3-BETA-ACETOXY-16-BETA-[4-(3-AMINOPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
Compound with spectra: 1 NMR
![3-BETA-ACETOXY-16-BETA-[4-(3-AMINOPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL](/api/compound/GY5n1dAEHPy.png?ph=true&h=300&w=458 "3-BETA-ACETOXY-16-BETA-[4-(3-AMINOPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL")
| SpectraBase Compound ID | GY5n1dAEHPy |
|---|---|
| InChI | InChI=1S/C30H40N4O3/c1-18(35)37-23-9-11-29(2)21(15-23)7-8-24-25(29)10-12-30(3)26(24)14-20(28(30)36)16-34-17-27(32-33-34)19-5-4-6-22(31)13-19/h4-7,13,17,20,23-26,28,36H,8-12,14-16,31H2,1-3H3/t20-,23+,24-,25+,26+,28+,29+,30+/m1/s1 |
| InChIKey | KYMBUMISYIJNLJ-RAEVXBBGSA-N |
| Mol Weight | 504.7 g/mol |
| Molecular Formula | C30H40N4O3 |
| Exact Mass | 504.310041 g/mol |
| Enantiomer InChIKey | KYMBUMISYIJNLJ-HSCDLODYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
3-BETA-ACETOXY-16-BETA-(4-PHENYL-1H-1,2,3-TRIAZOL-1-YLMETHYL)-ANDROST-5-EN-17-BETA-OL
3-BETA-ACETOXY-16-BETA-[4-(3-TOLYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
3-BETA-ACETOXY-16-BETA-[4-(4-FLUOROPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
3-BETA-ACETOXY-16-BETA-[4-(4-ETHYLPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
3-BETA-ACETOXY-16-BETA-[4-(4-TERT.-BUTYLPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
3-BETA-ACETOXY-16-BETA-(4-CYCLOPROPYL-1H-1,2,3-TRIAZOL-1-YLMETHYL)-ANDROST-5-EN-17-BETA-OL
(16R) Ethyl 3,16-diacetoxy-20-methyl-24-nor-chol-5-en-23-oate
16-ALPHA-ACETYLOXYMETHYL-ANDROST-5-EN-3-BETA-17-ALPHA-DIOLACETATE
3,17a-Diacetoxy-16a-methyleneacetoxy.delta. 5(6)-androsten
16-BETA-(ACETYLOXYMETHYL)-ANDROST-5-EN-3-BETA-17-BETA-DIOLACETATE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and In Vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives | Molecules | 2011 |