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MLCL 20:5_20:5_24:6
SpectraBase Compound ID EFeGJHnSnd
InChI InChI=1S/C73H112O16P2/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/h7-12,16-21,25-30,32-33,37-40,42-44,47-49,51-52,68-70,74-75H,4-6,13-15,22-24,31,34-36,41,45-46,50,53-67H2,1-3H3,(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-,43-40-,47-44-,51-48-,52-49-
InChIKey MDXPQHOPAXXYFK-IAAXWGNONA-N
Mol Weight 1307.6 g/mol
Molecular Formula C73H112O16P2
Exact Mass 1306.742562 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID 7616lncAsqg
Name MLCL 20:5_20:5_24:6
Classification Glycerophospholipids [GP]
Comments Lysocardiolipin
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1306.742561506 u
Formula C73H112O16P2
InChI InChI=1S/C73H112O16P2/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/h7-12,16-21,25-30,32-33,37-40,42-44,47-49,51-52,68-70,74-75H,4-6,13-15,22-24,31,34-36,41,45-46,50,53-67H2,1-3H3,(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-,43-40-,47-44-,51-48-,52-49-
InChIKey MDXPQHOPAXXYFK-IAAXWGNONA-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/C\C=C/CCCC(=O)OCC(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)OC(=O)CCC\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