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MLCL 22:6_30:5_32:6
SpectraBase Compound ID EKdJx04fFIw
InChI InChI=1S/C93H150O16P2/c1-4-7-10-13-16-19-22-25-28-31-34-36-38-40-42-43-45-47-48-50-53-55-58-61-64-67-70-73-76-79-91(96)103-82-88(94)83-105-110(99,100)106-84-89(95)85-107-111(101,102)108-87-90(109-93(98)81-78-75-72-69-66-63-60-57-52-33-30-27-24-21-18-15-12-9-6-3)86-104-92(97)80-77-74-71-68-65-62-59-56-54-51-49-46-44-41-39-37-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,34-37,40-42,44-45,47,52,57,63,66,72,75,88-90,94-95H,4-6,13-15,22-24,31-33,38-39,43,46,48-51,53-56,58-62,64-65,67-71,73-74,76-87H2,1-3H3,(H,99,100)(H,101,102)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,36-34-,37-35-,42-40-,44-41-,47-45-,57-52-,66-63-,75-72-
InChIKey JRSIGMBJDGQSOF-DCJNXKNMNA-N
Mol Weight 1586.2 g/mol
Molecular Formula C93H150O16P2
Exact Mass 1585.039913 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID Gi2xWTBLsPR
Name MLCL 22:6_30:5_32:6
Classification Glycerophospholipids [GP]
Comments Lysocardiolipin
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1585.039912730 u
Formula C93H150O16P2
InChI InChI=1S/C93H150O16P2/c1-4-7-10-13-16-19-22-25-28-31-34-36-38-40-42-43-45-47-48-50-53-55-58-61-64-67-70-73-76-79-91(96)103-82-88(94)83-105-110(99,100)106-84-89(95)85-107-111(101,102)108-87-90(109-93(98)81-78-75-72-69-66-63-60-57-52-33-30-27-24-21-18-15-12-9-6-3)86-104-92(97)80-77-74-71-68-65-62-59-56-54-51-49-46-44-41-39-37-35-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,34-37,40-42,44-45,47,52,57,63,66,72,75,88-90,94-95H,4-6,13-15,22-24,31-33,38-39,43,46,48-51,53-56,58-62,64-65,67-71,73-74,76-87H2,1-3H3,(H,99,100)(H,101,102)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,36-34-,37-35-,42-40-,44-41-,47-45-,57-52-,66-63-,75-72-
InChIKey JRSIGMBJDGQSOF-DCJNXKNMNA-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/CCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)COP(O)(=O)OCC(O)COC(=O)CCCCCCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=O)CC\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