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新型 4-(2-嘧啶基氨基)苯甲酰胺衍生物作为有效的 Hedgehog 信号通路抑制剂。

Novel 4-(2-pyrimidinylamino)benzamide derivatives as potent hedgehog signaling pathway inhibitors.

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Health Science Center, Xi'an Jiaotong University, No 76, Yanta West Road, Xi'an 710061, PR China.

Jiangsu Simcere Pharmaceutical Co. Ltd., No 699-18, Xuan Wu District, Nanjing 210042, PR China.

出版信息

Bioorg Med Chem. 2018 Oct 1;26(18):5029-5036. doi: 10.1016/j.bmc.2018.08.037. Epub 2018 Aug 31.

Abstract

A series of novel hedgehog signaling pathway inhibitors have been designed and synthesized based on our previously reported scaffold of 4-(2-pyrimidinylamino)benzamide. The Hh signaling pathway inhibitory activities were evaluated by Gli-luciferase reporter method and most compounds showed more potent inhibitory activities than vismodegib. Three compounds were picked out to evaluated in vivo for their PK properties, and compound 23b bearing a 2-pyridyl A-ring and (morpholin-4-yl)methylene at 3-position of D-ring demonstrated satisfactory PK properties. This study suggested the 4-(2-pyrimidinylamino)benzamides were a series of potent Hh signaling pathway inhibitors, deserving to further structural optimization.

摘要

基于我们之前报道的 4-(2-嘧啶基氨基)苯甲酰胺骨架,设计并合成了一系列新型 hedgehog 信号通路抑制剂。通过 Gli-荧光素酶报告基因法评估了 Hh 信号通路抑制活性,大多数化合物的抑制活性均强于 vismodegib。选择了三个化合物进行体内 PK 特性评价,其中带有 2-吡啶基 A 环和 D 环 3 位的 (吗啉-4-基)亚甲基的化合物 23b 表现出令人满意的 PK 特性。本研究表明 4-(2-嘧啶基氨基)苯甲酰胺是一系列有效的 Hedgehog 信号通路抑制剂,值得进一步的结构优化。

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