SpectraBase Compound ID | CfIaTCKnI9g |
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InChI | InChI=1S/C75H124O17P2/c1-5-9-13-17-21-25-29-31-33-34-36-37-41-44-48-52-56-60-73(78)86-66-71(92-75(80)62-58-54-50-46-42-38-35-32-30-26-22-18-14-10-6-2)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/h9-10,13-14,19-26,31-33,35-37,42,44,46,48,69-71,76H,5-8,11-12,15-18,27-30,34,38-41,43,45,47,49-68H2,1-4H3,(H,81,82)(H,83,84)/b13-9-,14-10-,23-19-,24-20-,25-21-,26-22-,33-31-,35-32-,37-36-,46-42-,48-44- |
InChIKey | PQYYGKKQLURZNL-MEHBGYSTNA-N |
Mol Weight | 1359.7 g/mol |
Molecular Formula | C75H124O17P2 |
Exact Mass | 1358.831377 g/mol |
SpectraBase Spectrum ID | 2jShTXNoBKf |
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Name | CL 14:1_14:1_18:4_20:5 |
Classification | Glycerophospholipids [GP] |
Comments | Cardiolipin |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1358.831376512 u |
Formula | C75H124O17P2 |
InChI | InChI=1S/C75H124O17P2/c1-5-9-13-17-21-25-29-31-33-34-36-37-41-44-48-52-56-60-73(78)86-66-71(92-75(80)62-58-54-50-46-42-38-35-32-30-26-22-18-14-10-6-2)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/h9-10,13-14,19-26,31-33,35-37,42,44,46,48,69-71,76H,5-8,11-12,15-18,27-30,34,38-41,43,45,47,49-68H2,1-4H3,(H,81,82)(H,83,84)/b13-9-,14-10-,23-19-,24-20-,25-21-,26-22-,33-31-,35-32-,37-36-,46-42-,48-44- |
InChIKey | PQYYGKKQLURZNL-MEHBGYSTNA-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 | CCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)COP(O)(=O)OCC(COC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=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 |