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MLCL 20:5_22:4_24:5
SpectraBase Compound ID C9rVlm1zdtJ
InChI InChI=1S/C75H120O16P2/c1-4-7-10-13-16-19-22-25-28-31-33-34-36-39-40-43-46-49-52-55-58-61-73(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)63-60-57-54-51-48-45-42-37-30-27-24-21-18-15-12-9-6-3)68-86-74(79)62-59-56-53-50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,33-35,38-40,42,45,51,54,70-72,76-77H,4-6,13-15,22-24,31-32,36-37,41,43-44,46-50,52-53,55-69H2,1-3H3,(H,81,82)(H,83,84)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,34-33-,38-35-,40-39-,45-42-,54-51-
InChIKey GXNWJDAPPBZSGP-SOWCCIQSNA-N
Mol Weight 1339.7 g/mol
Molecular Formula C75H120O16P2
Exact Mass 1338.805162 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID Ks9CYD7mD2O
Name MLCL 20:5_22:4_24:5
Classification Glycerophospholipids [GP]
Comments Lysocardiolipin
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1338.805161764 u
Formula C75H120O16P2
InChI InChI=1S/C75H120O16P2/c1-4-7-10-13-16-19-22-25-28-31-33-34-36-39-40-43-46-49-52-55-58-61-73(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)63-60-57-54-51-48-45-42-37-30-27-24-21-18-15-12-9-6-3)68-86-74(79)62-59-56-53-50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,33-35,38-40,42,45,51,54,70-72,76-77H,4-6,13-15,22-24,31-32,36-37,41,43-44,46-50,52-53,55-69H2,1-3H3,(H,81,82)(H,83,84)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,34-33-,38-35-,40-39-,45-42-,54-51-
InChIKey GXNWJDAPPBZSGP-SOWCCIQSNA-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/CCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)COP(O)(=O)OCC(O)COC(=O)CCCCCCC\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