| SpectraBase Compound ID | Gm7jhYiaQ5S |
|---|---|
| InChI | InChI=1S/C58H88NO10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39-41-43-45-47-49-56(61)59-55(58(63)64)53-69-70(65,66)68-52-54(60)51-67-57(62)50-48-46-44-42-40-38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h5-8,11-14,17-20,23-26,29-32,35-38,42,44,54-55,60H,3-4,9-10,15-16,21-22,27-28,33-34,39-41,43,45-53H2,1-2H3,(H,59,61)(H,63,64)(H,65,66)/b7-5-,8-6-,13-11-,14-12-,19-17-,20-18-,25-23-,26-24-,31-29-,32-30-,37-35-,38-36-,44-42- |
| InChIKey | ZWDNHJUQGKRTQP-CQEVPTEZNA-N |
| Mol Weight | 990.3 g/mol |
| Molecular Formula | C58H88NO10P |
| Exact Mass | 989.614585 g/mol |
Mass Spectrum (LC)
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| SpectraBase Spectrum ID | 5sUmgWTKQ2L |
|---|---|
| Name | LNAPS 26:7/N-26:6 |
| Classification | Glycerophosphoserines [GP03] |
| Comments | N-acyl-lysophosphatidylserine |
| Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
| Exact Mass | 989.614585026 u |
| Formula | C58H88NO10P |
| InChI | InChI=1S/C58H88NO10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39-41-43-45-47-49-56(61)59-55(58(63)64)53-69-70(65,66)68-52-54(60)51-67-57(62)50-48-46-44-42-40-38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h5-8,11-14,17-20,23-26,29-32,35-38,42,44,54-55,60H,3-4,9-10,15-16,21-22,27-28,33-34,39-41,43,45-53H2,1-2H3,(H,59,61)(H,63,64)(H,65,66)/b7-5-,8-6-,13-11-,14-12-,19-17-,20-18-,25-23-,26-24-,31-29-,32-30-,37-35-,38-36-,44-42- |
| InChIKey | ZWDNHJUQGKRTQP-CQEVPTEZNA-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/C\C=C/CCCCCCC(=O)NC(COP(O)(=O)OCC(O)COC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)C(O)=O |
| Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |