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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2017-09-09 02:35:19 UTC

Update Date

2022-11-30 19:25:53 UTC

HMDB ID

HMDB0114744

Secondary Accession Numbers

None

Metabolite Identification

Common Name

LysoPA(18:3(9Z,12Z,15Z)/0:0)

Description

LysoPA(18:3(9Z,12Z,15Z)/0:0) is a lysophosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. Lysophosphatidic acids can have different combinations of fatty acids of varying lengths and saturation attached at the C-1 (sn-1) or C-2 (sn-2) position. Fatty acids containing 16 and 18 carbons are the most common. LysoPA(18:3(9Z,12Z,15Z)/0:0), in particular, consists of one chain of alpha-linolenic acid at the C-1 position. Lysophosphatidic acid is the simplest possible glycerophospholipid. It is the biosynthetic precursor of phosphatidic acid. Although it is present at very low levels only in animal tissues, it is extremely important biologically, influencing many biochemical processes.

Structure

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

LPA(18:3(9Z,12Z,15Z)/0:0)
  Mrv1652303302022372D          

 29 28  0  0  1  0            999 V2000
    9.1943   -4.4806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0108   -3.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0277   -5.2971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8442   -4.4637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0193   -4.4722    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    8.3810   -4.0225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6710   -4.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9522   -4.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2421   -4.4579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6798   -5.2676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5233   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5233   -3.2816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8092   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0951   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3810   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6669   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2386   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0146   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7287   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2678   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9819   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6960   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5210   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2351   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9493   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  5  1  1  0  0  0  0
  5  2  1  0  0  0  0
  5  3  2  0  0  0  0
  5  4  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

HMDB0114744
     RDKit          3D
LysoPA(18:3(9Z,12Z,15Z)/0:0)
 66 65  0  0  0  0  0  0  0  0999 V2000
    3.6314   -1.4870    2.6787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1492   -1.6735    2.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4732   -2.1399    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2550   -1.4476    0.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9050   -0.1607    0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    0.8896   -0.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    1.9677    0.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4560    2.3602    1.5123 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0776    2.5694    1.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    2.4175    1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9285    1.9783   -0.1830 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3286    3.0227   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9409    3.4276   -0.7536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0642    2.3161   -0.7655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1938    1.6488   -2.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2135    0.5489   -2.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5816    0.9934   -1.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4860   -0.1952   -1.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0366   -1.3258   -1.8641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7944   -0.0622   -1.2603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7823   -1.0393   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5534   -2.0823   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3898   -2.7936   -0.3162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7351   -3.0607   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8772   -2.3162    0.0998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2333   -3.3515    0.0967 P   0  0  0  0  0  5  0  0  0  0  0  0
   -9.0034   -4.3634   -0.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2879   -4.1400    1.5983 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5856   -2.4039   -0.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -0.7661    3.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2114   -1.0675    1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1386   -2.4662    2.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4328   -2.5071    3.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5883   -0.7196    2.8352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0551   -3.0993    0.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4613   -1.8441   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9258    0.1467    1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0130   -0.3061    0.4130 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6595    0.7392   -1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703    2.6841   -0.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598    1.6002    2.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1017    3.2731    1.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8901    2.9211    2.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0166    2.6524    1.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0494    1.1899   -0.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7044    1.3854   -0.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2872    2.5713   -2.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9751    3.9171   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6158    4.1645   -1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8614    3.9358    0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0818    1.5983    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0619    2.8188   -0.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5272    2.4073   -2.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651    1.1784   -2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -0.0099   -2.9774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -0.1824   -1.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5333    1.4292   -0.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0202    1.7088   -2.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7693   -0.5175   -0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9283   -1.5373   -2.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5715   -1.6356    0.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411   -2.7693    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5257   -3.7729    0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7138   -3.5823   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6814   -3.5800    2.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9610   -2.0558    0.6700 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 21 59  1  0
 21 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 28 65  1  0
 29 66  1  0
M  END

LPA(18:3(9Z,12Z,15Z)/0:0)
  Mrv1652303302022372D          

 29 28  0  0  1  0            999 V2000
    9.1943   -4.4806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0108   -3.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0277   -5.2971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8442   -4.4637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0193   -4.4722    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    8.3810   -4.0225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6710   -4.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9522   -4.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2421   -4.4579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6798   -5.2676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5233   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5233   -3.2816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8092   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0951   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3810   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6669   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2386   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0146   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7287   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2678   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9819   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6960   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5210   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2351   -4.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9493   -4.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  5  1  1  0  0  0  0
  5  2  1  0  0  0  0
  5  3  2  0  0  0  0
  5  4  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0114744

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H37O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(23)27-18-20(22)19-28-29(24,25)26/h3-4,6-7,9-10,20,22H,2,5,8,11-19H2,1H3,(H2,24,25,26)/b4-3-,7-6-,10-9-

> <INCHI_KEY>
DVNZKWQUAXJYGB-PDBXOOCHSA-N

> <FORMULA>
C21H37O7P

> <MOLECULAR_WEIGHT>
432.494

> <EXACT_MASS>
432.227690529

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.279392762817835

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{2-hydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy}phosphonic acid

> <ALOGPS_LOGP>
4.32

> <JCHEM_LOGP>
4.761846208333333

> <ALOGPS_LOGS>
-5.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.531115837556447

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.505317785248875

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4039997949880556

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
117.5322

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0114744
     RDKit          3D
LysoPA(18:3(9Z,12Z,15Z)/0:0)
 66 65  0  0  0  0  0  0  0  0999 V2000
    3.6314   -1.4870    2.6787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1492   -1.6735    2.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4732   -2.1399    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2550   -1.4476    0.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9050   -0.1607    0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    0.8896   -0.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    1.9677    0.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4560    2.3602    1.5123 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0776    2.5694    1.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    2.4175    1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9285    1.9783   -0.1830 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3286    3.0227   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9409    3.4276   -0.7536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0642    2.3161   -0.7655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1938    1.6488   -2.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2135    0.5489   -2.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5816    0.9934   -1.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4860   -0.1952   -1.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0366   -1.3258   -1.8641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7944   -0.0622   -1.2603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7823   -1.0393   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5534   -2.0823   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3898   -2.7936   -0.3162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7351   -3.0607   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8772   -2.3162    0.0998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2333   -3.3515    0.0967 P   0  0  0  0  0  5  0  0  0  0  0  0
   -9.0034   -4.3634   -0.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2879   -4.1400    1.5983 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5856   -2.4039   -0.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -0.7661    3.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2114   -1.0675    1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1386   -2.4662    2.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4328   -2.5071    3.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5883   -0.7196    2.8352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0551   -3.0993    0.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4613   -1.8441   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9258    0.1467    1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0130   -0.3061    0.4130 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6595    0.7392   -1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703    2.6841   -0.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598    1.6002    2.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1017    3.2731    1.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8901    2.9211    2.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0166    2.6524    1.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0494    1.1899   -0.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7044    1.3854   -0.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2872    2.5713   -2.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9751    3.9171   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6158    4.1645   -1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8614    3.9358    0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0818    1.5983    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0619    2.8188   -0.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5272    2.4073   -2.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651    1.1784   -2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -0.0099   -2.9774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -0.1824   -1.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5333    1.4292   -0.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0202    1.7088   -2.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7693   -0.5175   -0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9283   -1.5373   -2.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5715   -1.6356    0.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411   -2.7693    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5257   -3.7729    0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7138   -3.5823   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6814   -3.5800    2.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9610   -2.0558    0.6700 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 21 59  1  0
 21 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 28 65  1  0
 29 66  1  0
M  END

HEADER    PROTEIN                                 30-MAR-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: LPA(18:3(9Z,12Z,15Z)/0:0)                         
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-MAR-20         0                                  
HETATM    1  O   UNK     0      17.163  -8.364   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      18.687  -6.808   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      18.718  -9.888   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      20.243  -8.332   0.000  0.00  0.00           O+0
HETATM    5  P   UNK     0      18.703  -8.348   0.000  0.00  0.00           P+0
HETATM    6  C   UNK     0      15.645  -7.509   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.319  -8.293   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.977  -7.537   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      11.652  -8.321   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      14.336  -9.833   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.310  -7.566   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.310  -6.126   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.977  -8.337   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.644  -7.566   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.311  -8.337   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.978  -7.566   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.645  -8.337   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.312  -7.566   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.979  -8.337   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.354  -7.566   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.894  -7.566   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.227  -8.337   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.560  -7.566   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.100  -7.566   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -7.433  -8.337   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.766  -7.566   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -10.306  -7.566   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -11.639  -8.337   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -12.972  -7.566   0.000  0.00  0.00           C+0
CONECT    1    6    5                                                       
CONECT    2    5                                                            
CONECT    3    5                                                            
CONECT    4    5                                                            
CONECT    5    1    2    3    4                                             
CONECT    6    1    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8   11                                                       
CONECT   10    7                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   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   29                                                       
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   56    0
END

