8-BETA-HYDROXY-9-ALPHA-METHACRYLOYLOXY-14-OXO-ACANTHOSPERMOLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 4wckJXNR4ez |
|---|---|
| InChI | InChI=1S/C19H22O6/c1-10(2)18(22)25-17-13(9-20)7-5-6-11(3)8-14-15(16(17)21)12(4)19(23)24-14/h7-9,14-17,21H,1,4-6H2,2-3H3/b11-8-,13-7-/t14-,15+,16+,17+/m1/s1 |
| InChIKey | WJBPCLXXPBZSBC-VRPNJRMNSA-N |
| Mol Weight | 346.38 g/mol |
| Molecular Formula | C19H22O6 |
| Exact Mass | 346.141638 g/mol |
| Enantiomer InChIKey | WJBPCLXXPBZSBC-IDDAPHDDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
LECOCARPINOLIDE_E
LECOCARPINOLIDE E
ACANTHOLIDE
9-BETA,10-BETA-DIHYDROXY-8-BETA-ISOPROPYLOXY-GERMACRADIEN-6,7-OLIDE
1-ALPHA-HYDROXYACETYLIRINOL-4-ALPHA,5-BETA-EPOXIDE
GERMACRA-4E,10(14),11(13)-TRIEN-12,6-A-OLIDE,1-OXO-8-B-(4',5'-O-ISOPROPYLIDENETIGLOYLOXY)
EUPACHINILIDE-J;8-BETA-(4ï-ACETOXY-ANGELYLOXY)-2-ALPHA,3-BETA-DIHYDROXY-6-BETA-H,7-ALPHA-H-GERMARCA-1(10)-4-E,11(13)-TRIENE-6,12-OLIDE
No Name
CAUDATOL;COMFORMER_1
CAUDATOL-A
| Title | Journal or Book | Year |
|---|---|---|
| Study of sesquiterpene lactones from Milleria quinqueflora on their anti-inflammatory activity using the transcription factor NF-κB as molecular target | Phytochemistry | 2000 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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