Structure database (LMSD)

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LM IDLMGP04020004
Common NamePG(O-16:0/14:1(9Z))
Systematic Name1-hexadecyl-2-(9Z-tetradecenoyl)-glycero-3-phospho-(1'-sn-glycerol)
SynonymsPG(O-30:1); PG(O-16:0/14:1)
Exact Mass
678.4836 (neutral)    Calculate m/z:
FormulaC36H71O9P
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphoglycerols [GP04]
Sub Class1-alkyl,2-acylglycerophosphoglycerols [GP0402]
PubChem CID52927252
SWISSLIPIDS IDSLM:000501611
InChIKeyUUORSEAQBARVDN-GQEPBNBKSA-N  Show lipids differing only in stereochemistry/bond geometry
InChIInChI=1S/C36H71O9P/c1-3-5-7-9-11-13-15-16-17-19-21-23-25-27-29-42-32-35(33-44-46
(40,41)43-31-34(38)30-37)45-36(39)28-26-24-22-20-18-14-12-10-8-6-4-2/h10,12,34-3
5,37-38H,3-9,11,13-33H2,1-2H3,(H,40,41)/b12-10-/t34-,35+/m0/s1
SMILES[C@]([H])(OC(CCCCCCC/C=C\CCCC)=O)(COP(=O)(O)OC[C@@]([H])(O)CO)COCCCCCCCCCCCCCCCC
StatusActive (generated by computational methods)
Calculated physicochemical properties (?):
 Heavy Atoms46Rings0Aromatic Rings0Rotatable Bonds37
 van der Waals
Molecular Volume
725.02Topological Polar
Surface Area
131.75Hydrogen
Bond Donors
3Hydrogen
Bond Acceptors
9
 logP11.53Molar
Refractivity
190.15    
LIPID MAPS abbreviations for glycerophospholipids (GP)

The LIPID MAPS glycerophospholipid abbreviations (PC, PE, etc.) are used here to refer to species with one or two radyl side-chains where the structures of the side chains are indicated within parentheses in the 'Headgroup(sn1/sn2)' format (e.g. PC(16:0/18:1(9Z)). By default, R stereochemistry at the C-2 carbon of glycerol and attachment of the headgroup at the sn3 position is assumed. Also, acyl chains are assumed by default. The 'O-' prefix is used to indicate the presence of an alkyl ether substituent e.g. PC(O-16:0/18:1(9Z)), whereas the 'P-' prefix is used for the 1Z-alkenyl ether (Plasmalogen) substituent e.g. PC(P-16:0/18:1(9Z)).

For molecules with opposite (S) stereochemistry at C2 of the glycerol group and attachment of the headgroup at the sn1 position, the stereochemistry specification of [S] is appended to the abbreviation. The 'Headgroup(sn3/sn2)' abbreviation format is used.

For molecules with unknown stereochemistry at the C-2 carbon of the glycerol group, the stereochemistry specification of [U] is appended to the abbreviation and the structure is drawn with C-2 stereochemistry unspecified.