Novel Dihydropyrimidinone Derivatives as Potential P-Glycoprotein Modulators.

Novel Dihydropyrimidinone Derivatives as Potential P-Glycoprotein Modulators.
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DOI:
10.1021/acsomega.1c05839
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发表时间:
2022-05-17
期刊:
影响因子:
4.1
通讯作者:
Radadiya, Ashish
Radadiya, Ashish
中科院分区:
化学3区
文献类型:
--
作者:
Bijani, Sabera;Shaikh, Faraz;Mirza, Sheefa;Siu, Shirley Weng In;Jain, Nayan;Rawal, Rakesh;Richards, Nigel G. J.;Shah, Anamik;Radadiya, Ashish

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P-糖蛋白 (Pgp) 是一种 ATP 结合盒 (ABC) 转运蛋白,是一种 ATP 依赖性外排泵,负责癌症多药耐药性。作为鉴定人类 Pgp (hPgp) 抑制剂的努力的一部分,我们使用非常适合获得化合物库的合成方法制备了一系列新型三唑缀合的二氢嘧啶酮。这些二氢嘧啶酮衍生物中的几种以低微摩尔 EC50 值调节人 P-糖蛋白 (hPgp) 活性。分子对接研究表明这些化合物与转运蛋白的 M 位点结合。
P-glycoprotein (Pgp), an ATP binding cassette (ABC) transporter, is an ATP-dependent efflux pump responsible for cancer multidrug resistance. As part of efforts to identify human Pgp (hPgp) inhibitors, we prepared a series of novel triazole-conjugated dihydropyrimidinones using a synthetic approach that is well suited for obtaining compound libraries. Several of these dihydropyrimidinone derivatives modulate human P-glycoprotein (hPgp) activity with low micromolar EC50 values. Molecular docking studies suggest that these compounds bind to the M-site of the transporter.
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