6-Azasteroids: structure-activity relationships for inhibition of type 1 and 2 human 5 alpha-reductase and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase

• Published in: Journal of medicinal chemistry Vol. 37; no. 15; pp. 2352 - 2360
• Main Authors: Frye, S V, Haffner, C D, Maloney, P R, Mook, Jr, R A, Dorsey, Jr, G F, Hiner, R N, Cribbs, C M, Wheeler, T N, Ray, J A, Andrews, R C
• Format: Journal Article
• Language: English
• Published: United States 22.07.1994
• Subjects: 3-Hydroxysteroid Dehydrogenases - antagonists & inhibitors; 5-alpha Reductase Inhibitors; Adrenal Glands - enzymology; Animals; Azasteroids - chemistry; Azasteroids - pharmacology; Dogs; Humans; Isoenzymes - antagonists & inhibitors; Rats; Rats, Sprague-Dawley; Steroid Isomerases - antagonists & inhibitors; Structure-Activity Relationship
• ISSN: 0022-2623; 1520-4804

6-Azaandrost-4-en-3-ones were synthesized and tested versus human type 1 and 2 steroid 5 alpha-reductase (5AR) and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase (3BHSD) to explore the structure-activity relationship of this novel series in order to optimize potency versus both isozymes of 5AR and selectivity versus 3BHSD. Compounds with picomolar IC50's versus human type 2 5AR and low nanomolar Ki's versus human type 1 5AR with 100-fold selectivity versus 3BHSD were identified (70). Preliminary in vivo evaluation of some optimal compounds from this series in a chronic castrated rat model of 5AR inhibitor-induced prostate involution and dog pharmacokinetic measurements identified a series of 17 beta-[N-(diphenylmethyl)carbamoyl]-6-azaandrost-4-en-3-ones (compounds 54, 66, and 67) with good in vivo efficacy and half-life in the dog. Inhibitors with, at the minimum, low nanomolar potency toward both human 5AR's and selectivity versus 3BHSD may show advantages over previously known 5AR inhibitors in the treatment of disease states which depend upon dihydrotestosterone, such as benign prostatic hyperplasia.