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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2009-01-08 17:23:30 UTC

Update Date

2022-11-30 19:03:59 UTC

HMDB ID

HMDB0011500

Secondary Accession Numbers

HMDB11500

Metabolite Identification

Common Name

LysoPE(14:0/0:0)

Description

LysoPE(14:0/0:0) is a lysophosphatidylethanolamine or a lysophospholipid. The term 'lysophospholipid' (LPL) refers to any phospholipid that is missing one of its two O-acyl chains. Thus, LPLs have a free alcohol in either the sn-1 or sn-2 position. The prefix 'lyso-' comes from the fact that lysophospholipids were originally found to be hemolytic however it is now used to refer generally to phospholipids missing an acyl chain. LPLs are usually the result of phospholipase A-type enzymatic activity on regular phospholipids such as phosphatidylcholine or phosphatidic acid, although they can also be generated by the acylation of glycerophospholipids or the phosphorylation of monoacylglycerols. Some LPLs serve important signaling functions such as lysophosphatidic acid. Lysophosphatidylethanolamines (LPEs) can function as plant growth regulators with several diverse uses. (LPEs) are approved for outdoor agricultural use to accelerate ripening and improve the quality of fresh produce. They are also approved for indoor use to preserve stored crops and commercial cut flowers. As a breakdown product of phosphatidylethanolamine (PE), LPE is present in cells of all organisms.

Structure

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


  Mrv0541 02241201422D          

 29 28  0  0  1  0            999 V2000
   23.0867  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4117  -12.0914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.7365  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7619  -12.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0614  -12.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8848  -12.8710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.4370  -11.7016    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   24.0472  -11.0264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8268  -12.3767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.1121  -11.3118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7872  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4623  -11.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1375  -11.7016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.9994  -12.9007    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0587  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7732  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4876  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2021  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9166  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6311  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3456  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0600  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7745  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4890  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2034  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9179  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6324  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3469  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3469  -10.8539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28  5  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

HMDB0011500
     RDKit          3D
LysoPE(14:0/0:0)
 68 67  0  0  0  0  0  0  0  0999 V2000
   -9.3763   -1.5530   -0.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8374   -1.5348   -0.4312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5101   -0.1481   -0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7403    0.9651   -0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6385    1.6179    0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5992    2.3633    0.0185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.7131   -0.9097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8882    0.5885   -0.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1136    1.1189    0.9141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4850   -0.0604    1.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -0.9250    0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2894   -0.4242    0.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0741    0.7793   -0.4240 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5264    0.8819   -0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9993    1.4550   -1.3724 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1342    0.2973    0.5980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4301    0.0950    0.9835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1175   -0.8214    0.0317 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9076   -0.2586   -1.2763 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6647   -0.8043    0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1951   -1.5024   -0.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7253   -1.0451   -1.0911 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.9600   -1.0888   -2.6915 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9070    0.6695   -0.7808 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0385   -1.8245   -0.5179 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6524   -1.0521    0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0777   -0.7938    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8045   -0.0087    1.0113 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7348   -2.5677   -0.3552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7763   -0.8501   -0.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5825   -1.1970    0.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2596   -1.9002    0.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6602   -2.2184   -1.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4447   -0.2462   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1023    0.0080   -1.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3996    0.4646    0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4786    1.7484   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2396    0.9884    1.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1874    2.4323    1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9718    2.9943    0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1352    3.1864   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8908    2.4839   -1.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1438    1.3970   -1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806    0.3231   -1.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4384   -0.3329   -0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8577    1.5449    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4089    1.8740    0.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9178    0.2778    2.4988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3010   -0.7326    1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517   -1.8283    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0988   -1.4899   -0.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3208   -1.2407   -0.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.2973    1.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3250    0.6400   -1.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3331    1.7456   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0079    1.0449    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979   -0.4144    2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -1.8436   -0.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3389   -0.9280   -1.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7914   -1.4770    1.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489    0.1865    0.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0359    1.0919   -1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0256   -0.2339    0.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7113   -1.7739    1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0067   -0.1117   -0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6127   -1.6445   -0.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3530    0.8381    1.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9576   -0.6411    1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  6
 19 59  1  0
 20 60  1  0
 20 61  1  0
 24 62  1  0
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
M  END


  Mrv0541 02241201422D          

 29 28  0  0  1  0            999 V2000
   23.0867  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4117  -12.0914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.7365  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7619  -12.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0614  -12.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8848  -12.8710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.4370  -11.7016    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   24.0472  -11.0264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.8268  -12.3767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.1121  -11.3118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7872  -11.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4623  -11.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1375  -11.7016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.9994  -12.9007    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0587  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7732  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4876  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2021  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9166  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6311  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3456  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0600  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7745  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4890  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2034  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9179  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6324  -12.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3469  -11.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3469  -10.8539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28  5  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011500

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](O)(COC(=O)CCCCCCCCCCCCC)COP(O)(=O)OCCN

> <INCHI_IDENTIFIER>
InChI=1S/C19H40NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-19(22)25-16-18(21)17-27-28(23,24)26-15-14-20/h18,21H,2-17,20H2,1H3,(H,23,24)/t18-/m1/s1

> <INCHI_KEY>
RPXHXZNGZBHSMJ-GOSISDBHSA-N

> <FORMULA>
C19H40NO7P

> <MOLECULAR_WEIGHT>
425.4972

> <EXACT_MASS>
425.254239151

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
47.96872670249316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2-aminoethoxy)[(2R)-2-hydroxy-3-(tetradecanoyloxy)propoxy]phosphinic acid

> <ALOGPS_LOGP>
3.25

> <JCHEM_LOGP>
2.6407240964756653

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.655705215902849

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8690837557474262

> <JCHEM_PKA_STRONGEST_BASIC>
9.999833383834863

> <JCHEM_POLAR_SURFACE_AREA>
128.31

> <JCHEM_REFRACTIVITY>
108.21049999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
21

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy(2R)-2-hydroxy-3-(tetradecanoyloxy)propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011500
     RDKit          3D
LysoPE(14:0/0:0)
 68 67  0  0  0  0  0  0  0  0999 V2000
   -9.3763   -1.5530   -0.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8374   -1.5348   -0.4312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5101   -0.1481   -0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7403    0.9651   -0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6385    1.6179    0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5992    2.3633    0.0185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.7131   -0.9097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8882    0.5885   -0.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1136    1.1189    0.9141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4850   -0.0604    1.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -0.9250    0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2894   -0.4242    0.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0741    0.7793   -0.4240 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5264    0.8819   -0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9993    1.4550   -1.3724 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1342    0.2973    0.5980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4301    0.0950    0.9835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1175   -0.8214    0.0317 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9076   -0.2586   -1.2763 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6647   -0.8043    0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1951   -1.5024   -0.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7253   -1.0451   -1.0911 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.9600   -1.0888   -2.6915 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9070    0.6695   -0.7808 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0385   -1.8245   -0.5179 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6524   -1.0521    0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0777   -0.7938    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8045   -0.0087    1.0113 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7348   -2.5677   -0.3552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7763   -0.8501   -0.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5825   -1.1970    0.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2596   -1.9002    0.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6602   -2.2184   -1.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4447   -0.2462   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1023    0.0080   -1.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3996    0.4646    0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4786    1.7484   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2396    0.9884    1.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1874    2.4323    1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9718    2.9943    0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1352    3.1864   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8908    2.4839   -1.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1438    1.3970   -1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806    0.3231   -1.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4384   -0.3329   -0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8577    1.5449    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4089    1.8740    0.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9178    0.2778    2.4988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3010   -0.7326    1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517   -1.8283    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0988   -1.4899   -0.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3208   -1.2407   -0.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.2973    1.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3250    0.6400   -1.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3331    1.7456   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0079    1.0449    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979   -0.4144    2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -1.8436   -0.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3389   -0.9280   -1.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7914   -1.4770    1.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489    0.1865    0.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0359    1.0919   -1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0256   -0.2339    0.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7113   -1.7739    1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0067   -0.1117   -0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6127   -1.6445   -0.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3530    0.8381    1.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9576   -0.6411    1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  6
 19 59  1  0
 20 60  1  0
 20 61  1  0
 24 62  1  0
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      43.095 -21.843   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      41.835 -22.571   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      40.575 -21.843   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      44.356 -22.571   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      39.315 -22.571   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      40.852 -24.026   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      45.616 -21.843   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      44.888 -20.583   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      46.343 -23.103   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      46.876 -21.115   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      48.136 -21.843   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      49.396 -21.115   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      50.657 -21.843   0.000  0.00  0.00           N+0
HETATM   14  H   UNK     0      42.932 -24.081   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0      20.643 -22.571   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.977 -21.801   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.310 -22.571   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.644 -21.801   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      25.978 -22.571   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      27.311 -21.801   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      28.645 -22.571   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      29.979 -21.801   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      31.312 -22.571   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      32.646 -21.801   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      33.980 -22.571   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      35.313 -21.801   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      36.647 -22.571   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      37.981 -21.801   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      37.981 -20.261   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   14                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3   28                                                       
CONECT    6    2                                                            
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    2                                                            
CONECT   15   16                                                            
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    5   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   56    0
END

