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3381.6	Semi standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3260.6	Standard non polar	33892256
Glycineamideribotide,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3551.5	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3655.9	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3304.5	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NCC(=O)N[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3383.2	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3567.6	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3324.2	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3372.7	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3679.3	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3492.4	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3483.5	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3712.3	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3471.8	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C	3432.8	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3513.4	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3194.1	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3636.8	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3750.7	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3449.4	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3482.8	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3560.0	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3364.1	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3450.4	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3643.6	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3534.7	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3586.8	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3790.6	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3434.5	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3388.6	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3581.6	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3324.8	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NCC(=O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)[Si](C)(C)C(C)(C)C	3356.2	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3690.1	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3501.2	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N(C(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H]1O	3481.1	Standard polar	33892256
Glycineamideribotide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3775.9	Semi standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3450.6	Standard non polar	33892256
Glycineamideribotide,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](NC(=O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H]1O	3384.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Glycineamideribotide GC-MS (Non-derivatized) - 70eV, Positive	splash10-000t-9420000000-d7fee78dd4657e2eba28	2016-09-22	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glycineamideribotide GC-MS (2 TMS) - 70eV, Positive	splash10-00si-9541200000-4a23e3091baf72b01dc2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glycineamideribotide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - Glycineamideribotide 10V, Positive-QTOF	splash10-053i-9460000000-f71dc4d8ec0f4da03819	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 20V, Positive-QTOF	splash10-0560-9120000000-4770933b45387be6728c	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 40V, Positive-QTOF	splash10-0a59-9200000000-a6f2b9ab201fd0e69ee8	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 10V, Negative-QTOF	splash10-0170-9550000000-99520656892b8c415efb	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 20V, Negative-QTOF	splash10-004i-9000000000-d6c860661b01956c80ac	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 40V, Negative-QTOF	splash10-004i-9000000000-c2f2b85e6ec9caaa4408	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 10V, Negative-QTOF	splash10-002r-2090000000-f6fcd99577c7e5d5d2ec	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 20V, Negative-QTOF	splash10-004i-9020000000-f5f361d4aef59382fc15	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 40V, Negative-QTOF	splash10-004i-9000000000-962cd48ee45a1c95e446	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 10V, Positive-QTOF	splash10-000i-0980000000-6a9e014a86b77c5ad3c3	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 20V, Positive-QTOF	splash10-001i-5920000000-cb0c5e3520ad275d3742	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glycineamideribotide 40V, Positive-QTOF	splash10-057j-9500000000-ab2ea8c5eb8a25044810	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	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
Purine metabolism	Not Available
Adenosine Deaminase Deficiency		Not Available
Adenylosuccinate Lyase Deficiency		Not Available
Gout or Kelley-Seegmiller Syndrome		Not Available
Lesch-Nyhan Syndrome (LNS)		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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

5-PHOSPHO-RIBOSYL-GLYCINEAMIDE

BiGG ID

42621

Wikipedia Link

Glycineamide ribonucleotide

METLIN ID

Not Available

PubChem Compound

160913

PDB ID

Not Available

ChEBI ID

18349

Food Biomarker Ontology

Not Available

VMH ID

GAR

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Caperelli CA, Giroux EL: The human glycinamide ribonucleotide transformylase domain: purification, characterization, and kinetic mechanism. Arch Biochem Biophys. 1997 May 1;341(1):98-103. [PubMed:9143358 ]
McKerns KW: Gonadotropin regulation of nucleotide biosynthesis in corpus luteum. Biochemistry. 1973 Dec 4;12(25):5206-11. [PubMed:4366083 ]

Enzymes

Enzyme Details

1. Trifunctional purine biosynthetic protein adenosine-3

General function:: Involved in catalytic activity
Specific function:: Not Available
Gene Name:: GART
Uniprot ID:: P22102
Molecular weight:: 107766.295

Reactions

Adenosine triphosphate + 5-Phosphoribosylamine + Glycine → ADP + Phosphate + Glycineamideribotide	details
10-Formyltetrahydrofolate + Glycineamideribotide → Tetrahydrofolic acid + N(2)-formyl-N(1)-(5-phospho-D-ribosyl)glycinamide	details
Adenosine triphosphate + 5-Phosphoribosylamine + Glycine → ADP + Phosphate + Glycineamideribotide	details
10-Formyltetrahydrofolate + Glycineamideribotide → Tetrahydrofolic acid + 5'-Phosphoribosyl-N-formylglycinamide	details
Glycineamideribotide + 5,10-Methenyltetrahydrofolic acid + Water → 5'-Phosphoribosyl-N-formylglycinamide + Tetrahydrofolic acid	details

Showing metabocard for Glycineamideribotide (HMDB0002022)

MOL for HMDB0002022 (Glycineamideribotide)

3D MOL for HMDB0002022 (Glycineamideribotide)

3D SDF for HMDB0002022 (Glycineamideribotide)

3D-SDF for HMDB0002022 (Glycineamideribotide)

PDB for HMDB0002022 (Glycineamideribotide)

3D PDB for HMDB0002022 (Glycineamideribotide)

SMILES for HMDB0002022 (Glycineamideribotide)

INCHI for HMDB0002022 (Glycineamideribotide)

Structure for HMDB0002022 (Glycineamideribotide)

3D Structure for HMDB0002022 (Glycineamideribotide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions