SpectraBase Compound ID | GHtv9sKt3yW |
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InChI | InChI=1S/C75H118O16P2/c1-4-7-10-13-16-19-22-25-28-31-32-33-34-35-36-39-41-43-46-49-52-55-58-61-73(78)85-64-70(76)65-87-92(81,82)88-66-71(77)67-89-93(83,84)90-69-72(91-75(80)63-60-57-54-51-48-45-42-38-30-27-24-21-18-15-12-9-6-3)68-86-74(79)62-59-56-53-50-47-44-40-37-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,32-33,35-36,40-45,50,53,70-72,76-77H,4-6,13-15,22-24,31,34,37-39,46-49,51-52,54-69H2,1-3H3,(H,81,82)(H,83,84)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,33-32-,36-35-,43-41-,44-40-,45-42-,53-50- |
InChIKey | ZZUDPRDXSMSDSK-HQLXWJFTNA-N |
Mol Weight | 1337.7 g/mol |
Molecular Formula | C75H118O16P2 |
Exact Mass | 1336.789512 g/mol |
SpectraBase Spectrum ID | H5EM6YZU75B |
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Name | MLCL 20:4_20:5_26:6 |
Classification | Glycerophospholipids [GP] |
Comments | Lysocardiolipin |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1336.789511700 u |
Formula | C75H118O16P2 |
InChI | InChI=1S/C75H118O16P2/c1-4-7-10-13-16-19-22-25-28-31-32-33-34-35-36-39-41-43-46-49-52-55-58-61-73(78)85-64-70(76)65-87-92(81,82)88-66-71(77)67-89-93(83,84)90-69-72(91-75(80)63-60-57-54-51-48-45-42-38-30-27-24-21-18-15-12-9-6-3)68-86-74(79)62-59-56-53-50-47-44-40-37-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,32-33,35-36,40-45,50,53,70-72,76-77H,4-6,13-15,22-24,31,34,37-39,46-49,51-52,54-69H2,1-3H3,(H,81,82)(H,83,84)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,33-32-,36-35-,43-41-,44-40-,45-42-,53-50- |
InChIKey | ZZUDPRDXSMSDSK-HQLXWJFTNA-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/C\C=C/CCCCCCC(=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)CCCCCC\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 |