COMPND    HMDB0011500
HETATM    1  C1  UNL     1      -9.376  -1.553  -0.195  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.837  -1.535  -0.431  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.510  -0.148  -0.931  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.740   0.965  -0.021  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.639   1.618   0.739  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.599   2.363   0.018  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.688   1.713  -0.910  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.888   0.588  -0.277  1.00  0.00           C  
HETATM    9  C9  UNL     1      -3.114   1.119   0.914  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.485  -0.060   1.578  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.563  -0.925   0.813  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.289  -0.424   0.422  1.00  0.00           C  
HETATM   13  C13 UNL     1      -0.074   0.779  -0.424  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.526   0.882  -0.453  1.00  0.00           C  
HETATM   15  O1  UNL     1       1.999   1.455  -1.372  1.00  0.00           O  
HETATM   16  O2  UNL     1       2.134   0.297   0.598  1.00  0.00           O  
HETATM   17  C15 UNL     1       3.430   0.095   0.983  1.00  0.00           C  
HETATM   18  C16 UNL     1       4.118  -0.821   0.032  1.00  0.00           C  
HETATM   19  O3  UNL     1       3.908  -0.259  -1.276  1.00  0.00           O  
HETATM   20  C17 UNL     1       5.665  -0.804   0.232  1.00  0.00           C  
HETATM   21  O4  UNL     1       6.195  -1.502  -0.840  1.00  0.00           O  
HETATM   22  P1  UNL     1       7.725  -1.045  -1.091  1.00  0.00           P  
HETATM   23  O5  UNL     1       7.960  -1.089  -2.691  1.00  0.00           O  
HETATM   24  O6  UNL     1       7.907   0.670  -0.781  1.00  0.00           O  
HETATM   25  O7  UNL     1       9.038  -1.825  -0.518  1.00  0.00           O  
HETATM   26  C18 UNL     1       9.652  -1.052   0.482  1.00  0.00           C  
HETATM   27  C19 UNL     1      11.078  -0.794   0.017  1.00  0.00           C  
HETATM   28  N1  UNL     1      11.805  -0.009   1.011  1.00  0.00           N  
HETATM   29  H1  UNL     1      -9.735  -2.568  -0.355  1.00  0.00           H  
HETATM   30  H2  UNL     1      -9.776  -0.850  -0.992  1.00  0.00           H  
HETATM   31  H3  UNL     1      -9.583  -1.197   0.809  1.00  0.00           H  
HETATM   32  H4  UNL     1      -7.260  -1.900   0.388  1.00  0.00           H  
HETATM   33  H5  UNL     1      -7.660  -2.218  -1.338  1.00  0.00           H  
HETATM   34  H6  UNL     1      -6.445  -0.246  -1.288  1.00  0.00           H  
HETATM   35  H7  UNL     1      -8.102   0.008  -1.865  1.00  0.00           H  
HETATM   36  H8  UNL     1      -8.400   0.465   0.831  1.00  0.00           H  
HETATM   37  H9  UNL     1      -8.479   1.748  -0.351  1.00  0.00           H  
HETATM   38  H10 UNL     1      -6.240   0.988   1.556  1.00  0.00           H  
HETATM   39  H11 UNL     1      -7.187   2.432   1.357  1.00  0.00           H  
HETATM   40  H12 UNL     1      -4.972   2.994   0.759  1.00  0.00           H  
HETATM   41  H13 UNL     1      -6.135   3.186  -0.550  1.00  0.00           H  
HETATM   42  H14 UNL     1      -3.891   2.484  -1.226  1.00  0.00           H  
HETATM   43  H15 UNL     1      -5.144   1.397  -1.840  1.00  0.00           H  
HETATM   44  H16 UNL     1      -3.081   0.323  -1.017  1.00  0.00           H  
HETATM   45  H17 UNL     1      -4.438  -0.333  -0.095  1.00  0.00           H  
HETATM   46  H18 UNL     1      -3.858   1.545   1.672  1.00  0.00           H  
HETATM   47  H19 UNL     1      -2.409   1.874   0.681  1.00  0.00           H  
HETATM   48  H20 UNL     1      -1.918   0.278   2.499  1.00  0.00           H  
HETATM   49  H21 UNL     1      -3.301  -0.733   1.994  1.00  0.00           H  
HETATM   50  H22 UNL     1      -1.352  -1.828   1.522  1.00  0.00           H  
HETATM   51  H23 UNL     1      -2.099  -1.490  -0.015  1.00  0.00           H  
HETATM   52  H24 UNL     1       0.321  -1.241  -0.154  1.00  0.00           H  
HETATM   53  H25 UNL     1       0.404  -0.297   1.340  1.00  0.00           H  
HETATM   54  H26 UNL     1      -0.325   0.640  -1.475  1.00  0.00           H  
HETATM   55  H27 UNL     1      -0.333   1.746  -0.036  1.00  0.00           H  
HETATM   56  H28 UNL     1       4.008   1.045   1.105  1.00  0.00           H  
HETATM   57  H29 UNL     1       3.398  -0.414   2.005  1.00  0.00           H  
HETATM   58  H30 UNL     1       3.770  -1.844  -0.017  1.00  0.00           H  
HETATM   59  H31 UNL     1       3.339  -0.928  -1.765  1.00  0.00           H  
HETATM   60  H32 UNL     1       5.791  -1.477   1.159  1.00  0.00           H  
HETATM   61  H33 UNL     1       6.049   0.187   0.378  1.00  0.00           H  
HETATM   62  H34 UNL     1       7.036   1.092  -1.119  1.00  0.00           H  
HETATM   63  H35 UNL     1       9.026  -0.234   0.744  1.00  0.00           H  
HETATM   64  H36 UNL     1       9.711  -1.774   1.376  1.00  0.00           H  
HETATM   65  H37 UNL     1      11.007  -0.112  -0.934  1.00  0.00           H  
HETATM   66  H38 UNL     1      11.613  -1.645  -0.347  1.00  0.00           H  
HETATM   67  H39 UNL     1      11.353   0.838   1.311  1.00  0.00           H  
HETATM   68  H40 UNL     1      11.958  -0.641   1.808  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3   32   33
CONECT    3    4   34   35
CONECT    4    5   36   37
CONECT    5    6   38   39
CONECT    6    7   40   41
CONECT    7    8   42   43
CONECT    8    9   44   45
CONECT    9   10   46   47
CONECT   10   11   48   49
CONECT   11   12   50   51
CONECT   12   13   52   53
CONECT   13   14   54   55
CONECT   14   15   15   16
CONECT   16   17
CONECT   17   18   56   57
CONECT   18   19   20   58
CONECT   19   59
CONECT   20   21   60   61
CONECT   21   22
CONECT   22   23   23   24   25
CONECT   24   62
CONECT   25   26
CONECT   26   27   63   64
CONECT   27   28   65   66
CONECT   28   67   68
END

HMDB0011500
     RDKit          3D
LysoPE(14:0/0:0)
 68 67  0  0  0  0  0  0  0  0999 V2000
   -9.3763   -1.5530   -0.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8374   -1.5348   -0.4312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5101   -0.1481   -0.9308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7403    0.9651   -0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6385    1.6179    0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5992    2.3633    0.0185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.7131   -0.9097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8882    0.5885   -0.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1136    1.1189    0.9141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4850   -0.0604    1.5780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5632   -0.9250    0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2894   -0.4242    0.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0741    0.7793   -0.4240 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5264    0.8819   -0.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9993    1.4550   -1.3724 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1342    0.2973    0.5980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4301    0.0950    0.9835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1175   -0.8214    0.0317 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9076   -0.2586   -1.2763 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6647   -0.8043    0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1951   -1.5024   -0.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7253   -1.0451   -1.0911 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.9600   -1.0888   -2.6915 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9070    0.6695   -0.7808 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0385   -1.8245   -0.5179 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6524   -1.0521    0.4819 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0777   -0.7938    0.0168 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8045   -0.0087    1.0113 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7348   -2.5677   -0.3552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7763   -0.8501   -0.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5825   -1.1970    0.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2596   -1.9002    0.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6602   -2.2184   -1.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4447   -0.2462   -1.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1023    0.0080   -1.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3996    0.4646    0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4786    1.7484   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2396    0.9884    1.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1874    2.4323    1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9718    2.9943    0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1352    3.1864   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8908    2.4839   -1.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1438    1.3970   -1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0806    0.3231   -1.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4384   -0.3329   -0.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8577    1.5449    1.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4089    1.8740    0.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9178    0.2778    2.4988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3010   -0.7326    1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3517   -1.8283    1.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0988   -1.4899   -0.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3208   -1.2407   -0.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.2973    1.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3250    0.6400   -1.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3331    1.7456   -0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0079    1.0449    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979   -0.4144    2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -1.8436   -0.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3389   -0.9280   -1.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7914   -1.4770    1.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0489    0.1865    0.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0359    1.0919   -1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0256   -0.2339    0.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7113   -1.7739    1.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0067   -0.1117   -0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6127   -1.6445   -0.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3530    0.8381    1.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9576   -0.6411    1.8076 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  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  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  0
 13 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  6
 19 59  1  0
 20 60  1  0
 20 61  1  0
 24 62  1  0
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-Tetradecanoyl-sn-glycero-3-phosphoethanolamine	ChEBI
1-Tetradecanoyl-sn-glycero-3-phosphoethanolamine zwitterion	ChEBI
LPE (14:0/0:0)	ChEBI
1-Myristoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine	HMDB
LPE(14:0)	HMDB
LPE(14:0/0:0)	HMDB
Lyso-pe(14:0)	HMDB
Lyso-pe(14:0/0:0)	HMDB
LysoPE(14:0)	HMDB
Lysophosphatidylethanolamine(14:0)	HMDB
Lysophosphatidylethanolamine(14:0/0:0)	HMDB
Tetradecanoyl-lysophosphatidylethanolamine	HMDB
1-Tetradecanoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine	HMDB
1-Tetradecanoylglycerophosphoethanolamine	HMDB
LysoPE(14:0/0:0)	Lipid Annotator

Chemical Formula

C₁₉H₄₀NO₇P

Average Molecular Weight

425.4972

Monoisotopic Molecular Weight

425.254239151

IUPAC Name

(2-aminoethoxy)[(2R)-2-hydroxy-3-(tetradecanoyloxy)propoxy]phosphinic acid

Traditional Name

2-aminoethoxy(2R)-2-hydroxy-3-(tetradecanoyloxy)propoxyphosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](O)(COC(=O)CCCCCCCCCCCCC)COP(O)(=O)OCCN

InChI Identifier

InChI=1S/C19H40NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-19(22)25-16-18(21)17-27-28(23,24)26-15-14-20/h18,21H,2-17,20H2,1H3,(H,23,24)/t18-/m1/s1

InChI Key

RPXHXZNGZBHSMJ-GOSISDBHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-acyl-sn-glycero-3-phosphoethanolamines. These are glycerophoethanolamines in which the glycerol is esterified with a fatty acid at O-1 position, and linked at position 3 to a phosphoethanolamine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoethanolamines

Direct Parent

1-acyl-sn-glycero-3-phosphoethanolamines

Alternative Parents

Substituents

1-monoacyl-sn-glycero-3-phosphoethanolamine
Phosphoethanolamine
Fatty acid ester
Dialkyl phosphate
Organic phosphoric acid derivative
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Amino acid or derivatives
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Amine
Organooxygen compound
Primary amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

1-acyl-sn-glycero-3-phosphoethanolamine (CHEBI:85215 )
Monoacylglycerophosphoethanolamines (LMGP02050003 )

Ontology

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	0.0071 g/L	ALOGPS
logP	3.25	ALOGPS
logP	2.64	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	1.87	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	128.31 Å²	ChemAxon
Rotatable Bond Count	21	ChemAxon
Refractivity	108.21 m³·mol⁻¹	ChemAxon
Polarizability	47.97 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	207.194	31661259
DarkChem	[M-H]-	202.087	31661259
DeepCCS	[M+H]+	185.38	30932474
DeepCCS	[M-H]-	181.717	30932474
DeepCCS	[M-2H]-	218.665	30932474
DeepCCS	[M+Na]+	194.415	30932474
AllCCS	[M+H]+	206.2	32859911
AllCCS	[M+H-H2O]+	204.2	32859911
AllCCS	[M+NH4]+	208.0	32859911
AllCCS	[M+Na]+	208.5	32859911
AllCCS	[M-H]-	203.8	32859911
AllCCS	[M+Na-2H]-	205.6	32859911
AllCCS	[M+HCOO]-	207.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
LysoPE(14:0/0:0)	[H][C@@](O)(COC(=O)CCCCCCCCCCCCC)COP(O)(=O)OCCN	3366.1	Standard polar	33892256
LysoPE(14:0/0:0)	[H][C@@](O)(COC(=O)CCCCCCCCCCCCC)COP(O)(=O)OCCN	2970.1	Standard non polar	33892256
LysoPE(14:0/0:0)	[H][C@@](O)(COC(=O)CCCCCCCCCCCCC)COP(O)(=O)OCCN	3186.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
LysoPE(14:0/0:0),1TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN)O[Si](C)(C)C	3157.7	Semi standard non polar	33892256
LysoPE(14:0/0:0),1TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN)O[Si](C)(C)C	3137.1	Semi standard non polar	33892256
LysoPE(14:0/0:0),1TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN[Si](C)(C)C	3215.9	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)O[Si](C)(C)C	3165.5	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)O[Si](C)(C)C	3008.7	Standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C)O[Si](C)(C)C	4557.7	Standard polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)O[Si](C)(C)C	3236.1	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)O[Si](C)(C)C	3159.3	Standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C)O[Si](C)(C)C	4485.3	Standard polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3242.0	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3170.6	Standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C	3931.2	Standard polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3413.8	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	3197.7	Standard non polar	33892256
LysoPE(14:0/0:0),2TMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C	4518.9	Standard polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3239.4	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3192.6	Standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3649.0	Standard polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3435.8	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3229.2	Standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	4187.3	Standard polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3429.1	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3241.5	Standard non polar	33892256
LysoPE(14:0/0:0),3TMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3750.4	Standard polar	33892256
LysoPE(14:0/0:0),4TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3431.3	Semi standard non polar	33892256
LysoPE(14:0/0:0),4TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3235.7	Standard non polar	33892256
LysoPE(14:0/0:0),4TMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3507.0	Standard polar	33892256
LysoPE(14:0/0:0),1TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN)O[Si](C)(C)C(C)(C)C	3412.7	Semi standard non polar	33892256
LysoPE(14:0/0:0),1TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C	3369.7	Semi standard non polar	33892256
LysoPE(14:0/0:0),1TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C	3476.3	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3639.0	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3259.1	Standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4486.0	Standard polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3716.4	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3429.7	Standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4440.7	Standard polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3710.2	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3446.0	Standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4005.4	Standard polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3883.8	Semi standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3467.7	Standard non polar	33892256
LysoPE(14:0/0:0),2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4469.6	Standard polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3939.5	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3550.3	Standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3823.4	Standard polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4166.4	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3605.7	Standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4175.1	Standard polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4129.2	Semi standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3605.9	Standard non polar	33892256
LysoPE(14:0/0:0),3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3881.5	Standard polar	33892256
LysoPE(14:0/0:0),4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4380.8	Semi standard non polar	33892256
LysoPE(14:0/0:0),4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3692.0	Standard non polar	33892256
LysoPE(14:0/0:0),4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(OCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3742.7	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(14:0/0:0) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0f8c-2911000000-86ea0ed79b0f5580d992	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(14:0/0:0) GC-MS (1 TMS) - 70eV, Positive	splash10-0fal-9720200000-243977cbaca52f7a857c	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(14:0/0:0) GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPE(14:0/0:0) 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 - LysoPE(14:0/0:0) 10V, Positive-QTOF	splash10-0006-9120200000-9b9a6fa301a3fbb353cd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 20V, Positive-QTOF	splash10-0006-9220000000-199682174fa93ae85710	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 40V, Positive-QTOF	splash10-0006-9210000000-0926981af84bff71db6c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 10V, Negative-QTOF	splash10-05di-1292300000-0bafd14d254b9378e281	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 20V, Negative-QTOF	splash10-004i-6690000000-b66272ac38a083a70f16	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 40V, Negative-QTOF	splash10-01t9-9110000000-db6cee0f6bda0ce92bd8	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 10V, Positive-QTOF	splash10-004i-4021900000-942e80bfa8ac0c116b2c	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 20V, Positive-QTOF	splash10-000f-9131000000-77e107464990b9be3058	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 40V, Positive-QTOF	splash10-0006-9200000000-885446d5aebbc5fe1163	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 10V, Negative-QTOF	splash10-00di-0004900000-ae2b33ce090d5f699a34	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 20V, Negative-QTOF	splash10-004i-1391300000-0a37e1a6d8993b2d90f7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPE(14:0/0:0) 40V, Negative-QTOF	splash10-004i-1390000000-0de3894f8d18473b1768	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, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Feces

