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Ac4PIM2 18:1_16:1_18:0(methyl)_19:0
SpectraBase Compound ID CYc3GW2fjo9
InChI InChI=1S/C93H171O25P/c1-6-10-14-18-22-25-28-31-33-35-38-41-44-47-55-61-67-79(98)115-88-84(103)85(104)89(116-92-86(105)82(101)80(99)74(68-94)113-92)91(90(88)117-93-87(106)83(102)81(100)75(114-93)71-110-77(96)65-59-53-49-48-51-57-63-72(5)62-56-50-21-17-13-9-4)118-119(107,108)111-70-73(69-109-76(95)64-58-52-45-42-39-36-30-27-24-20-16-12-8-3)112-78(97)66-60-54-46-43-40-37-34-32-29-26-23-19-15-11-7-2/h26,29,36,39,72-75,80-94,99-106H,6-25,27-28,30-35,37-38,40-71H2,1-5H3,(H,107,108)/b29-26-,39-36-
InChIKey GPWIXDKIQZKGSP-CYEKLCOOSA-N
Mol Weight 1720.3 g/mol
Molecular Formula C93H171O25P
Exact Mass 1719.184708 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID GzSd34QRVzY
Name Ac4PIM2 18:1_16:1_18:0(methyl)_19:0
Classification Glycerophospholipids [GP]
Comments Tetraacylated phosphatidylinositol dimannoside
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1719.184707979 u
Formula C93H171O25P
InChI InChI=1S/C93H171O25P/c1-6-10-14-18-22-25-28-31-33-35-38-41-44-47-55-61-67-79(98)115-88-84(103)85(104)89(116-92-86(105)82(101)80(99)74(68-94)113-92)91(90(88)117-93-87(106)83(102)81(100)75(114-93)71-110-77(96)65-59-53-49-48-51-57-63-72(5)62-56-50-21-17-13-9-4)118-119(107,108)111-70-73(69-109-76(95)64-58-52-45-42-39-36-30-27-24-20-16-12-8-3)112-78(97)66-60-54-46-43-40-37-34-32-29-26-23-19-15-11-7-2/h26,29,36,39,72-75,80-94,99-106H,6-25,27-28,30-35,37-38,40-71H2,1-5H3,(H,107,108)/b29-26-,39-36-
InChIKey GPWIXDKIQZKGSP-CYEKLCOOSA-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.CCCCCC\C=C/CCCCCCCCCC(=O)O%10.CCCCCCCC\C=C/CCCCCC(=O)O%11.CCCCCCCCC(C)CCCCCCCCC(=O)O%12.CCCCCCCCCCCCCCCCCCC(=O)O%13
Sample Comments theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES