(1-S,5-S,7-R,8-S,10-R)-14-ACETOXY-4-OXOPSEUDOGUAI-11-(13)-EN-12,8-OLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | DM6nFdP6NdK |
|---|---|
| InChI | InChI=1S/C17H22O5/c1-9-12-7-17(3)13(4-5-15(17)19)11(8-21-10(2)18)6-14(12)22-16(9)20/h11-14H,1,4-8H2,2-3H3/t11-,12+,13-,14-,17-/m0/s1 |
| InChIKey | UGZPAZLOJSSVQY-WLZFUECHSA-N |
| Mol Weight | 306.36 g/mol |
| Molecular Formula | C17H22O5 |
| Exact Mass | 306.146724 g/mol |
| Enantiomer InChIKey | UGZPAZLOJSSVQY-QFRSUPTLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Azuleno[6,5-b]furan-2,5-dione, decahydro-7-hydroxy-4a,8-dimethyl-3-methylene-, [3aR-(3a.alpha.,4a.beta.,7.alpha.,7a.alpha.,8.beta.,9a.alpha.)]-
HYMENOLIDE
HYMENOLIDE,3-EPI
11,13-Methylene-graveolide
HYMENOXON,3-EPI
HYMENOXON
4-ACETOXYRUDMOLLIN
RUDMOLLIN,4-ACETOXY
(5R,6R,7R,8S,10S)-8-HYDROXY-15-OXOELEMA-1,3,11(13)-TRIEN-12,6-OLIDE
NNGUPYFWMPFAEX-BKKKSXESSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Pseudoguaianolides and Guaianolides from Inula hupehensis as Potential Anti-inflammatory Agents | Journal of Natural Products | 2011 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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