化学
磺胺
碳酸酐酶
组合化学
生物有机化学
酶
癌细胞
生物活性
生物化学
金属
细胞毒性
抗癌药
药品
结构-活动关系
水溶液中的金属离子
细胞
癌细胞系
立体化学
细胞周期检查点
肿瘤细胞
酶抑制
细胞周期
癌症
碳酸酐酶Ⅱ
微管蛋白
细胞培养
酶分析
药效团
药物发现
药理学
作者
Pandichamy J. Subhashini,Palanisamy Chandrabooma,M. Gowri
标识
DOI:10.1134/s1068162025602575
摘要
Sulfonamides, commonly known as sulfa drugs, are well-established anticancer agents whose activity is highly dependent on their substitution pattern. The anticancer activity of sulfonamide derivatives is mediated through several mechanisms of action, including the inhibition of carbonic anhydrase (CA) enzymes, cell cycle arrest at the G1 phase, and disruption of microtubule dynamics. Sulfonamides are also utilized as ligands for the synthesis of metal complexes with ions such as Ni(II), Cu(II), Co(II), Mn(II), Pb(II), Cd(II), Cr(III), Fe(III), Sn(II), and Sr(II). These complexes exhibit diverse biological activities, including radical scavenging, enzyme inhibition, as well as antifungal, antibacterial, and anticancer properties. Numerous complexes have been identified to demonstrate favorable activity against various cancer cell lines.
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