SpectraBase Compound ID | Jev6hKEC6yq |
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InChI | InChI=1S/C77H130O17P2/c1-5-9-13-17-21-25-29-32-34-35-37-40-43-46-50-54-58-62-75(80)88-68-73(94-77(82)64-60-56-52-48-44-38-31-27-23-19-15-11-7-3)70-92-96(85,86)90-66-71(78)65-89-95(83,84)91-69-72(93-76(81)63-59-55-51-47-41-28-24-20-16-12-8-4)67-87-74(79)61-57-53-49-45-42-39-36-33-30-26-22-18-14-10-6-2/h9-10,13-14,20-22,24-26,32-34,36-37,40,42,45-46,50,71-73,78H,5-8,11-12,15-19,23,27-31,35,38-39,41,43-44,47-49,51-70H2,1-4H3,(H,83,84)(H,85,86)/b13-9-,14-10-,24-20-,25-21-,26-22-,34-32-,36-33-,40-37-,45-42-,50-46- |
InChIKey | IGMLXCFUTBCWNT-SGSCSFNRNA-N |
Mol Weight | 1389.8 g/mol |
Molecular Formula | C77H130O17P2 |
Exact Mass | 1388.878327 g/mol |
SpectraBase Spectrum ID | JFEwiPMsUb5 |
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Name | CL 14:1_18:4_16:0_20:5 |
Classification | Glycerophospholipids [GP] |
Comments | Cardiolipin |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1388.878326705 u |
Formula | C77H130O17P2 |
InChI | InChI=1S/C77H130O17P2/c1-5-9-13-17-21-25-29-32-34-35-37-40-43-46-50-54-58-62-75(80)88-68-73(94-77(82)64-60-56-52-48-44-38-31-27-23-19-15-11-7-3)70-92-96(85,86)90-66-71(78)65-89-95(83,84)91-69-72(93-76(81)63-59-55-51-47-41-28-24-20-16-12-8-4)67-87-74(79)61-57-53-49-45-42-39-36-33-30-26-22-18-14-10-6-2/h9-10,13-14,20-22,24-26,32-34,36-37,40,42,45-46,50,71-73,78H,5-8,11-12,15-19,23,27-31,35,38-39,41,43-44,47-49,51-70H2,1-4H3,(H,83,84)(H,85,86)/b13-9-,14-10-,24-20-,25-21-,26-22-,34-32-,36-33-,40-37-,45-42-,50-46- |
InChIKey | IGMLXCFUTBCWNT-SGSCSFNRNA-N |
Ion Polarity | N |
Literature Reference | Tsugawa, H.; Ikeda, K.; Takahashi, M.; Satoh, A.; Mori, Y.; Uchino, H.; Okahashi, N.; Yamada, Y.; Tada, I.; Bonini, P.; Higashi, Y.; Okazaki, Y.; Zhou, Z.; Zhu, Z.-J.; Koelmel, J.; Cajka, T.; Fiehn, O.; Saito, K.; Arita, M.; Arita, M. A Lipidome Atlas in MS-DIAL 4. Nature Biotechnology 2020, 38 (10), 1159–1163. |
Literature Reference DOI | https://doi.org/10.1038/s41587-020-0531-2 |
Precursor Ion | [M-H]- |
SMILES | CCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)COP(O)(=O)OCC(O)COP(O)(=O)OCC(COC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCC\C=C/CCCC |
Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |