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携带苯磺酰胺片段的定制四取代咪唑作为选择性人碳酸酐酶 IX/XII 抑制剂。

Tailored Tetrasubstituted Imidazole Carrying the Benzenesulfonamide Fragments as Selective Human Carbonic Anhydrase IX/XII Inhibitors.

机构信息

Department of Basic Medical and Dental Sciences, Faculty of Dentistry, Zarqa University, Zarqa, 13110, Jordan.

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Al-Azhar University, Asyut, 71524, Assiut, Egypt.

出版信息

ChemMedChem. 2024 May 17;19(10):e202400004. doi: 10.1002/cmdc.202400004. Epub 2024 Mar 4.

Abstract

A new series of tetrasubstituted imidazole carrying sulfonamide as zinc-anchoring group has been designed. The structures of the synthesized derivatives 5 a-l have been confirmed by spectroscopic analysis. These compounds incorporate an ethylenic spacer between the benzenesulfonamide and the rest of the trisubstituted imidazole moiety and were tested as inhibitors of carbonic anhydrases and for in-vitro cytotoxicity. Most of them act as effective inhibitors of the tumor-linked CA isoforms IX and XII, in nanomolar range. Also, different compounds have shown selectivity in comparable with the standard acetazolamide. Our IBS 5 d, 5 g, and 5 l (with Ki: 10.1, 19.4, 19.8 nM against hCA IX and 47, 45, 20 nM against hCA IX) showed the best inhibitory profile. In-vitro screening of all derivatives against a full sixty-cell-lined from NCI at a single dose of 10 μM offered growth inhibition of up to 45 %. Compound 5 b has been identified with the most potent cytotoxic activity and broad spectrum. Docking studies have also been implemented and were also in accordance with the biological outcomes. Our SAR analysis has interestingly proposed efficient tumor-related hCAs IX/XII suppression.

摘要

已经设计了一系列带有磺酰胺作为锌锚定基团的四取代咪唑。通过光谱分析确认了合成衍生物 5a-l 的结构。这些化合物在苯磺酰胺和其余的三取代咪唑部分之间包含一个烯属间隔物,并被测试为碳酸酐酶抑制剂和体外细胞毒性。它们中的大多数在纳摩尔范围内作为肿瘤相关 CA 同工酶 IX 和 XII 的有效抑制剂起作用。此外,不同的化合物表现出与标准乙酰唑胺相当的选择性。我们的 IBS 5d、5g 和 5l(对 hCA IX 的 Ki 值分别为 10.1、19.4 和 19.8 nM,对 hCA IX 的 Ki 值分别为 47、45 和 20 nM)表现出最佳的抑制特性。所有衍生物在 10 μM 的单剂量下对 NCI 的六十个细胞系进行的体外筛选提供了高达 45%的生长抑制。化合物 5b 被鉴定具有最强的细胞毒性活性和广谱性。还进行了对接研究,并且也与生物学结果一致。我们的 SAR 分析有趣地提出了有效的肿瘤相关 hCAs IX/XII 抑制。

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