Tissue Locations

All Tissues

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Iron deficiency	26848182	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Ulcerative colitis	26848182	details

Associated Disorders and Diseases

Disease References

Iron deficiency
Lee T, Clavel T, Smirnov K, Schmidt A, Lagkouvardos I, Walker A, Lucio M, Michalke B, Schmitt-Kopplin P, Fedorak R, Haller D: Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD. Gut. 2017 May;66(5):863-871. doi: 10.1136/gutjnl-2015-309940. Epub 2016 Feb 4. [PubMed:26848182 ]
Ulcerative colitis
Lee T, Clavel T, Smirnov K, Schmidt A, Lagkouvardos I, Walker A, Lucio M, Michalke B, Schmitt-Kopplin P, Fedorak R, Haller D: Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD. Gut. 2017 May;66(5):863-871. doi: 10.1136/gutjnl-2015-309940. Epub 2016 Feb 4. [PubMed:26848182 ]

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB028216

KNApSAcK ID

Not Available

Chemspider ID

7826020

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9547070

PDB ID

Not Available

ChEBI ID

84299

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Divecha N, Irvine RF: Phospholipid signaling. Cell. 1995 Jan 27;80(2):269-78. [PubMed:7834746 ]
Cevc, Gregor (1993). Phospholipids Handbook. Marcel Dekker.
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. Ectonucleotide pyrophosphatase/phosphodiesterase family member 2

General function:: Involved in catalytic activity
Specific function:: Hydrolyzes lysophospholipids to produce lysophosphatidic acid (LPA) in extracellular fluids. Major substrate is lysophosphatidylcholine. Also can act on sphingosylphosphphorylcholine producing sphingosine-1-phosphate, a modulator of cell motility. Can hydrolyze, in vitro, bis-pNPP, to some extent pNP-TMP, and barely ATP. Involved in several motility-related processes such as angiogenesis and neurite outgrowth. Acts as an angiogenic factor by stimulating migration of smooth muscle cells and microtubule formation. Stimulates migration of melanoma cells, probably via a pertussis toxin-sensitive G protein. May have a role in induction of parturition. Possible involvement in cell proliferation and adipose tissue development. Tumor cell motility-stimulating factor.
Gene Name:: ENPP2
Uniprot ID:: Q13822
Molecular weight:: 98992.78

Showing metabocard for LysoPE(14:0/0:0) (HMDB0011500)

MOL for HMDB0011500 (LysoPE(14:0/0:0))

3D MOL for HMDB0011500 (LysoPE(14:0/0:0))

3D SDF for HMDB0011500 (LysoPE(14:0/0:0))

3D-SDF for HMDB0011500 (LysoPE(14:0/0:0))

PDB for HMDB0011500 (LysoPE(14:0/0:0))

3D PDB for HMDB0011500 (LysoPE(14:0/0:0))

SMILES for HMDB0011500 (LysoPE(14:0/0:0))

INCHI for HMDB0011500 (LysoPE(14:0/0:0))

Structure for HMDB0011500 (LysoPE(14:0/0:0))

3D Structure for HMDB0011500 (LysoPE(14:0/0:0))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes