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合成及某些新型苯甲酰胺衍生物的 Smo 活性。

Synthesis and Smo Activity of Some Novel Benzamide Derivatives.

机构信息

Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.

出版信息

Molecules. 2017 Dec 31;23(1):85. doi: 10.3390/molecules23010085.

Abstract

Two series of benzamides compounds bearing piperidine groups were synthesized and the Gli-luc luciferase activity was screened by Gys-luc luciferase gene detection method. Compound showed promising inhibition of hedgehog (Hh) signaling pathway. To further verify whether the Hh inhibitory activities of the target compounds are derived from their inhibition to the Smoothened (Smo) receptor, the compounds with good potency were evaluated in a fluorescence competitive displacement assays, the results showed the Smo inhibitory potency of these compounds correlated well with their Hh inhibition, which suggested that the observed Hh activity was driven by Smo inhibitors.

摘要

合成了两个系列含哌啶基团的苯甲酰胺化合物,并通过 Gys-luc 荧光素酶基因检测方法筛选 Gli-luc 荧光素酶活性。化合物 显示出对 Hedgehog(Hh)信号通路有很好的抑制作用。为了进一步验证目标化合物的 Hh 抑制活性是否源于对 Smoothened(Smo)受体的抑制作用,对具有良好活性的化合物进行了荧光竞争置换测定,结果表明这些化合物对 Smo 的抑制活性与其对 Hh 的抑制活性密切相关,这表明观察到的 Hh 活性是由 Smo 抑制剂驱动的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43dc/6017536/5744a5caaf9b/molecules-23-00085-g001.jpg

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