| SpectraBase Compound ID | 6AkGyFvRS83 |
|---|---|
| InChI | InChI=1S/C75H128O17P2/c1-5-9-13-17-21-25-29-31-32-33-34-35-36-38-41-44-48-52-56-60-73(78)86-66-71(92-75(80)62-58-54-50-46-42-37-30-26-22-18-14-10-6-2)68-90-94(83,84)88-64-69(76)63-87-93(81,82)89-67-70(91-74(79)61-57-53-49-45-40-28-24-20-16-12-8-4)65-85-72(77)59-55-51-47-43-39-27-23-19-15-11-7-3/h9,13,19-21,23-26,30-32,34-35,38,41,48,52,69-71,76H,5-8,10-12,14-18,22,27-29,33,36-37,39-40,42-47,49-51,53-68H2,1-4H3,(H,81,82)(H,83,84)/b13-9-,23-19-,24-20-,25-21-,30-26-,32-31-,35-34-,41-38-,52-48- |
| InChIKey | LFSZGRORNLIVJI-GMQOIZAINA-N |
| Mol Weight | 1363.8 g/mol |
| Molecular Formula | C75H128O17P2 |
| Exact Mass | 1362.862677 g/mol |
| SpectraBase Spectrum ID | 9rs9Z7DOvsZ |
|---|---|
| Name | CL 14:1_14:1_16:1_22:6 |
| Classification | Glycerophospholipids [GP] |
| Comments | Cardiolipin |
| Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
| Exact Mass | 1362.862676641 u |
| Formula | C75H128O17P2 |
| InChI | InChI=1S/C75H128O17P2/c1-5-9-13-17-21-25-29-31-32-33-34-35-36-38-41-44-48-52-56-60-73(78)86-66-71(92-75(80)62-58-54-50-46-42-37-30-26-22-18-14-10-6-2)68-90-94(83,84)88-64-69(76)63-87-93(81,82)89-67-70(91-74(79)61-57-53-49-45-40-28-24-20-16-12-8-4)65-85-72(77)59-55-51-47-43-39-27-23-19-15-11-7-3/h9,13,19-21,23-26,30-32,34-35,38,41,48,52,69-71,76H,5-8,10-12,14-18,22,27-29,33,36-37,39-40,42-47,49-51,53-68H2,1-4H3,(H,81,82)(H,83,84)/b13-9-,23-19-,24-20-,25-21-,30-26-,32-31-,35-34-,41-38-,52-48- |
| InChIKey | LFSZGRORNLIVJI-GMQOIZAINA-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 | CCCCCC\C=C/CCCCCCCC(=O)OC(COC(=O)CC\C=C/C\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)CCCCCCC\C=C/CCCC)OC(=O)CCCCCCC\C=C/CCCC |
| Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |