Structure database (LMSD)

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LM IDLMGP05010002
Common NamePGP(16:0/18:1(11Z))
Systematic Name1-hexadecanoyl-2-(11Z-octadecenoyl)-sn-glycero-3-phospho-(1'-sn-glycerol-3'-
phosphate)
SynonymsPGP(16:0/18:1); PGP(34:1); PGP(16:0_18:1)
Exact Mass
828.4918 (neutral)    Calculate m/z:
FormulaC40H78O13P2
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphoglycerophosphates [GP05]
Sub ClassDiacylglycerophosphoglycerophosphates [GP0501]
AbbrevPGP 34:1
Abbrev ChainsPGP 16:0_18:1
PubChem CID9547136
HMDB IDHMDB0013475
SWISSLIPIDS IDSLM:000470887
InChIKeyBMNRKKFJIDDAOJ-GPJPVTGXSA-N  Show lipids differing only in stereochemistry/bond geometry
InChI
InChI=1S/C40H78O13P2/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-40(43)53-38(36-52-55(47,48)51-34-37(41)33-50-54(44,45)46)35-49-39(42)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h13,15,37-38,41H,3-12,14,16-36H2,1-2H3,(H,47,48)(H2,44,45,46)/b15-13-/t37-,38+/m0/s1
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SMILES
[C@]([H])(OC(CCCCCCCCC/C=C\CCCCCC)=O)(COP(=O)(O)OC[C@@]([H])(O)COP(=O)(O)O)COC(CCCCCCCCCCCCCCC)=O
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StatusActive
Calculated physicochemical properties (?):
 Heavy Atoms55Rings0Aromatic Rings0Rotatable Bonds43
 van der Waals
Molecular Volume
846.57Topological Polar
Surface Area
195.35Hydrogen
Bond Donors
4Hydrogen
Bond Acceptors
13
 logP12.79Molar
Refractivity
218.91    
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.