6,7-EPOXY-5-BETA-ANDROSTANE-3,17-DIOL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | KNGRJDL73Pw |
|---|---|
| InChI | InChI=1S/C19H30O3/c1-18-7-5-10(20)9-13(18)16-17(22-16)15-11-3-4-14(21)19(11,2)8-6-12(15)18/h10-17,20-21H,3-9H2,1-2H3/t10-,11-,12-,13-,14-,15-,16+,17-,18+,19-/m0/s1 |
| InChIKey | ZHERNZILEBMHKG-QWWYLJFRSA-N |
| Mol Weight | 306.45 g/mol |
| Molecular Formula | C19H30O3 |
| Exact Mass | 306.219495 g/mol |
| Enantiomer InChIKey | ZHERNZILEBMHKG-VKTALHHZSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Hyocholic acid (HCA)
Cholestane-3,6,7-triol
Chenodeoxycholic acid-Sulfate (CDCA-S)
6-BETA-ACETOXY-5-ALPHA-CHOLESTAN-3-BETA-OL
5a-Cholestane-3b,6b-diol-6b-acetate
(3.alpha.,5.beta.,7.alpha.)-3,7-Bis(acetyloxy)-24-norcholan-23-oic acid
3α,7α-dihydroxy-5β-cholan-24-oic acid, methyl ester, 7-acetate
METHYL-3,7-DIACETYLCHENODESOXYCHOLATE
3α,7α-Dihydroxy-5β-cholan-24-oic acid, methyl ester, diacetate
Cholan-24-oic acid, 3,7-bis(acetyloxy)-, methyl ester, (3.alpha.,7.alpha.)-
| Title | Journal or Book | Year |
|---|---|---|
| Microbial hydroxylation of steroids. 9. Epoxidation of Δ6-3-ketosteroids by Rhizopusarrhizus ATCC 11145, and the mechanism of the 6β hydroxylase enzyme | Canadian Journal of Chemistry | 1984 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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