Finasteride (Synonyms: MK-906) |
| Catalog No.GC16248 |
Finasteride(MK-906)는 유형 II 5α-환원효소에 대한 IC50이 4.2nM인 강력하고 경쟁력 있는 5α-환원효소 억제제입니다. Finasteride는 type I 효소보다 type II 5α-reductase 효소에 대해 약 100배 더 큰 친화력을 가지고 있습니다. 피나스테리드는 양성 전립선 비대증(BPH) 및 안드로겐 탈모증의 연구에 사용할 수 있습니다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 98319-26-7
Sample solution is provided at 25 µL, 10mM.
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Finasteride is an orally active testosterone 5-alpha-reductase inhibitor (Ki= 10 nM). Target: 5-alpha ReductaseApproved: 1992Finasteride, a synthetic 4-azasteroid antiandrogen compound, is a specific inhibitor of steroid Type II 5α-reductase, an intracellular enzyme that converts the androgen testosterone into 5α-dihydrotestosterone (DHT). Finasteride is used in the treatment of prostate cancer, benign prostatic hyperplasia, and androgenetic alopecia (male pattern baldness). In benign prostatic hyperplasia, finasteride inhibits 5alpha-reductase activity in epithelium for Ki of 10 nM, significantly lower than in stroma (Ki = 33nM) [1].
References:
[1]. Weisser, H. and M. Krieg, In vitro inhibition of androstenedione 5alpha-reduction by finasteride in epithelium and stroma of human benign prostatic hyperplasia. J Steroid Biochem Mol Biol, 1998. 67(1): p. 49-55.
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