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11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Suppliers list
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| | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Basic information |
| Product Name: | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one | | Synonyms: | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one;(8S,9S,10R,11R,13S,14S,17S)-11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one;11.alpha.-hydroxy Testosterone (DEA Schedule III);Androst-4-en-3-one, 11,17-dihydroxy-, (11α,17β)-;11α-hydroxy Testosterone;4-ANDROSTEN-11α, 17β-DIOL-3-ONE | | CAS: | 3066-12-4 | | MF: | C19H28O3 | | MW: | 304.42 | | EINECS: | | | Product Categories: | | | Mol File: | 3066-12-4.mol | ![11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Structure](CAS/GIF/3066-12-4.gif) |
| | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Chemical Properties |
| Melting point | 168-172 °C(Solvent: Acetone) | | Boiling point | 476.171±45.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.194±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | solubility | Ethanol: 1 mg/ml | | form | A crystalline solid | | pka | 14.562±0.70(predicted) |
| | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Usage And Synthesis |
| Description | 11α-hydroxy Testosterone is a metabolite of testosterone, produced by the cytochrome P450 (CYP) isoform CYP3A. It can also be generated from testosterone by a mutant of CYP107A1 and from 11α-hydroxy progesterone by the fungus B. bassiana. The biological activity of this metabolite has not been elucidated. | | Uses | 11α-Hydroxytestosterone is a deriviative of Hydrocortisone (HY-N0583), with the relative binding affinity to progesterone receptor of 9% (comparing to R5020 (HY-119384) 100%). 11α-Hydroxytestosterone inhibits the growth and differentiation of human decidual cells in culture[1]. | | Definition | ChEBI: 11alpha,17beta-Dihydroxyandrost-4-en-3-one is a 3-hydroxy steroid. It has a role as an androgen. | | References | [1] Q Zhao, et al. Synthesis of l 1-substituted androstenediones and testosterones as human decidual cell growth inhibitors. Steroids. 1994 Mar;59(3):190-5. DOI:10.1016/0039-128x(94)90027-2 |
| | 11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Preparation Products And Raw materials |
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