Ivanova Jekateri Na, Nocentini Alessio, Ta Rs Kaspars, Leita Ns Ja Nis, Dvinskis Elviss, Kazaks Andris, Domračeva Ilona, Supuran Claudiu T, Žalubovskis Raivis
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.
J Med Chem. 2023 Apr 27;66(8):5703-5718. doi: 10.1021/acs.jmedchem.3c00007. Epub 2023 Apr 6.
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.
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。