The LIPID MAPS consortium has developed a comprehensive classification, nomenclature, and chemical representation system for lipids. The details of the classification system first appeared in the May 2005 issue of the Journal of Lipid Research: Fahy, E. et al A comprehensive classification system for lipids, J. Lipid Res.(2005) 46, 839-861. PubMed ID: 15722563. Since then, a substantial number of updates and improvements have been made to the classification system, some of which are described in the following papers: Fahy E. et al Update of the LIPID MAPS comprehensive classification system for lipids. J. Lipid Res.. (2009) 50: p. S9-S14.PubMed ID:19098281. Liebisch G. et al Update on LIPID MAPS classification, nomenclature, and shorthand notation for MS-derived lipid structures J. Lipid Res.. (2020) 61: p1539-1555.PubMed ID:33037133. and these are outlined below:
Instead of drawing all possible structural isomers explicitly for Diradylglycerols and Triradylglycerols, the LIPID MAPS abbreviation scheme supports the isomeric specification. A suffix containing 'iso' along with the number of possible isomers is appended to the abbreviation (e.g. [iso2],[iso6]) and a single unique LM_ID is assigned. The structure assigned to the LM_ID corresponds to the radyl substitution shown in the abbreviation. An option is provided to display the other isomers in the group.
The [rac] designation refers to racemic mixtures due to substitution at the sn1 and sn3 positions of glycerol.
Examples: Abbreviation: DG(16:0/16:1(9Z)/0:0)[iso2]; LM_ID: LMGL02010010; Systematic name: 1-hexadecanoyl-2-(9Z-hexadecenoyl)-sn-glycerol Abbreviation: TG(16:1(9Z)/17:0/17:0)[iso3]; LM_ID: LMGL03010027; Systematic name: 1-(9Z-hexadecenoyl)-2,3-diheptadecanoyl-sn-glycerol Abbreviation: TG(16:0/17:0/17:1(9Z))[iso6]; LM_ID: LMGL03010028; Systematic name: 1-hexadecanoyl-2-heptadecanoyl-3-(9Z-heptadecenoyl)-sn-glycerol.
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 C2 carbon of the glycerol group, the stereochemistry specification of [U] is appended to the abbreviation and the structure is drawn with C2 stereochemistry unspecified. For example: Abbreviation - PC(16:0/18:1(9E)[U]); LMID - LMGP01010582; Systematic name - 1-hexadecanoyl-2-(9E-octadecenoyl)-sn-glycero-3-phosphocholine.
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