(3S,5S,8R,9S,10S,13S,14S,17S)-3-HYDROXY-10,13-DIMETHYLOCTADECAHYDROSPIRO-[CYCLOPENTA-[A]-PHENANTHRENE-17,2'-PYRAN]-6'-(3'H)-ONE
Compound with spectra: 1 NMR
![(3S,5S,8R,9S,10S,13S,14S,17S)-3-HYDROXY-10,13-DIMETHYLOCTADECAHYDROSPIRO-[CYCLOPENTA-[A]-PHENANTHRENE-17,2'-PYRAN]-6'-(3'H)-ONE](/api/compound/3zT3mllj723.png?ph=true&h=300&w=458 "(3S,5S,8R,9S,10S,13S,14S,17S)-3-HYDROXY-10,13-DIMETHYLOCTADECAHYDROSPIRO-[CYCLOPENTA-[A]-PHENANTHRENE-17,2'-PYRAN]-6'-(3'H)-ONE")
| SpectraBase Compound ID | 3zT3mllj723 |
|---|---|
| InChI | InChI=1S/C23H36O3/c1-21-11-7-16(24)14-15(21)5-6-17-18(21)8-12-22(2)19(17)9-13-23(22)10-3-4-20(25)26-23/h15-19,24H,3-14H2,1-2H3/t15-,16-,17+,18-,19-,21-,22-,23-/m0/s1 |
| InChIKey | AYWCZDDJRAHCCG-SIKLISJLSA-N |
| Mol Weight | 360.5 g/mol |
| Molecular Formula | C23H36O3 |
| Exact Mass | 360.266445 g/mol |
| Enantiomer InChIKey | AYWCZDDJRAHCCG-IOFYVBRTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(5S,8R,9S,10S,13S,14S,17S)-10,13-DIMETHYLHEXADECAHYDROSPIRO-[CYCLOPENTA-[A]-PHENANTHRENE-17,2'-PYRAN]-3,6'-(2H,3'H)-DIONE
(5S,8R,9S,10S,13S,14S,17R)-5',10,13-TRIMETHYLHEXADECAHYDROSPIRO-[CYCLOPENTA-[A]-PHENANTHRENE-17,2'-PYRAN]-3,6'-(2H,3'H)-DIONE
17, 20β-epoxy-5β-pregnan-3 α-ol
17,20α-epoxy-5β-pregnan-3α-ol
3.beta.-[(Dimethylphenylsilyl)oxy]-17-(ethylenedioxy)-5.alpha.-androstane
17-ALPHA-[(N-4-AZIDO-2-NITROPHENYL)-AMINOPROPYL]-5-ALPHA-ANDROSTANE-3-BETA,17-BETA-DIOL
epimeric spiro[17-.beta.-Hydroxy-5'-iodomethyl-5.alpha.-androstan-17,2'-tetrahydrofuran]
5β-pregnane-3α,17,21-triol, 3,21-diacetate
17-ALPHA-[(N-4-AZIDO-2-NITROPHENYL)-AMINOETHYL]-5-ALPHA-ANDROSTANE-3-BETA,17-BETA-DIOL
3α,17,21-trihydroxy-5β-pregnan-20-one
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of 5α-Androstane-17-spiro-δ-lactones with a 3-Keto, 3-Hydroxy, 3-Spirocarbamate or 3-Spiromorpholinone as Inhibitors of 17β-Hydroxysteroid Dehydrogenases | Molecules | 2013 |