DEOXYCORTICOSTERONE-21-O-BETA-GLUCOPYRANOSIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Aq2sawvL2vx |
|---|---|
| InChI | InChI=1S/C27H40O8/c1-26-9-7-15(29)11-14(26)3-4-16-17-5-6-19(27(17,2)10-8-18(16)26)20(30)13-34-25-24(33)23(32)22(31)21(12-28)35-25/h11,16-19,21-25,28,31-33H,3-10,12-13H2,1-2H3/t16-,17-,18-,19+,21+,22+,23-,24+,25+,26-,27-/m0/s1 |
| InChIKey | SMSMUZPFFJLROV-LARVYCNESA-N |
| Mol Weight | 492.6 g/mol |
| Molecular Formula | C27H40O8 |
| Exact Mass | 492.272318 g/mol |
| Enantiomer InChIKey | SMSMUZPFFJLROV-YWLRALPDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(8S,9S,10R,13S,14S,17S)-17-[2-(3-Hydroxy-naphthalen-2-ylmethoxy)-acetyl]-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one
20,21-Dihydroxypregna-4,20-dien-3-one, cyclic carbonate
1-(Pregn-4-en-3-on-20a-yl).beta.-D-glucopyranoside
TESTOSTERYL-2,6-DIDEOXY-2-IODO-ALPHA-D-MANNO-HEXOPYRANOSIDE
21-(Acetyloxy)-19-[(methanesulfonyl)oxy]-pregn-4-ene-3,20-dione
19-(Acetylsulfanyl)-21-(acetoxy)pregnane-3,20-dione
(25R)-26-IODINE-CHOLEST-4-EN-3,16,22-TRIONE
(25R)-16-HYDROXY-4-CHOLESTEN-3,22-DIONE-26-AL
ETHYL-3-KETO-20R-HYDROXY-23-NORCHOL-4-EN-24-OATE
3-Keto-20R-hydroxy-23-norchol-4-en-24-oic acid, ethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Biotransformation of 21-O-acetyl-deoxycorticosterone by cell suspension cultures of Digitalis lanata (strain W.1.4) | Steroids | 2012 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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