Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	18768
Common Name:	PG(18:1(9Z)/0:0)
Systematic Name:	1-(9Z-octadecenoyl)-sn-glycero-3-phospho-(1'-sn-glycerol)
RefMet Name:	PG 18:1(9Z)/0:0
Synonyms:	9-Octadecenoic acid, 3-[[(2,3-dihydroxypropoxy)hydroxyphosphinyl]oxy]-2-hydroxypropyl ester, [R-(Z)]-; PG(18:1/0:0) [PubChem Synonyms]
Exact Mass:	510.2958 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C24H47O9P
InChIKey:	FQQQKGAFQIIGLQ-SNZQZGEVSA-N
LIPID MAPS Category:	Glycerophospholipids [GP]
LIPID MAPS mainclass:	Glycerophosphoglycerols [GP04]
LIPID MAPS subclass:	Monoacylglycerophosphoglycerols [GP0405]
SMILES:	CCCCCCCC/C=CCCCCCCCC(=O)OC[C@H](COP(=O)(O)OC[C@H](CO)O)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	9547135
LIPID MAPS ID:	LMGP04050006
CHEBI ID:	72952
HMDB ID:	HMDB0240602
Plant Metabolite Hub(Pmhub):	MS000239645

Calculated physicochemical properties (?):

Heavy Atoms:	34
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	25
van der Waals Molecular volume:	517.42 Å3 molecule-1
Toplogical Polar Sufrace Area:	142.75 Å2 molecule-1
Hydrogen Bond Donors:	4
Hydrogen Bond Acceptors:	9
logP:	6.30
Molar Refractivity:	134.09
Fraction sp3 Carbons:	0.88
sp3 Carbons:	21

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y