Structure database (LMSD)

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LM IDLMGP03010006
Common NamePS(17:0/14:1(9Z))
Systematic Name1-heptadecanoyl-2-(9Z-tetradecenoyl)-sn-glycero-3-phosphoserine
SynonymsPS(17:0/14:1); PS(31:1); PS(14:1_17:0)
Exact Mass
719.4737 (neutral)    Calculate m/z:
FormulaC37H70NO10P
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphoserines [GP03]
Sub ClassDiacylglycerophosphoserines [GP0301]
PubChem CID5283507
SWISSLIPIDS IDSLM:000007423
InChIKeyALGRKSHPONJILC-HLNMDXRWSA-N  Show lipids differing only in stereochemistry/bond geometry
InChI
InChI=1S/C37H70NO10P/c1-3-5-7-9-11-13-15-16-17-19-20-22-24-26-28-35(39)45-30-33(31-46-49(43,44)47-32-34(38)37(41)42)48-36(40)29-27-25-23-21-18-14-12-10-8-6-4-2/h10,12,33-34H,3-9,11,13-32,38H2,1-2H3,(H,41,42)(H,43,44)/b12-10-/t33-,34+/m1/s1
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SMILES
C(O)(=O)[C@@]([H])(N)COP(OC[C@]([H])(OC(CCCCCCC/C=C\CCCC)=O)COC(CCCCCCCCCCCCCCCC)=O)(=O)O
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MS SpectraView MoNA MS spectra      Predict MS/MS spectrum (Neg. mode)
MS StandardView lipid standard
StatusActive
Calculated physicochemical properties (?):
 Heavy Atoms49Rings0Aromatic Rings0Rotatable Bonds38
 van der Waals
Molecular Volume
756.83Topological Polar
Surface Area
171.68Hydrogen
Bond Donors
3Hydrogen
Bond Acceptors
10
 logP10.93Molar
Refractivity
196.45    
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.