GnRH receptor antagonists are disclosed that 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
2a
, R
2b
, R
3
, R
4
, R
5
, R
6
and X are as defined herein, including stereoisomers, prodrugs 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GnRH受体拮抗剂,其在治疗男性和女性的各种性激素相关疾病中具有用途。本发明的化合物具有以下结构:其中R1a,R1b,R1c,R2a,R2b,R3,R4,R5,R6和X如本文所定义,包括立体异构体,前药和其药物可接受的盐。还揭示了含有本发明化合物的组合物与药物可接受的载体的组合物,以及与此有关的方法,用于在需要拮抗
促性腺激素释放激素的受体的个体中使用。