Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Ege University, 35100 Bornova, İzmir, Turkey.
Università degli Studi di Firenze, Laboratorio di Chimica Bioinorganica, Rm. 188, Via Della Lastruccia 3, I-50019 Sesto Fiorentino (Firenze), Italy.
Bioorg Chem. 2020 Oct;103:104236. doi: 10.1016/j.bioorg.2020.104236. Epub 2020 Aug 26.
This study reports the design, synthesis of a series of taurine containing benzenesulfonamide derivatives which were all screened in vitro against the physiological relevant human (h) expressed Carbonic Anhydrase (CA; EC 4.2.1.1) I, II, IX, XII isozymes. Compound 2, 5, 11-16 displayed superior inhibitory activities against the tumor associated hCA IX over the reference drug Acetazolamide (AAZ). Both hCA IX and XII isoforms were selectively inhibited only by compound 3, whereas the chloro-containing compound 12 was showed as the most selective and effective inhibitor profile for the CA IX isoforms. To the best of our knowledge the data reported herein are the first of this kind and introduce in the literature new compounds worth for future development within the Medicinal Chemistry field.
本研究报告了一系列含牛磺酸的苯磺酰胺衍生物的设计和合成,这些化合物均在体外针对生理相关的人(h)表达的碳酸酐酶(CA;EC 4.2.1.1)同工酶 I、II、IX、XII 进行了筛选。化合物 2、5、11-16 对肿瘤相关的 hCA IX 的抑制活性优于参考药物乙酰唑胺(AAZ)。只有化合物 3 对 hCA IX 和 XII 同工酶具有选择性抑制作用,而含氯的化合物 12 则对 CA IX 同工酶表现出最具选择性和有效的抑制作用。据我们所知,本文所报道的数据是此类研究中的首例,为未来在药物化学领域的发展引入了新的值得研究的化合物。