11β-Hydroxyprogesterone
Compound with spectra: 6 NMR, 4 FTIR, and 1 MS (GC)
| SpectraBase Compound ID | 32sqb7PN3Ce |
|---|---|
| InChI | InChI=1S/C21H30O3/c1-12(22)16-6-7-17-15-5-4-13-10-14(23)8-9-20(13,2)19(15)18(24)11-21(16,17)3/h10,15-19,24H,4-9,11H2,1-3H3/t15-,16+,17-,18-,19+,20-,21+/m0/s1 |
| InChIKey | BFZHCUBIASXHPK-ATWVFEABSA-N |
| Mol Weight | 330.47 g/mol |
| Molecular Formula | C21H30O3 |
| Exact Mass | 330.219495 g/mol |
| Enantiomer InChIKey | BFZHCUBIASXHPK-WQNFENHCSA-N |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Q3270-000 |
| Copyright | Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Aldrich |
| Catalog Number | 286206 |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | J. J. Schneider, Jefferson Medical Center, Philadelphia, Pennsylvania |
| Technique | KBr WAFER |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | John J. Schneider, Jefferson Medical College, Philadelphia, Pennsylvania |
| Technique | KBr WAFER |
| 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 | DMSO |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:DMSO-D6 |
| 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 |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 286206 |
| Solvent | CDCl3 |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 286206 |
| Solvent | CDCl3 |
- 11β-Hydroxy-4-pregnen-3,20-dione
- 11-BETA-HYDROXYPREGN-4-EN-3,20-DION
- PROGESTERONE, 11B-HYDROXY-,
- PREGN-4-ENE-3,20-DIONE, 11B-HYDROXY-,
- 11-Hydroxypregn-4-ene-3,20-dione
- 11.BETA.-HYDROXY-PREGN-4-ENE-3,20-DIONE
- 11beta-Hydroxy-4-pregnene-3,20-dione, 11beta-Hydroxypregn-4-ene-3,20-dione, 4-Pregnen-11beta-ol-3,20-dione
- (8S,9S,10R,11S,13S,14S,17S)-17-acetyl-11-hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one
11-BETA-FLUOROPREGN-4-ENE-3,20-DIONE
11.beta.,20-Dihydroxy-3-oxopregn-4-en-21-al
11 β-hydroxycholest-4-en-3-one
11α,20β,21-trihydroxypregn-4-en-3-one
11β,20β,21-trihydroxypregn-4-en-3-one
11 β, 20 α, 21-trihydroxypregn-4-en-3-one
11b-Hydroxy-1,4-pregnadiene-3,20-dione
(8S,9S,10R,13S,14S,17S)-17-acetyl-11-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
(11-alpha,16-beta)-11,16-dihydroxypregna-4-ene-3-one
11alpha,15beta-dihydroxy-4-pregnene-3,20-dione
| Title | Journal or Book | Year |
|---|---|---|
| An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila | The Journal of Steroid Biochemistry and Molecular Biology | 2009 |
| A carbon‐13 nuclear magnetic resonance study of the 1,4‐diene analogues of steroid hormones and related steroids | Organic Magnetic Resonance | 1984 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
| Substituent effects in carbon-13 nuclear magnetic resonance spectroscopy. Progesterone, deoxycorticosterone, corticosterone, cortisol, and related steroids | Journal of the American Chemical Society | 1973 |