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1-烷基-苯并三唑-5-羧酸是人类孤儿G蛋白偶联受体GPR109b的高度选择性激动剂。

1-Alkyl-benzotriazole-5-carboxylic acids are highly selective agonists of the human orphan G-protein-coupled receptor GPR109b.

作者信息

Semple Graeme, Skinner Philip J, Cherrier Martin C, Webb Peter J, Sage Carleton R, Tamura Susan Y, Chen Ruoping, Richman Jeremy G, Connolly Daniel T

出版信息

J Med Chem. 2006 Feb 23;49(4):1227-30. doi: 10.1021/jm051099t.

Abstract

1-Substituted benzotriazole carboxylic acids have been identified as the first reported examples of selective small-molecule agonists of the human orphan G-protein-coupled receptor GPR109b (HM74), a low-affinity receptor for the HDL-raising drug niacin. No activity was observed at the highly homologous high-affinity niacin receptor GPR109a (HM74A). The high degree of selectivity was attributed to a difference in the amino acid sequence adjacent to a key arginine-ligand interaction allowing somewhat larger ligands to be tolerated by GPR109b.

摘要

1-取代苯并三唑羧酸已被确定为人类孤儿G蛋白偶联受体GPR109b(HM74)的首批报道的选择性小分子激动剂实例,GPR109b是提高高密度脂蛋白(HDL)的药物烟酸的低亲和力受体。在高度同源的高亲和力烟酸受体GPR109a(HM74A)上未观察到活性。高度的选择性归因于与关键精氨酸-配体相互作用相邻的氨基酸序列差异,这使得GPR109b能够耐受稍大一些的配体。

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