RACEMOSALACTONE_A;5-ALPHA-HYDROXYEUDESM-11-(13)-EN-12,8-BETA-OLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 4t1RrUaAu6T |
|---|---|
| InChI | InChI=1S/C15H22O3/c1-9-5-4-6-14(3)8-12-11(7-15(9,14)17)10(2)13(16)18-12/h9,11-12,17H,2,4-8H2,1,3H3/t9-,11+,12+,14+,15+/m0/s1 |
| InChIKey | QZONJQGILMNCNE-LTDFUNFTSA-N |
| Mol Weight | 250.34 g/mol |
| Molecular Formula | C15H22O3 |
| Exact Mass | 250.156895 g/mol |
| Enantiomer InChIKey | QZONJQGILMNCNE-GIEZYDSUSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
10-BETA-HYDROXYEREMOPHILENOLIDE
NAPHTHO[2,3-B]FURAN-2(4H)ONE, 4A,5,6,7,8,8A,9,9A-OCTAHYDRO-8A-HYDROXY-3,4A,5-TRIMETHYL-
(8.alpha.-H)-10.beta.-hydroxyeremophilenolide
(1-S,5-S,7-R,8-S,10-R)-14-ACETOXY-4-OXOPSEUDOGUAI-11-(13)-EN-12,8-OLIDE
HYMENOLIDE,3-EPI
HYMENOLIDE
CARABROLACTONE_B
MICHAPANOLIDE
CUMAMBRIN B,8-DESOXY
10-EPI-8-DEOXYCUMAMBRIN
| Title | Journal or Book | Year |
|---|---|---|
| Structural Investigation and Biological Activity of Sesquiterpene Lactones from the Traditional Chinese Herb Inula racemosa | Journal of Natural Products | 2013 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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