化学
对抗
天然产物
体内
敌手
受体
药理学
立体化学
反激动剂
结构-活动关系
毛茛
受体拮抗剂
化学合成
组胺H3受体
体外
生物化学
生物
中国仓鼠卵巢细胞
生物技术
作者
Vincent J. Santora,Jonathan A. Covel,Rena Hayashi,Brian Hofilena,Jason B. Ibarra,Michelle D. Pulley,Michael I. Weinhouse,Dipanjan Sengupta,Jonathan J. Duffield,Graeme Semple,Robert R. Webb,Carleton R. Sage,Albert Ren,Guilherme Rocha Pereira,Jens Knudsen,Jeffrey E. Edwards,Marissa Suarez,John Frazer,William Thomsen,Erin K. Hauser,Kevin Whelan,Andrew J. Grottick
标识
DOI:10.1016/j.bmcl.2007.12.059
摘要
A new family of Histamine H(3) receptor antagonists (5a-t) has been prepared based on the structure of the natural product Conessine, a known H(3) antagonist. Several members of the new series are highly potent and selective binders of rat and human H(3) receptors and display inverse agonism at the human H(3) receptor. Compound 5n exhibited promising rat pharmacokinetic properties and demonstrated functional antagonism of the H(3) receptor in an in-vivo pharmacological model.
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