Structure database (LMSD)

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LM IDLMGP06010425
Common NamePI(19:0/15:1(9Z))
Systematic Name1-nonadecanoyl-2-(9Z-pentadecenoyl)-glycero-3-phospho-(1'-myo-inositol)
SynonymsPI(34:1); PI(15:1_19:0)
Exact Mass
836.5415 (neutral)    Calculate m/z:
FormulaC43H81O13P
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphoinositols [GP06]
Sub ClassDiacylglycerophosphoinositols [GP0601]
AbbrevPI 34:1
Abbrev ChainsPI 15:1_19:0
PubChem CID52927878
InChIKeyMLHFAQNWNDSKNM-ZPPDQBLHSA-N  Show lipids differing only in stereochemistry/bond geometry
InChI
InChI=1S/C43H81O13P/c1-3-5-7-9-11-13-15-17-18-19-20-22-23-25-27-29-31-36(44)53-33-35(55-37(45)32-30-28-26-24-21-16-14-12-10-8-6-4-2)34-54-57(51,52)56-43-41(49)39(47)38(46)40(48)42(43)50/h12,14,35,38-43,46-50H,3-11,13,15-34H2,1-2H3,(H,51,52)/b14-12-/t35-,38-,39-,40+,41-,42-,43-/m1/s1
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SMILES
[C@]([H])(OC(CCCCCCC/C=C\CCCCC)=O)(COP(=O)(O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)COC(CCCCCCCCCCCCCCCCCC)=O
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MS SpectraView MoNA MS spectra      Predict MS/MS spectrum (Neg. mode)
StatusActive (generated by computational methods)
Calculated physicochemical properties (?):
 Heavy Atoms57Rings1Aromatic Rings0Rotatable Bonds39
 van der Waals
Molecular Volume
866.28Topological Polar
Surface Area
209.51Hydrogen
Bond Donors
6Hydrogen
Bond Acceptors
13
 logP11.03Molar
Refractivity
225.71    
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.