6-BETA,14-ALPHA-DIHYDROXY-PROGESTERONE
Compound with spectra: 3 NMR, and 1 MS (GC)
| SpectraBase Compound ID | JyBIhiU6czi |
|---|---|
| InChI | InChI=1S/C21H30O4/c1-12(22)14-6-9-21(25)16-11-18(24)17-10-13(23)4-7-19(17,2)15(16)5-8-20(14,21)3/h10,14-16,18,24-25H,4-9,11H2,1-3H3/t14-,15+,16-,18-,19-,20-,21-/m1/s1 |
| InChIKey | LQCNIUSTCXGYKI-PIABYFCUSA-N |
| Mol Weight | 346.47 g/mol |
| Molecular Formula | C21H30O4 |
| Exact Mass | 346.214409 g/mol |
| Enantiomer InChIKey | LQCNIUSTCXGYKI-DLQWHNFBSA-N |
| Copyright | Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Prof. Spiteller, University Bayreuth, Germany |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:CD3OD=1:1 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
- 6-BETA,14-ALPHA-DIHYDROXYPREGN-4-ENE-3,20-DIONE
- (6R,8R,9S,10R,13R,14R,17S)-17-acetyl-6,14-dihydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
- 6,14-DIHYDROXYPREGN-4-ENE-3,20-DIONE
| Title | Journal or Book | Year |
|---|---|---|
| Biotransformation of progesterone by Absidia griseolla var. igachii and Rhizomucor pusillus | Steroids | 2012 |
| Microbial transformation of steroids: Contribution to 14α-hydroxylations | Steroids | 1995 |
| New Hydroxylation Products of Progesterone with Mucor griseocyanus | Journal of Natural Products | 1987 |
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