MK-434
Подписчиков: 0, рейтинг: 0
| Clinical data | |
|---|---|
| Other names | MK-0434; 17β-Benzoyl-4-aza-5α-androst-1-en-3-one |
| Routes of administration |
By mouth |
| Drug class | 5α-Reductase inhibitor |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| Chemical and physical data | |
| Formula | C25H31NO2 |
| Molar mass | 377.528 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
MK-434 is a 5α-reductase inhibitor which was under development in the 1990s by Merck & Co for the treatment of a variety of androgen-dependent conditions including benign prostatic hyperplasia, prostate cancer, pattern hair loss, excessive hair growth, acne, and seborrhea but was never marketed. It acts as a selective inhibitor of 5α-reductase type 2. The drug has been found to decrease circulating dihydrotestosterone levels by a maximum of approximately 50% in men. MK-434 is a synthetic 4-azasteroid and is structurally related to other 5α-reductase inhibitors like finasteride.