Structure database (LMSD)
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  MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".
LM IDLMGP10050006
Common NamePA(16:0/0:0)
Systematic Name1-hexadecanoyl-sn-glycero-3-phosphate
SynonymsHexadecanoic acid, 2-hydroxy-3-(phosphonooxy)propyl ester, (R)-; Palmitin, 1-
mono-, 3-(dihydrogen phosphate), L-; 1-Palmitoyl-sn-glycerol 3-phosphate; 1-
Palmitoyl-sn-glyceryl 3-phosphate; LPA(16:0); LPA(16:0)
Exact Mass
410.2433 (neutral)    Calculate m/z:
FormulaC19H39O7P
CategoryGlycerophospholipids [GP]
Main ClassGlycerophosphates [GP10]
Sub ClassMonoacylglycerophosphates [GP1005]
AbbrevLPA 16:0
Abbrev ChainsLPA 16:0
LIPIDAT ID7281
PubChem CID6419701
HMDB IDHMDB07853
CHEBI ID15799
SWISSLIPIDS IDSLM:000000421
CAYMAN ID10010094
InChIKeyYNDYKPRNFWPPFU-GOSISDBHSA-N  Show lipids differing only in stereochemistry/bond geometry
InChI
InChI=1S/C19H39O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(21)25-16-18(20)17-26-27(22,23)24/h18,20H,2-17H2,1H3,(H2,22,23,24)/t18-/m1/s1
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SMILES
[C@](COP(=O)(O)O)([H])(O)COC(CCCCCCCCCCCCCCC)=O
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MS SpectraView MoNA MS spectra      Predict MS/MS spectrum (Neg. mode)
StatusActive
Calculated physicochemical properties (?):
 Heavy Atoms27Rings0Aromatic Rings0Rotatable Bonds20
 van der Waals
Molecular Volume		415.98Topological Polar
Surface Area		113.29Hydrogen
Bond Donors		3Hydrogen
Bond Acceptors		7
 logP5.68Molar
Refractivity		106.49    
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.