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Ac4PIM2 18:0(methyl)_16:1_16:1_18:0
SpectraBase Compound ID Fe350fE1bDP
InChI InChI=1S/C90H165O25P/c1-6-10-14-18-22-25-28-31-32-35-38-41-44-51-58-64-76(95)112-85-81(100)82(101)86(113-89-83(102)79(98)77(96)71(65-91)110-89)88(87(85)114-90-84(103)80(99)78(97)72(111-90)68-107-74(93)62-56-50-43-40-37-34-30-27-24-20-16-12-8-3)115-116(104,105)108-67-70(66-106-73(92)61-55-49-42-39-36-33-29-26-23-19-15-11-7-2)109-75(94)63-57-52-46-45-48-54-60-69(5)59-53-47-21-17-13-9-4/h33-34,36-37,69-72,77-91,96-103H,6-32,35,38-68H2,1-5H3,(H,104,105)/b36-33-,37-34-
InChIKey BVEDZMQJCTWIHD-HXDMKDIESA-N
Mol Weight 1678.3 g/mol
Molecular Formula C90H165O25P
Exact Mass 1677.137758 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID 4m3ejfgfJv
Name Ac4PIM2 18:0(methyl)_16:1_16:1_18:0
Classification Glycerophospholipids [GP]
Comments Tetraacylated phosphatidylinositol dimannoside
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1677.137757786 u
Formula C90H165O25P
InChI InChI=1S/C90H165O25P/c1-6-10-14-18-22-25-28-31-32-35-38-41-44-51-58-64-76(95)112-85-81(100)82(101)86(113-89-83(102)79(98)77(96)71(65-91)110-89)88(87(85)114-90-84(103)80(99)78(97)72(111-90)68-107-74(93)62-56-50-43-40-37-34-30-27-24-20-16-12-8-3)115-116(104,105)108-67-70(66-106-73(92)61-55-49-42-39-36-33-29-26-23-19-15-11-7-2)109-75(94)63-57-52-46-45-48-54-60-69(5)59-53-47-21-17-13-9-4/h33-34,36-37,69-72,77-91,96-103H,6-32,35,38-68H2,1-5H3,(H,104,105)/b36-33-,37-34-
InChIKey BVEDZMQJCTWIHD-HXDMKDIESA-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 OCC1OC(OC2C(O)C(O)C%13C(OC3OC(C%12)C(O)C(O)C3O)C2OP(O)(=O)OCC%10C%11)C(O)C(O)C1O.CCCCCCCCC(C)CCCCCCCCC(=O)O%10.CCCCCCCC\C=C/CCCCCC(=O)O%11.CCCCCCCC\C=C/CCCCCC(=O)O%12.CCCCCCCCCCCCCCCCCC(=O)O%13
Sample Comments theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES