| 4-Hydroxytestosterone | |
|---|---|
| IUPAC name |
4,17-Dihydroxy-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one
|
| Other names | 4,17β-Dihydroxy-4-androstene-3-one; (17β)-4,17-dihydroxyandrost-4-en-3-one |
| Identifiers | |
| CAS number | 2141-17-5 |
| PubChem | 160615 |
| SMILES |
O=C4C(\O)=C2/[C@]([C@H]1CC[C@@]3([C@@H](O)CC[C@H]3[C@@H]1CC2)C)(C)CC4
|
| InChI |
1/C19H28O3/c1-18-10-8-15(20)17(22)14(18)4-3-11-12-5-6-16(21)19(12,2)9-7-13(11)18/h11-13,16,21-22H,3-10H2,1-2H3/t11-,12-,13-,16-,18+,19-/m0/s1
|
| InChI key | BQOIJSIMMIDHMO-FBPKJDBXBD |
| ChemSpider ID | 141138 |
| Properties | |
| Molecular formula | C19H28O3 |
| Molar mass | 304.42 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
4-Hydroxytestosterone (4-OHT or 4,17beta-dihydroxy-4-androstene-3-one) is an anabolic steroid. It was first patented by G.D. Searle & Company in 1955 and is testosterone with a hydroxy group at the four position. 4-OHT has moderate anabolic, mild androgenic, and anti-aromatic properties and is similar to the steroid clostebol.
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