(25R)-26-IODINE-CHOLEST-4-EN-3,16,22-TRIONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 56FDeEIdKLL |
|---|---|
| InChI | InChI=1S/C27H39IO3/c1-16(15-28)5-8-23(30)17(2)25-24(31)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h13,16-17,20-22,25H,5-12,14-15H2,1-4H3/t16-,17-,20-,21+,22+,25+,26+,27+/m1/s1 |
| InChIKey | NHMVKIXGNOZZOH-AMSGTRTDSA-N |
| Mol Weight | 538.5 g/mol |
| Molecular Formula | C27H39IO3 |
| Exact Mass | 538.19439 g/mol |
| Enantiomer InChIKey | NHMVKIXGNOZZOH-PBDNZBRZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(25R)-16-HYDROXY-4-CHOLESTEN-3,22-DIONE-26-AL
20-S-ACETYLOXY-4-PREGNENE-3,16-DIONE
Cholest-5-ene-16,22-dione, 3,26-bis(acetyloxy)-, (3.beta.,25R)-
Trimethylsilyl ether of 4-Pregnene-16.alpha.-ol-3,20-one
DEOXYCORTICOSTERONE-21-O-BETA-GLUCOPYRANOSIDE
16-ALPHA-ALLYL-PROGESTERONE
2H-Naphth[2',1':4,5]indeno[1,2-d][1,3,2]dioxaborole, androst-4-en-3-one deriv.
1-(Pregn-4-en-3-on-20a-yl).beta.-D-glucopyranoside
ZXOWRHGFYZFWFE-VZRBKJHWSA-N
16-ALPHA-ETHYL-PROGESTERONE
| Title | Journal or Book | Year |
|---|---|---|
| Diosgenone Synthesis, Anti-Malarial Activity and QSAR of Analogues of This Natural Product | Molecules | 2013 |
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.