SpectraBase Compound ID | LF8KEARSAXH |
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InChI | InChI=1S/C76H122O6/c1-4-7-10-13-16-19-22-25-27-29-31-32-33-34-35-36-37-38-39-40-41-42-43-44-45-47-48-51-54-57-60-63-66-69-75(78)81-72-73(71-80-74(77)68-65-62-59-56-53-50-24-21-18-15-12-9-6-3)82-76(79)70-67-64-61-58-55-52-49-46-30-28-26-23-20-17-14-11-8-5-2/h7,9-10,12,16,18-19,21,25,27-28,30-32,34-35,37-38,40-41,43-44,47-48,50,53,73H,4-6,8,11,13-15,17,20,22-24,26,29,33,36,39,42,45-46,49,51-52,54-72H2,1-3H3/b10-7-,12-9-,19-16-,21-18-,27-25-,30-28-,32-31-,35-34-,38-37-,41-40-,44-43-,48-47-,53-50- |
InChIKey | NKVYYZUIHCBGBL-WNHUKOOCNA-N |
Mol Weight | 1131.8 g/mol |
Molecular Formula | C76H122O6 |
Exact Mass | 1130.924142 g/mol |
SpectraBase Spectrum ID | JvIcGYWFfrJ |
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Name | TG 16:3_21:1_36:9 |
Classification | Glycerolipids [GL] |
Comments | Triacylglyceride |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1130.924141642 u |
Formula | C76H122O6 |
InChI | InChI=1S/C76H122O6/c1-4-7-10-13-16-19-22-25-27-29-31-32-33-34-35-36-37-38-39-40-41-42-43-44-45-47-48-51-54-57-60-63-66-69-75(78)81-72-73(71-80-74(77)68-65-62-59-56-53-50-24-21-18-15-12-9-6-3)82-76(79)70-67-64-61-58-55-52-49-46-30-28-26-23-20-17-14-11-8-5-2/h7,9-10,12,16,18-19,21,25,27-28,30-32,34-35,37-38,40-41,43-44,47-48,50,53,73H,4-6,8,11,13-15,17,20,22-24,26,29,33,36,39,42,45-46,49,51-52,54-72H2,1-3H3/b10-7-,12-9-,19-16-,21-18-,27-25-,30-28-,32-31-,35-34-,38-37-,41-40-,44-43-,48-47-,53-50- |
InChIKey | NKVYYZUIHCBGBL-WNHUKOOCNA-N |
Ion Polarity | P |
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+Na]+ |
SMILES | CCCCCCCCC\C=C/CCCCCCCCCC(=O)OC(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)COC(=O)CCCCC\C=C/C\C=C/C\C=C/CC |
Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |