22-HYDROXY-CLEROSTEROL;(3-BETA,24S)-STIGMASTA-5,25-DIENE-3,22-DIOL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | AuwQubJY5SV |
|---|---|
| InChI | InChI=1S/C29H48O2/c1-7-20(18(2)3)16-27(31)19(4)24-10-11-25-23-9-8-21-17-22(30)12-14-28(21,5)26(23)13-15-29(24,25)6/h8,19-20,22-27,30-31H,2,7,9-17H2,1,3-6H3/t19-,20-,22-,23-,24+,25-,26-,27?,28-,29+/m0/s1 |
| InChIKey | RCCAVDWSAAMGOP-FIVAUHATSA-N |
| Mol Weight | 428.7 g/mol |
| Molecular Formula | C29H48O2 |
| Exact Mass | 428.365431 g/mol |
| Enantiomer InChIKey | RCCAVDWSAAMGOP-NDGJMDHSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
CHOLEST-5-ENE-3-BETA,22R-DIOL
(3beta,22R)-cholesta-5,24-diene-3,22-diol
MURICEANOL
24-Methylenecholesterol -24(28)-epoxide [muriceanol]
(22R,24R)-22,24-Dimethylcholesterol
(22R,24S)-22,24-Dimethylcholesterol
22(R)-methylcholesterol
(22S,23Z)-Cholesta-5,23-diene-3.beta.,22-diol
22,23-Methylene-cholestene-3-ol;4th diastereomer
22,23-Cyclopropane-cholesterol
| Title | Journal or Book | Year |
|---|---|---|
| Preparation Antitrypanosomal and Cytotoxic Activities of 22-Hydroxyclerosterol, a New Sterol from Allexis cauliflora (Violaceae) | Scientia Pharmaceutica | 2011 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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