SpectraBase Compound ID | 2dNL3equ35V |
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InChI | InChI=1S/C74H114O6/c1-4-7-10-13-16-19-22-25-28-29-30-31-32-33-34-35-36-37-38-39-40-41-42-43-44-45-47-49-52-55-58-61-64-67-73(76)79-70-71(69-78-72(75)66-63-60-57-54-51-48-27-24-21-18-15-12-9-6-3)80-74(77)68-65-62-59-56-53-50-46-26-23-20-17-14-11-8-5-2/h7-8,10-11,16-17,19-20,24-28,30-31,33-34,36-37,39-40,42-43,45-47,52-53,55-56,71H,4-6,9,12-15,18,21-23,29,32,35,38,41,44,48-51,54,57-70H2,1-3H3/b10-7-,11-8-,19-16-,20-17-,27-24-,28-25-,31-30-,34-33-,37-36-,40-39-,43-42-,46-26-,47-45-,55-52-,56-53- |
InChIKey | JBFDWLRXXHXLPC-CZCDRSHBNA-N |
Mol Weight | 1099.7 g/mol |
Molecular Formula | C74H114O6 |
Exact Mass | 1098.861541 g/mol |
SpectraBase Spectrum ID | TjRyJHhnNx |
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Name | TG 17:1_18:4_36:10 |
Classification | Glycerolipids [GL] |
Comments | Triacylglyceride |
Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
Exact Mass | 1098.861541385 u |
Formula | C74H114O6 |
InChI | InChI=1S/C74H114O6/c1-4-7-10-13-16-19-22-25-28-29-30-31-32-33-34-35-36-37-38-39-40-41-42-43-44-45-47-49-52-55-58-61-64-67-73(76)79-70-71(69-78-72(75)66-63-60-57-54-51-48-27-24-21-18-15-12-9-6-3)80-74(77)68-65-62-59-56-53-50-46-26-23-20-17-14-11-8-5-2/h7-8,10-11,16-17,19-20,24-28,30-31,33-34,36-37,39-40,42-43,45-47,52-53,55-56,71H,4-6,9,12-15,18,21-23,29,32,35,38,41,44,48-51,54,57-70H2,1-3H3/b10-7-,11-8-,19-16-,20-17-,27-24-,28-25-,31-30-,34-33-,37-36-,40-39-,43-42-,46-26-,47-45-,55-52-,56-53- |
InChIKey | JBFDWLRXXHXLPC-CZCDRSHBNA-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 | CCCCCCC\C=C/CCCCCCCC(=O)OCC(COC(=O)CCCC\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/C\C=C/CC)OC(=O)CCCC\C=C/C\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 |