Structure database (LMSD)Return to Databases Overview
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| LM ID | LMGP00000060 | |||||||||||||||||||||||||||
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| Common Name | PE(16:0/18:1(9Z))-15-isoLG lactam | |||||||||||||||||||||||||||
| Systematic Name | - | |||||||||||||||||||||||||||
| Synonyms | PE(34:1)-isoK lactam | |||||||||||||||||||||||||||
| Exact Mass | ||||||||||||||||||||||||||||
| Formula | C59H104NO12P | |||||||||||||||||||||||||||
| Category | Glycerophospholipids [GP] | |||||||||||||||||||||||||||
| Main Class | Other Glycerophospholipids [GP00] | |||||||||||||||||||||||||||
| Sub Class | - | |||||||||||||||||||||||||||
| PubChem CID | 52922111 | |||||||||||||||||||||||||||
| InChIKey | VVYVGBXNIXUCDE-ORZYWFCSSA-N Show lipids differing only in stereochemistry/bond geometry | |||||||||||||||||||||||||||
| InChI |
InChI=1S/C59H104NO12P/c1-5-8-11-13-15-17-19-21-22-24-26-28-30-32-39-44-58(65)72-53(49-69-57(64)43-38-31-29-27-25-23-20-18-16-14-12-9-6-2)50-71-73(67,68)70-48-47-60-51(4)54(41-36-33-34-37-42-56(62)63)55(59(60)66)46-45-52(61)40-35-10-7-3/h21-22,33,36,45-46,52-53,55,61H,5-20,23-32,34-35,37-44,47-50H2,1-4H3,(H,62,63)(H,67,68)/b22-21-,36-33-,46-45+/t52?,53-,55?/m1/s1
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| SMILES |
[C@](COP(=O)(O)OCCN1C(=O)C(/C=C/C(O)CCCCC)C(=C1C)C/C=C\CCCC(O)=O)([H])(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O
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| Status | Active | |||||||||||||||||||||||||||
| References | Isoketals form cytotoxic phosphatidylethanolamine adducts in cells C. Blake Sullivan, Elena Matafonova, L. Jackson Roberts II, Venkataraman Amarnath and Sean S. Davies J. Lipid Res. 2010 51:(5) 999-1009 | |||||||||||||||||||||||||||
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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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