26-HYDROXY-4,22-STIGMASTA-DIEN-3-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 7Dsl31zzslP |
|---|---|
| InChI | InChI=1S/C29H46O2/c1-6-21(20(3)18-30)8-7-19(2)25-11-12-26-24-10-9-22-17-23(31)13-15-28(22,4)27(24)14-16-29(25,26)5/h7-8,17,19-21,24-27,30H,6,9-16,18H2,1-5H3/b8-7+/t19-,20?,21-,24+,25-,26+,27+,28?,29?/m1/s1 |
| InChIKey | CXBBDQPWEBLECH-KUCAVLBKSA-N |
| Mol Weight | 426.7 g/mol |
| Molecular Formula | C29H46O2 |
| Exact Mass | 426.349781 g/mol |
| Enantiomer InChIKey | CXBBDQPWEBLECH-JMUOGMLSSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
4,22-Cholestadien-24β-ethyl-3-one
(24R)-24-METHYLCHOLEST-4,22E-DIEN-3-ONE
26,27-Dinorergosta-4,22-dien-3-one, (22E)-
(22E,24-ALPHA)-24-ETHYL-3-OXO-CHOLESTA-4,22(23)-DIEN-25-OL
(22E)-STIGMASTA-4,22,25-TRIEN-3-ONA
3-OXO-4,22-ERGOSTA-DIEN-26-OIC-ACID-METHYLESTER
(22Z)-Cholesta-4,22-dien-3-one
No Name
(8S,9S,10R,13S,14S,17S)-17-[(1S)-1-methoxyethyl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
20-DEOXO-20-ACETOXYMETHYL-PROGESTERONE
| Title | Journal or Book | Year |
|---|---|---|
| Microbial transformation of β-sitosterol and stigmasterol into 26-oxygenated derivatives | Steroids | 1995 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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