GnRH receptor antagonists are disclosed which have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R
1a
, R
1b
, R
1c
, R
1d
, R
2
, R
2a
, and A are as defined herein, including stereoisomers, esters, solvates, and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
本发明揭示了具有在男性和女性中治疗各种性激素相关疾病用途的GnRH受体拮抗剂。本发明的化合物具有以下结构:其中R1a,R1b,R1c,R1d,R2,R2a和A如此定义,包括立体异构体,
酯类,溶剂化物和其药学上可接受的盐。还揭示了含有本发明化合物与药学上可接受的载体结合的组合物,以及与其相关的用于在需要时拮抗
促性腺激素释放激素的方法。