Suppr超能文献

Atropo/Tropo灵活性:一种用于设计和合成碳酸酐酶自适应抑制剂及其抗增殖作用的工具。

Atropo/Tropo Flexibility: A Tool for Design and Synthesis of Self-Adaptable Inhibitors of Carbonic Anhydrases and Their Antiproliferative Effect.

作者信息

Ivanova Jekateri Na, Nocentini Alessio, Ta Rs Kaspars, Leita Ns Ja Nis, Dvinskis Elviss, Kazaks Andris, Domračeva Ilona, Supuran Claudiu T, Žalubovskis Raivis

机构信息

Latvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.

NEUROFARBA Department, Sezione di Scienze Farmaceutiche, University of Florence, Via Ugo Schiff 6, Sesto Fiorentino, 50019 Florence, Italy.

出版信息

J Med Chem. 2023 Apr 27;66(8):5703-5718. doi: 10.1021/acs.jmedchem.3c00007. Epub 2023 Apr 6.

Abstract

Here, we report for the first time a series of sulfonamide derivatives with scaffolds bearing flexible moieties, namely, rotamers or tropoisomers capable of adapting their geometry in the active center of enzymes thus being effective and selective carbonic anhydrase (CAs, EC 4.2.1.1) enzyme inhibitors. All compounds exhibited effective in vitro inhibition activity toward the main hCA isoforms related to cancer (i.e., hCA II, hCA IX, and hCA XII with values in the low nanomolar range). Three selected compounds showed a great cytotoxic effect on cancer cell lines ex vivo. X-ray crystallographic experiments assessed the binding modes of compound with active centers of hCA IX and hCA XII.

摘要

在此,我们首次报道了一系列具有带有柔性部分支架的磺酰胺衍生物,即能够在酶的活性中心改变其几何形状的旋转异构体或扭转异构体,因此它们是有效的和选择性的碳酸酐酶(CAs,EC 4.2.1.1)酶抑制剂。所有化合物对与癌症相关的主要hCA同工型(即hCA II、hCA IX和hCA XII,其值在低纳摩尔范围内)均表现出有效的体外抑制活性。三种选定的化合物在体外对癌细胞系显示出极大的细胞毒性作用。X射线晶体学实验评估了化合物与hCA IX和hCA XII活性中心的结合模式。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验