SpectraBase Compound ID | D9oB7MxLavd |
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InChI | InChI=1S/C73H116O16P2/c1-4-7-10-13-16-19-22-25-28-31-32-33-34-37-39-41-44-47-50-53-56-59-71(76)83-62-68(74)63-85-90(79,80)86-64-69(75)65-87-91(81,82)88-67-70(89-73(78)61-58-55-52-49-46-43-40-36-30-27-24-21-18-15-12-9-6-3)66-84-72(77)60-57-54-51-48-45-42-38-35-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,32-33,37-39,42,44,47-48,51,68-70,74-75H,4-6,13-15,22-24,31,34-36,40-41,43,45-46,49-50,52-67H2,1-3H3,(H,79,80)(H,81,82)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,33-32-,39-37-,42-38-,47-44-,51-48- |
InChIKey | MQPYODOIUJYMBY-AKNLWBRFNA-N |
Mol Weight | 1311.7 g/mol |
Molecular Formula | C73H116O16P2 |
Exact Mass | 1310.773862 g/mol |
SpectraBase Spectrum ID | 9vK0DSfvyYU |
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Name | MLCL 20:3_20:5_24:6 |
Classification | Glycerophospholipids [GP] |
Comments | Lysocardiolipin |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1310.773861635 u |
Formula | C73H116O16P2 |
InChI | InChI=1S/C73H116O16P2/c1-4-7-10-13-16-19-22-25-28-31-32-33-34-37-39-41-44-47-50-53-56-59-71(76)83-62-68(74)63-85-90(79,80)86-64-69(75)65-87-91(81,82)88-67-70(89-73(78)61-58-55-52-49-46-43-40-36-30-27-24-21-18-15-12-9-6-3)66-84-72(77)60-57-54-51-48-45-42-38-35-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,32-33,37-39,42,44,47-48,51,68-70,74-75H,4-6,13-15,22-24,31,34-36,40-41,43,45-46,49-50,52-67H2,1-3H3,(H,79,80)(H,81,82)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,33-32-,39-37-,42-38-,47-44-,51-48- |
InChIKey | MQPYODOIUJYMBY-AKNLWBRFNA-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 | CC\C=C/C\C=C/C\C=C/CCCCCCCCCC(=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(O)COC(=O)CCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC |
Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |