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MLCL 22:4_26:5_28:6
SpectraBase Compound ID DGsRHok9d2P
InChI InChI=1S/C85H138O16P2/c1-4-7-10-13-16-19-22-25-28-31-34-36-38-39-41-43-45-47-50-53-56-59-62-65-68-71-83(88)95-74-80(86)75-97-102(91,92)98-76-81(87)77-99-103(93,94)100-79-82(101-85(90)73-70-67-64-61-58-55-52-49-44-33-30-27-24-21-18-15-12-9-6-3)78-96-84(89)72-69-66-63-60-57-54-51-48-46-42-40-37-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,34-37,39,41-42,44-47,49,80-82,86-87H,4-6,13-15,22-24,31-33,38,40,43,48,50-79H2,1-3H3,(H,91,92)(H,93,94)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,36-34-,37-35-,41-39-,46-42-,47-45-,49-44-
InChIKey LRBXAVWPLQVYII-DQXXIIEFNA-N
Mol Weight 1478.0 g/mol
Molecular Formula C85H138O16P2
Exact Mass 1476.946012 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID JbHRa2Vr8wD
Name MLCL 22:4_26:5_28:6
Classification Glycerophospholipids [GP]
Comments Lysocardiolipin
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1476.946012344 u
Formula C85H138O16P2
InChI InChI=1S/C85H138O16P2/c1-4-7-10-13-16-19-22-25-28-31-34-36-38-39-41-43-45-47-50-53-56-59-62-65-68-71-83(88)95-74-80(86)75-97-102(91,92)98-76-81(87)77-99-103(93,94)100-79-82(101-85(90)73-70-67-64-61-58-55-52-49-44-33-30-27-24-21-18-15-12-9-6-3)78-96-84(89)72-69-66-63-60-57-54-51-48-46-42-40-37-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,34-37,39,41-42,44-47,49,80-82,86-87H,4-6,13-15,22-24,31-33,38,40,43,48,50-79H2,1-3H3,(H,91,92)(H,93,94)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,36-34-,37-35-,41-39-,46-42-,47-45-,49-44-
InChIKey LRBXAVWPLQVYII-DQXXIIEFNA-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)OC(COC(=O)CCCCCCCCC\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)CCCCCCCC\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