作者:Greta Varchi、Andrea Guerrini、Anna Tesei、Giovanni Brigliadori、Carlo Bertucci、Marzia Di Donato、Gabriella Castoria
DOI:10.1021/ml3000269
日期:2012.6.14
We report herein a stereoselective and straightforward methodology for the synthesis of new androgen receptor ligands with (anti)-agonistic activities. Oxygen nitrogen replacement in bicalutamide-like structures paves the way to the disclosure of a new class of analogues, including cyclized/nitrogen-substituted derivatives, with promising antiandrogen (or anabolic) activity.