METHYL-(13S)-ENT-16-HYDROXY-3-OXO-8-ALPHA,13-EPOXY-LABD-14-EN-18-OATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | KEy5pEdmAln |
|---|---|
| InChI | InChI=1S/C21H32O5/c1-6-21(13-22)12-8-14-18(2)10-9-16(23)20(4,17(24)25-5)15(18)7-11-19(14,3)26-21/h6,14-15,22H,1,7-13H2,2-5H3/t14?,15?,18-,19-,20+,21+/m0/s1 |
| InChIKey | SPHXQRHQFUAXLN-GBIYJVTPSA-N |
| Mol Weight | 364.5 g/mol |
| Molecular Formula | C21H32O5 |
| Exact Mass | 364.224974 g/mol |
| Enantiomer InChIKey | SPHXQRHQFUAXLN-MRJAGOFRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-(13S)-ENT-3,16-DIOXO-8-ALPHA,13-EPOXY-LABD-14-EN-18-OATE
METHYL-(13S)-ENT-3-ALPHA,16-DIHYDROXY-8-ALPHA,13-EPOXY-LABD-14-EN-18-OATE
EXCOECARIN-R1-METHYLESTER
EXCOECARIN-R2-METHYLESTER
ent-12.alpha.Acetoxy-3-oxo-13-epi-manoyl oxide
METHYL-(13S)-ENT-1-BETA,16-DIHYDROXY-8-ALPHA,13-EPOXYLABD-14-EN-18-OATE
ENT-16,18-DIACETOXY-6-OXO-13-EPI-MANOYL-OXIDE
8-ALPHA,13-EPOXY-1,20-CYCLO-LABD-14-ENE-2-ONE-PARA-TOLUENESULFONYLHYDRAZONE
16,17.alpha.-epoxy-steviol - methyl ester
3.beta.-Acetoxy-11-oxo-5.beta.(H)-8(9)-etienic-acid Methylester
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of enantio-manoyl oxides: Modifiers of the activity of adenylatecyclase enzyme | Phytochemistry | 1995 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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