Tandem optimization of target activity and elimination of mutagenic potential in a potent series of N-aryl bicyclic hydantoin-based selective androgen receptor modulators
作者:Lawrence G. Hamann、Mark C. Manfredi、Chongqing Sun、Stanley R. Krystek、Yanting Huang、Yingzhi Bi、David J. Augeri、Tammy Wang、Yan Zou、David. A. Betebenner、Aberra Fura、Ramakrishna Seethala、Rajasree Golla、Joyce E. Kuhns、John A. Lupisella、Celia J. Darienzo、Laura L. Custer、Jennifer L. Price、James M. Johnson、Scott A. Biller、Robert Zahler、Jacek Ostrowski
DOI:10.1016/j.bmcl.2007.01.076
日期:2007.4
Pharmacokinctic studies in cynomolgus monkeys with a novel prototype selective androgen receptor modulator revealed trace amounts of an aniline fragment released through hydrolytic metabolism. This aniline fragment was determined to be mutagenic in an Ames assay. subsequent concurrent optimization for target activity and avoidance of mutagenicity led to the identification of a pharmacologically superior clinical candidate without mutagenic potential. (c) 2007 Elsevier Ltd. All rights reserved.