Structure database (LMSD)Return to Databases Overview
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| LM ID | LMGP01050091 | |||||||||||||||||||||||||||
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| Common Name | PC(0:0/5:0) | |||||||||||||||||||||||||||
| Systematic Name | 2-valeryl-sn-glycero-3-phosphocholine | |||||||||||||||||||||||||||
| Synonyms | LPC(5:0) | |||||||||||||||||||||||||||
| Exact Mass | ||||||||||||||||||||||||||||
| Formula | C13H28NO7P | |||||||||||||||||||||||||||
| Category | Glycerophospholipids [GP] | |||||||||||||||||||||||||||
| Main Class | Glycerophosphocholines [GP01] | |||||||||||||||||||||||||||
| Sub Class | Monoacylglycerophosphocholines [GP0105] | |||||||||||||||||||||||||||
| Abbrev | LPC 5:0 | |||||||||||||||||||||||||||
| Abbrev Chains | LPC 5:0 | |||||||||||||||||||||||||||
| LIPIDAT ID | 10564 | |||||||||||||||||||||||||||
| PubChem CID | 24779499 | |||||||||||||||||||||||||||
| InChIKey | FUNVSMBQMVEBQX-GFCCVEGCSA-N Show lipids differing only in stereochemistry/bond geometry | |||||||||||||||||||||||||||
| InChI |
InChI=1S/C13H28NO7P/c1-5-6-7-13(16)21-12(10-15)11-20-22(17,18)19-9-8-14(2,3)4/h12,15H,5-11H2,1-4H3/t12-/m1/s1
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| SMILES |
[C@](COP(=O)([O-])OCC[N+](C)(C)C)([H])(OC(CCCC)=O)CO
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| Status | Active | |||||||||||||||||||||||||||
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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. |
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