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HexCer 61:5;3O(FA 20:2)
SpectraBase Compound ID X5BCAu2Gba
InChI InChI=1S/C87H157NO10/c1-3-5-7-9-11-13-15-17-19-43-47-51-55-59-63-67-71-75-83(92)96-76-72-68-64-60-56-52-48-45-42-40-38-36-34-32-30-28-26-24-22-20-21-23-25-27-29-31-33-35-37-39-41-44-46-50-54-58-62-66-70-74-82(91)88-79(78-97-87-86(95)85(94)84(93)81(77-89)98-87)80(90)73-69-65-61-57-53-49-18-16-14-12-10-8-6-4-2/h11,13-14,16-17,19-21,24,26,53,57,69,73,79-81,84-87,89-90,93-95H,3-10,12,15,18,22-23,25,27-52,54-56,58-68,70-72,74-78H2,1-2H3,(H,88,91)/b13-11-,16-14+,19-17-,21-20-,26-24-,57-53+,73-69+
InChIKey STWCJQDXJBOFQL-VHFBVESQNA-N
Mol Weight 1377.2 g/mol
Molecular Formula C87H157NO10
Exact Mass 1376.18075 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

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SpectraBase Spectrum ID BRYzT4eKrk0
Name HexCer 61:5;3O(FA 20:2)
Classification Sphingolipids [SP]
Comments Hexosylceramide Esterified omega-hydroxy fatty acid-sphingosine
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1376.180750249 u
Formula C87H157NO10
InChI InChI=1S/C87H157NO10/c1-3-5-7-9-11-13-15-17-19-43-47-51-55-59-63-67-71-75-83(92)96-76-72-68-64-60-56-52-48-45-42-40-38-36-34-32-30-28-26-24-22-20-21-23-25-27-29-31-33-35-37-39-41-44-46-50-54-58-62-66-70-74-82(91)88-79(78-97-87-86(95)85(94)84(93)81(77-89)98-87)80(90)73-69-65-61-57-53-49-18-16-14-12-10-8-6-4-2/h11,13-14,16-17,19-21,24,26,53,57,69,73,79-81,84-87,89-90,93-95H,3-10,12,15,18,22-23,25,27-52,54-56,58-68,70-72,74-78H2,1-2H3,(H,88,91)/b13-11-,16-14+,19-17-,21-20-,26-24-,57-53+,73-69+
InChIKey STWCJQDXJBOFQL-VHFBVESQNA-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+CH3COO]-
SMILES CCCCCC\C=C\CC\C=C\CC\C=C\C(O)C(COC1OC(CO)C(O)C(O)C1O)NC(=O)CCCCCCCCCCCCCCCCCCC\C=C/C\C=C/CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC
Sample Comments theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES