EC Number   |
Title |
Organism |
|---|
    1.3.1.22 | 11alpha-Hydroxyprogesterone, a potent 11alpha-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5alpha-reductase and cytochrome P450 17alpha-hydroxylase/17,20-lyase to produce C11alpha-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro |
Homo sapiens |
| 1.3.1.22 | Anti-androgenic curcumin analogues as steroid 5-alpha reductase inhibitors |
Homo sapiens |
| 1.3.1.22 | Anti-androgenic curcumin analogues as steroid 5-alpha reductase inhibitors |
Homo sapiens CRL-1740 |
| 1.3.1.22 | Apigenin inhibits rat neurosteroidogenic 5alpha-reductase 1 and 3alpha-hydroxysteroid dehydrogenase |
Rattus norvegicus |
| 1.3.1.22 | Butylated hydroxyanisole alters rat 5alpha-reductase and 3alpha-hydroxysteroid dehydrogenase Implications for influences of neurosteroidogenesis |
Rattus norvegicus |
| 1.3.1.22 | Crystal structure of steroid reductase SRD5A reveals conserved steroid reduction mechanism |
Proteobacteria bacterium |
| 1.3.1.22 | Expression in Escherichia Coli, purification, and functional reconstitution of human steroid 5alpha-reductases |
Homo sapiens |
| 1.3.1.22 | Structure of human steroid 5alpha-reductase 2 with the anti-androgen drug finasteride |
Homo sapiens |
| 1.3.1.22 | Synthesis, biological evaluation and molecular docking of avicequinone C analogues as potential steroid 5alpha-reductase inhibitors |
Homo sapiens |
| 1.3.1.22 | 3,3-diphenylpentane skeleton as a steroid skeleton substitute: novel inhibitors of human 5alpha-reductase 1 |
Homo sapiens |
