SpectraBase Compound ID | lGLhXwBXwh |
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InChI | InChI=1S/C101H168O16P2/c1-4-7-10-13-16-19-22-25-28-31-33-35-37-39-41-43-45-46-47-48-50-52-53-55-57-59-61-64-66-69-72-75-78-81-84-87-99(104)111-90-96(102)91-113-118(107,108)114-92-97(103)93-115-119(109,110)116-95-98(117-101(106)89-86-83-80-77-74-71-68-63-30-27-24-21-18-15-12-9-6-3)94-112-100(105)88-85-82-79-76-73-70-67-65-62-60-58-56-54-51-49-44-42-40-38-36-34-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,33-36,39-42,45-46,68,71,77,80,96-98,102-103H,4-6,13-15,22-24,31-32,37-38,43-44,47-67,69-70,72-76,78-79,81-95H2,1-3H3,(H,107,108)(H,109,110)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,35-33-,36-34-,41-39-,42-40-,46-45-,71-68-,80-77- |
InChIKey | ZUKFHMUOSKPZFW-RBIIYDNPNA-N |
Mol Weight | 1700.4 g/mol |
Molecular Formula | C101H168O16P2 |
Exact Mass | 1699.180763 g/mol |
SpectraBase Spectrum ID | LrQ1hDXavmY |
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Name | MLCL 20:5_34:5_38:6 |
Classification | Glycerophospholipids [GP] |
Comments | Lysocardiolipin |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1699.180763310 u |
Formula | C101H168O16P2 |
InChI | InChI=1S/C101H168O16P2/c1-4-7-10-13-16-19-22-25-28-31-33-35-37-39-41-43-45-46-47-48-50-52-53-55-57-59-61-64-66-69-72-75-78-81-84-87-99(104)111-90-96(102)91-113-118(107,108)114-92-97(103)93-115-119(109,110)116-95-98(117-101(106)89-86-83-80-77-74-71-68-63-30-27-24-21-18-15-12-9-6-3)94-112-100(105)88-85-82-79-76-73-70-67-65-62-60-58-56-54-51-49-44-42-40-38-36-34-32-29-26-23-20-17-14-11-8-5-2/h7-12,16-21,25-30,33-36,39-42,45-46,68,71,77,80,96-98,102-103H,4-6,13-15,22-24,31-32,37-38,43-44,47-67,69-70,72-76,78-79,81-95H2,1-3H3,(H,107,108)(H,109,110)/b10-7-,11-8-,12-9-,19-16-,20-17-,21-18-,28-25-,29-26-,30-27-,35-33-,36-34-,41-39-,42-40-,46-45-,71-68-,80-77- |
InChIKey | ZUKFHMUOSKPZFW-RBIIYDNPNA-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/CCCCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)COP(O)(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCCC\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 |