COMPND    HMDB0114744
HETATM    1  C1  UNL     1       3.631  -1.487   2.679  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.149  -1.674   2.540  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.473  -2.140   1.183  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.255  -1.448   0.393  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.905  -0.161   0.709  1.00  0.00           C  
HETATM    6  C6  UNL     1       6.452   0.890  -0.243  1.00  0.00           C  
HETATM    7  C7  UNL     1       5.824   1.968   0.174  1.00  0.00           C  
HETATM    8  C8  UNL     1       5.456   2.360   1.512  1.00  0.00           C  
HETATM    9  C9  UNL     1       4.078   2.569   1.900  1.00  0.00           C  
HETATM   10  C10 UNL     1       3.004   2.417   1.204  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.929   1.978  -0.183  1.00  0.00           C  
HETATM   12  C12 UNL     1       2.329   3.023  -1.109  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.941   3.428  -0.754  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.064   2.316  -0.766  1.00  0.00           C  
HETATM   15  C15 UNL     1      -0.194   1.649  -2.102  1.00  0.00           C  
HETATM   16  C16 UNL     1      -1.213   0.549  -2.019  1.00  0.00           C  
HETATM   17  C17 UNL     1      -2.582   0.993  -1.628  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.486  -0.195  -1.590  1.00  0.00           C  
HETATM   19  O1  UNL     1      -3.037  -1.326  -1.864  1.00  0.00           O  
HETATM   20  O2  UNL     1      -4.794  -0.062  -1.260  1.00  0.00           O  
HETATM   21  C19 UNL     1      -5.782  -1.039  -1.164  1.00  0.00           C  
HETATM   22  C20 UNL     1      -5.553  -2.082  -0.103  1.00  0.00           C  
HETATM   23  O3  UNL     1      -4.390  -2.794  -0.316  1.00  0.00           O  
HETATM   24  C21 UNL     1      -6.735  -3.061  -0.115  1.00  0.00           C  
HETATM   25  O4  UNL     1      -7.877  -2.316   0.100  1.00  0.00           O  
HETATM   26  P1  UNL     1      -9.233  -3.351   0.097  1.00  0.00           P  
HETATM   27  O5  UNL     1      -9.003  -4.363  -0.990  1.00  0.00           O  
HETATM   28  O6  UNL     1      -9.288  -4.140   1.598  1.00  0.00           O  
HETATM   29  O7  UNL     1     -10.586  -2.404  -0.172  1.00  0.00           O  
HETATM   30  H1  UNL     1       3.426  -0.766   3.479  1.00  0.00           H  
HETATM   31  H2  UNL     1       3.211  -1.068   1.730  1.00  0.00           H  
HETATM   32  H3  UNL     1       3.139  -2.466   2.815  1.00  0.00           H  
HETATM   33  H4  UNL     1       5.433  -2.507   3.243  1.00  0.00           H  
HETATM   34  H5  UNL     1       5.588  -0.720   2.835  1.00  0.00           H  
HETATM   35  H6  UNL     1       5.055  -3.099   0.802  1.00  0.00           H  
HETATM   36  H7  UNL     1       6.461  -1.844  -0.609  1.00  0.00           H  
HETATM   37  H8  UNL     1       6.926   0.147   1.733  1.00  0.00           H  
HETATM   38  H9  UNL     1       8.013  -0.306   0.413  1.00  0.00           H  
HETATM   39  H10 UNL     1       6.660   0.739  -1.330  1.00  0.00           H  
HETATM   40  H11 UNL     1       5.570   2.684  -0.639  1.00  0.00           H  
HETATM   41  H12 UNL     1       5.860   1.600   2.272  1.00  0.00           H  
HETATM   42  H13 UNL     1       6.102   3.273   1.850  1.00  0.00           H  
HETATM   43  H14 UNL     1       3.890   2.921   2.978  1.00  0.00           H  
HETATM   44  H15 UNL     1       2.017   2.652   1.734  1.00  0.00           H  
HETATM   45  H16 UNL     1       2.049   1.190  -0.154  1.00  0.00           H  
HETATM   46  H17 UNL     1       3.704   1.385  -0.616  1.00  0.00           H  
HETATM   47  H18 UNL     1       2.287   2.571  -2.136  1.00  0.00           H  
HETATM   48  H19 UNL     1       2.975   3.917  -1.213  1.00  0.00           H  
HETATM   49  H20 UNL     1       0.616   4.165  -1.528  1.00  0.00           H  
HETATM   50  H21 UNL     1       0.861   3.936   0.228  1.00  0.00           H  
HETATM   51  H22 UNL     1       0.082   1.598   0.044  1.00  0.00           H  
HETATM   52  H23 UNL     1      -1.062   2.819  -0.565  1.00  0.00           H  
HETATM   53  H24 UNL     1      -0.527   2.407  -2.855  1.00  0.00           H  
HETATM   54  H25 UNL     1       0.765   1.178  -2.407  1.00  0.00           H  
HETATM   55  H26 UNL     1      -1.303  -0.010  -2.977  1.00  0.00           H  
HETATM   56  H27 UNL     1      -0.860  -0.182  -1.259  1.00  0.00           H  
HETATM   57  H28 UNL     1      -2.533   1.429  -0.608  1.00  0.00           H  
HETATM   58  H29 UNL     1      -3.020   1.709  -2.324  1.00  0.00           H  
HETATM   59  H30 UNL     1      -6.769  -0.517  -0.988  1.00  0.00           H  
HETATM   60  H31 UNL     1      -5.928  -1.537  -2.165  1.00  0.00           H  
HETATM   61  H32 UNL     1      -5.571  -1.636   0.916  1.00  0.00           H  
HETATM   62  H33 UNL     1      -3.841  -2.769   0.511  1.00  0.00           H  
HETATM   63  H34 UNL     1      -6.526  -3.773   0.718  1.00  0.00           H  
HETATM   64  H35 UNL     1      -6.714  -3.582  -1.078  1.00  0.00           H  
HETATM   65  H36 UNL     1      -9.681  -3.580   2.288  1.00  0.00           H  
HETATM   66  H37 UNL     1     -10.961  -2.056   0.670  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3   33   34
CONECT    3    4    4   35
CONECT    4    5   36
CONECT    5    6   37   38
CONECT    6    7    7   39
CONECT    7    8   40
CONECT    8    9   41   42
CONECT    9   10   10   43
CONECT   10   11   44
CONECT   11   12   45   46
CONECT   12   13   47   48
CONECT   13   14   49   50
CONECT   14   15   51   52
CONECT   15   16   53   54
CONECT   16   17   55   56
CONECT   17   18   57   58
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   59   60
CONECT   22   23   24   61
CONECT   23   62
CONECT   24   25   63   64
CONECT   25   26
CONECT   26   27   27   28   29
CONECT   28   65
CONECT   29   66
END

HMDB0114744
     RDKit          3D
LysoPA(18:3(9Z,12Z,15Z)/0:0)
 66 65  0  0  0  0  0  0  0  0999 V2000
    3.6314   -1.4870    2.6787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1492   -1.6735    2.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4732   -2.1399    1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2550   -1.4476    0.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9050   -0.1607    0.7092 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    0.8896   -0.2428 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8237    1.9677    0.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4560    2.3602    1.5123 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0776    2.5694    1.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0036    2.4175    1.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9285    1.9783   -0.1830 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3286    3.0227   -1.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9409    3.4276   -0.7536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0642    2.3161   -0.7655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1938    1.6488   -2.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2135    0.5489   -2.0186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5816    0.9934   -1.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4860   -0.1952   -1.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0366   -1.3258   -1.8641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7944   -0.0622   -1.2603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7823   -1.0393   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5534   -2.0823   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3898   -2.7936   -0.3162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7351   -3.0607   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8772   -2.3162    0.0998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2333   -3.3515    0.0967 P   0  0  0  0  0  5  0  0  0  0  0  0
   -9.0034   -4.3634   -0.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2879   -4.1400    1.5983 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5856   -2.4039   -0.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -0.7661    3.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2114   -1.0675    1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1386   -2.4662    2.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4328   -2.5071    3.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5883   -0.7196    2.8352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0551   -3.0993    0.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4613   -1.8441   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9258    0.1467    1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0130   -0.3061    0.4130 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6595    0.7392   -1.3296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703    2.6841   -0.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8598    1.6002    2.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1017    3.2731    1.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8901    2.9211    2.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0166    2.6524    1.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0494    1.1899   -0.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7044    1.3854   -0.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2872    2.5713   -2.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9751    3.9171   -1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6158    4.1645   -1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8614    3.9358    0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0818    1.5983    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0619    2.8188   -0.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5272    2.4073   -2.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651    1.1784   -2.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -0.0099   -2.9774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -0.1824   -1.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5333    1.4292   -0.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0202    1.7088   -2.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7693   -0.5175   -0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9283   -1.5373   -2.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5715   -1.6356    0.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411   -2.7693    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5257   -3.7729    0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7138   -3.5823   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6814   -3.5800    2.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9610   -2.0558    0.6700 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 21 59  1  0
 21 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 24 64  1  0
 28 65  1  0
 29 66  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-alpha-Linolenoyl-glycero-3-phosphate	HMDB
1-alpha-Linolenoyl-lysophosphatidic acid	HMDB
LPA(18:3)	HMDB
LPA(18:3(9Z,12Z,15Z))	HMDB
LPA(18:3n3/0:0)	HMDB
LPA(18:3W3/0:0)	HMDB
LPA(18:3n3)	HMDB
LPA(18:3W3)	HMDB
Lysophosphatidic acid(18:3(9Z,12Z,15Z)/0:0)	HMDB
Lysophosphatidic acid(18:3)	HMDB
Lysophosphatidic acid(18:3(9Z,12Z,15Z))	HMDB
Lysophosphatidic acid(18:3n3/0:0)	HMDB
Lysophosphatidic acid(18:3W3/0:0)	HMDB
Lysophosphatidic acid(18:3n3)	HMDB
Lysophosphatidic acid(18:3W3)	HMDB
LPA(18:3(9Z,12Z,15Z)/0:0)	HMDB
LPA(18:3/0:0)	HMDB
1-(9Z,12Z,15Z-Octadeatrienoyl)-phosphatidic acid	HMDB
Lysophosphatidic acid(18:3/0:0)	HMDB
1-a-Linolenoyl-glycero-3-phosphate	HMDB
1-(9Z,12Z,15Z-Octadeatrienoyl)-glycero-3-phosphate	HMDB
1-alpha-linolenoyl-glycero-3-phosphate	SMPDB, HMDB
1-alpha-linolenoyl-lysophosphatidic acid	SMPDB, HMDB
LPA(18:3)	SMPDB, HMDB
LPA(18:3(9Z,12Z,15Z))	SMPDB, HMDB
LPA(18:3n3/0:0)	SMPDB, HMDB
LPA(18:3w3/0:0)	SMPDB, HMDB
LPA(18:3n3)	SMPDB, HMDB
LPA(18:3w3)	SMPDB, HMDB
Lysophosphatidic acid(18:3(9Z,12Z,15Z)/0:0)	SMPDB, HMDB
Lysophosphatidic acid(18:3)	SMPDB, HMDB
Lysophosphatidic acid(18:3(9Z,12Z,15Z))	SMPDB, HMDB
Lysophosphatidic acid(18:3n3/0:0)	SMPDB, HMDB
Lysophosphatidic acid(18:3w3/0:0)	SMPDB, HMDB
Lysophosphatidic acid(18:3n3)	SMPDB, HMDB

