Structure database (LMSD)

  MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".
LM IDLMGP03020023
Common NamePS(O-18:0/15:1(9Z))
Systematic Name1-octadecyl-2-(9Z-pentadecenoyl)-glycero-3-phosphoserine
SynonymsPS(O-33:1); PS(O-18:0/15:1)
Exact Mass
733.5258 (neutral)    Calculate m/z:
FormulaC39H76NO9P
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphoserines [GP03]
Sub Class1-alkyl,2-acylglycerophosphoserines [GP0302]
PubChem CID52926112
InChIKeyCWWOGJUZNOPGFM-FXFPHHKCSA-N  Show lipids differing only in stereochemistry/bond geometry
InChIInChI=1S/C39H76NO9P/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-46-33-36(3
4-47-50(44,45)48-35-37(40)39(42)43)49-38(41)31-29-27-25-23-21-16-14-12-10-8-6-4-
2/h12,14,36-37H,3-11,13,15-35,40H2,1-2H3,(H,42,43)(H,44,45)/b14-12-/t36-,37+/m1/
s1
SMILESC(O)(=O)[C@@]([H])(N)COP(OC[C@]([H])(OC(CCCCCCC/C=C\CCCCC)=O)COCCCCCCCCCCCCCCCCC
C)(=O)O
StatusActive (generated by computational methods)
Calculated physicochemical properties (?):
 Heavy Atoms50Rings0Aromatic Rings0Rotatable Bonds40
 van der Waals
Molecular Volume
785.28Topological Polar
Surface Area
154.61Hydrogen
Bond Donors
3Hydrogen
Bond Acceptors
9
 logP12.47Molar
Refractivity
206.03    
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.