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合成和生物评价设计为新型有效转位蛋白配体的 4-苯基喹唑啉-2-甲酰胺。

Synthesis and biological evaluation of 4-phenylquinazoline-2-carboxamides designed as a novel class of potent ligands of the translocator protein.

机构信息

Dipartimento di Scienze Farmaceutiche e Biomediche, Università di Salerno, Via Ponte Don Melillo, 84084 Fisciano (SA), Italy.

出版信息

J Med Chem. 2012 May 10;55(9):4506-10. doi: 10.1021/jm201703k. Epub 2012 Apr 25.

Abstract

A series of novel 4-phenylquinazoline-2-carboxamides (1-58) were designed as aza-isosters of PK11195, the well-known 18 kDa translocator protein (TSPO) reference ligand, and synthesized by means of a very simple and efficient procedure. A number of these derivatives bind to the TSPO with K(i) values in the nanomolar/subnanomolar range, show selectivity toward the central benzodiazepine receptor (BzR) and exhibit structure-affinity relationships consistent with a previously published pharmacophore/topological model of ligand-TSPO interaction.

摘要

一系列新型 4-苯基喹唑啉-2-甲酰胺(1-58)被设计为 PK11195 的氮杂类似物,PK11195 是一种著名的 18 kDa 移位蛋白(TSPO)参考配体,并通过非常简单高效的方法合成。这些衍生物中的许多与 TSPO 结合的 K(i) 值在纳摩尔/亚纳摩尔范围内,对中枢苯二氮䓬受体(BzR)具有选择性,并表现出与先前发表的配体-TSPO 相互作用的药效团/拓扑模型一致的结构-亲和力关系。

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