Chemical Formula

C₂₁H₃₇O₇P

Average Molecular Weight

432.494

Monoisotopic Molecular Weight

432.227690529

IUPAC Name

{2-hydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxy}phosphonic acid

Traditional Name

2-hydroxy-3-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]propoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O

InChI Identifier

InChI=1S/C21H37O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(23)27-18-20(22)19-28-29(24,25)26/h3-4,6-7,9-10,20,22H,2,5,8,11-19H2,1H3,(H2,24,25,26)/b4-3-,7-6-,10-9-

InChI Key

DVNZKWQUAXJYGB-PDBXOOCHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-1 position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphates

Direct Parent

1-acylglycerol-3-phosphates

Alternative Parents

Substituents

1-acylglycerol-3-phosphate
Fatty acid ester
Monoalkyl phosphate
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Not Available

Process

Naturally occurring process

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
logP	4.32	ALOGPS
logP	4.76	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	1.51	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	117.53 m³·mol⁻¹	ChemAxon
Polarizability	47.28 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]+	211.711	31661259
DarkChem	[M-H]-	207.811	31661259
DeepCCS	[M+H]+	198.281	30932474
DeepCCS	[M-H]-	195.813	30932474
DeepCCS	[M-2H]-	229.602	30932474
DeepCCS	[M+Na]+	205.069	30932474
AllCCS	[M+H]+	208.6	32859911
AllCCS	[M+H-H2O]+	206.6	32859911
AllCCS	[M+NH4]+	210.6	32859911
AllCCS	[M+Na]+	211.1	32859911
AllCCS	[M-H]-	203.9	32859911
AllCCS	[M+Na-2H]-	206.6	32859911
AllCCS	[M+HCOO]-	209.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
LysoPA(18:3(9Z,12Z,15Z)/0:0)	CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O	3914.9	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0)	CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O	2765.6	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0)	CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O	3233.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
LysoPA(18:3(9Z,12Z,15Z)/0:0),1TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O)O[Si](C)(C)C	3335.1	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),1TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O)O[Si](C)(C)C	3286.6	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3306.4	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3030.7	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	3816.1	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3249.0	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3041.3	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	3586.1	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3282.5	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3062.7	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	3303.4	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),1TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	3573.3	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),1TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	3490.7	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3733.6	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3336.8	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3846.5	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3688.6	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3304.4	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),2TBDMS,isomer #2	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3686.9	Standard polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3922.6	Semi standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3451.8	Standard non polar	33892256
LysoPA(18:3(9Z,12Z,15Z)/0:0),3TBDMS,isomer #1	CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OCC(COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3444.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) GC-MS (1 TMS) - 70eV, Positive	splash10-03ds-9440000000-bbdd6e79093026413d38	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/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 - LysoPA(18:3(9Z,12Z,15Z)/0:0) 10V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 20V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 40V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 10V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 20V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 40V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 10V, Negative-QTOF	splash10-001i-0000900000-6fe5a0721925d7402523	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 20V, Negative-QTOF	splash10-001i-0000900000-6fe5a0721925d7402523	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 40V, Negative-QTOF	splash10-0ugi-2950600000-3b4c6c0770f021a90a0d	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 10V, Positive-QTOF	splash10-001i-0000900000-108d02e82a2642c9aead	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 20V, Positive-QTOF	splash10-001i-0000900000-108d02e82a2642c9aead	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - LysoPA(18:3(9Z,12Z,15Z)/0:0) 40V, Positive-QTOF	splash10-02mi-0950700000-e34f2b7be7c16d75d15a	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
De Novo Triacylglycerol Biosynthesis TG(18:3(9Z,12Z,15Z)/14:0/18:3(9Z,12Z,15Z))		Not Available
De Novo Triacylglycerol Biosynthesis TG(18:3(9Z,12Z,15Z)/14:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))		Not Available
De Novo Triacylglycerol Biosynthesis TG(18:3(9Z,12Z,15Z)/16:0/18:3(9Z,12Z,15Z))		Not Available
De Novo Triacylglycerol Biosynthesis TG(18:3(9Z,12Z,15Z)/16:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z))		Not Available
De Novo Triacylglycerol Biosynthesis TG(18:3(9Z,12Z,15Z)/18:0/18:3(9Z,12Z,15Z))		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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

20833812

PDB ID

Not Available

ChEBI ID

Not Available

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

Moritz A, De Graan PN, Gispen WH, Wirtz KW: Phosphatidic acid is a specific activator of phosphatidylinositol-4-phosphate kinase. J Biol Chem. 1992 Apr 15;267(11):7207-10. [PubMed:1313792 ]
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 ]
Moolenaar WH, Kruijer W, Tilly BC, Verlaan I, Bierman AJ, de Laat SW: Growth factor-like action of phosphatidic acid. Nature. 1986 Sep 11-17;323(6084):171-3. [PubMed:3748188 ]
Yang CY, Frohman MA: Mitochondria: signaling with phosphatidic acid. Int J Biochem Cell Biol. 2012 Aug;44(8):1346-50. doi: 10.1016/j.biocel.2012.05.006. Epub 2012 May 15. [PubMed:22609101 ]
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.

Showing metabocard for LysoPA(18:3(9Z,12Z,15Z)/0:0) (HMDB0114744)

MOL for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

3D MOL for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

3D SDF for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

3D-SDF for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

PDB for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

3D PDB for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

SMILES for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

INCHI for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

Structure for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

3D Structure for HMDB0114744 (LysoPA(18:3(9Z,12Z,15Z)/0:0))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra