首页> 外文期刊>Bioorganic and medicinal chemistry >Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyra zol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist.
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Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyra zol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist.

机译:2-(4-((1H-1,2,4-三唑-1-基)甲基)-5-(4-溴苯基)-1-(2-氯苯基)-1H-吡唑-3-基的发现)-5-叔丁基-1,3,4-噻二唑(GCC2680)作为有效,选择性和口服有效的大麻素1受体拮抗剂。

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摘要

Structure-activity relationship studies in a series of diarylpyrazolyl thiadiazoles identified cannabinoid-1 receptor antagonists with excellent potency and selectivity. Based on its exceptional in vivo efficacy in animal models and its favorable pharmacokinetic and toxicological profiles, 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyra zol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) was selected as a preclinical candidate for the treatment of obesity.
机译:在一系列二芳基吡唑基噻二唑中进行的构效关系研究确定了大麻素-1受体拮抗剂具有出色的效能和选择性。 2-(4-(((1H-1,2,4-triazol-1-yl)methyl)-5-(4-溴苯基)-选择1-(2-氯苯基)-1H-吡唑-3-基)-5-叔丁基-1,3,4-噻二唑(GCC2680)作为治疗肥胖的临床前候选药物。

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