SCLEROSTEROID-J;19-ACETOXY-3,3-DIMETHOXY-5-ALPHA-PREGN-20-ENE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 2AwY6AZPTA7 |
|---|---|
| InChI | InChI=1S/C25H40O4/c1-6-18-8-10-21-20-9-7-19-15-25(27-4,28-5)14-13-24(19,16-29-17(2)26)22(20)11-12-23(18,21)3/h6,18-22H,1,7-16H2,2-5H3/t18-,19-,20-,21-,22-,23+,24+/m0/s1 |
| InChIKey | ODFZDCGIBPRSKS-CLZKWMEGSA-N |
| Mol Weight | 404.6 g/mol |
| Molecular Formula | C25H40O4 |
| Exact Mass | 404.29266 g/mol |
| Enantiomer InChIKey | ODFZDCGIBPRSKS-OOJBBXMBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
5α-Androstan-3,3-dimethoxy-17β-ol hexahydrobenzoate
Spiro[1,3-benzodioxole-2,3'-cholestan]
17b,19-Diacetoxy-5a-homo-2a-oxa-5b-androstan-3-one
3 .beta.,(20R)-diacetoxy-18-azido-5 .alpha.-pregnane
19-ACETOXY-3-ALPHA-AMINO-5-ALPHA-CHOLESTANE
19-ACETOXY-3-ALPHA-AMINO-5-BETA-CHOLESTANE
5.beta.-Androstan-3-one, 17.beta.,19-dihydroxy-, diacetate
3,3-Ethylenedioxycholanic acid, methyl ester
17b,19-Diacetoxy-5a-homo-3a-oxa-5b-androstan-3-one
(4R)-4-[(3R,5R,8S,9S,10R,13R,14S,17R)-13-methyl-3-trimethylsilyloxy-10-(trimethylsilyloxymethyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoic acid methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Cytotoxic and Anti-Inflammatory Metabolites from the Soft Coral Scleronephthya gracillimum | Marine Drugs | 2013 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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