For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.
LNAPS 26:7/N-26:1
SpectraBase Compound ID 15FIWZAZFeg
InChI InChI=1S/C58H98NO10P/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/h6,8,12,14,17-20,24,26,30,32,36,38,42,44,54-55,60H,3-5,7,9-11,13,15-16,21-23,25,27-29,31,33-35,37,39-41,43,45-53H2,1-2H3,(H,59,61)(H,63,64)(H,65,66)/b8-6-,14-12-,19-17+,20-18-,26-24-,32-30-,38-36-,44-42-
InChIKey XCUACQNDRNQDEH-JVOJOGSBNA-N
Mol Weight 1000.4 g/mol
Molecular Formula C58H98NO10P
Exact Mass 999.692835 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

View the Full Spectrum for FREE!

The full spectrum can only be viewed using a FREE account.

SpectraBase Spectrum ID La2J9Vy8NvD
Name LNAPS 26:7/N-26:1
Classification Glycerophosphoserines [GP03]
Comments N-acyl-lysophosphatidylserine
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 999.692835348 u
Formula C58H98NO10P
InChI InChI=1S/C58H98NO10P/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/h6,8,12,14,17-20,24,26,30,32,36,38,42,44,54-55,60H,3-5,7,9-11,13,15-16,21-23,25,27-29,31,33-35,37,39-41,43,45-53H2,1-2H3,(H,59,61)(H,63,64)(H,65,66)/b8-6-,14-12-,19-17+,20-18-,26-24-,32-30-,38-36-,44-42-
InChIKey XCUACQNDRNQDEH-JVOJOGSBNA-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 CCCCCCCC\C=C\CCCCCCCCCCCCCCCC(=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