Sirajuddin Muhammad, Ali Saqib
Department of Chemistry, University of Science & Technology Bannu, 28100, Pakistan.
Curr Pharm Des. 2016;22(44):6665-6681. doi: 10.2174/1381612822666160906143249.
Medicinal inorganic chemistry plays an important role in exploring the properties of metal ions for the designing of new drugs. The field has been stimulated by the success of cis-platin, the world best selling anticancer drug and platinum complexes with reduced toxicity, oral activity and activity against resistant tumors are currently on clinical trial. The use of cis-platin is, however, severely limited by its toxic side-effects. This has stimulated chemists to employ different strategies in the development of new metal-based anticancer agents with different mechanisms of action. The discovery of new non-covalent interactions with the classical target, DNA, was the first developing step in the treatment of cancer. The use of organometallic compounds as a medicine is very common now a days because it offers potential advantages over the more common organic-based drugs. In this article we have highlighted the anticancer activity of the organotin(IV) carboxylates published in the last few years (from 2008 to 2016). In most cases they present lower IC50 values than those of cisplatin, which indicates their high activity against the cancer cell lines. The summarized data reveal that every year new organotin(IV) carboxylate complexes are synthesized with the aim of new anticancer agent with much better results than the than the corresponding activity of cis-platin or other clinically approved drugs. In addition to the advantages of high activity, compared to the platinum compound, tin complexes are much cheaper. Thus by using organotin carboxylate for clinical medicine, cost reduction, dosage reduction and effect enhancement will be reached.
药用无机化学在探索金属离子性质以设计新药方面发挥着重要作用。顺铂作为全球最畅销的抗癌药物取得成功,刺激了该领域的发展。目前,毒性降低、具有口服活性且对耐药肿瘤有活性的铂配合物正在进行临床试验。然而,顺铂的使用受到其毒副作用的严重限制。这促使化学家在开发具有不同作用机制的新型金属基抗癌药物时采用不同策略。发现与经典靶点DNA的新非共价相互作用是癌症治疗的第一步发展。如今,有机金属化合物作为药物的应用非常普遍,因为与更常见的有机药物相比,它具有潜在优势。在本文中,我们重点介绍了过去几年(2008年至2016年)发表的有机锡(IV)羧酸盐的抗癌活性。在大多数情况下,它们的半数抑制浓度(IC50)值低于顺铂,这表明它们对癌细胞系具有高活性。汇总数据显示,每年都有新的有机锡(IV)羧酸盐配合物被合成,目标是开发出比顺铂或其他临床批准药物的相应活性更好的新型抗癌药物。除了高活性的优点外,与铂化合物相比,锡配合物要便宜得多。因此,通过将有机锡羧酸盐用于临床医学,可以实现降低成本、减少剂量和增强效果。