Drug Design & Medicinal Chemistry Lab, Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research , New Delhi , India.
Regulatory Affairs Division, Genpact India Pvt Ltd , Mumbai , India.
Expert Opin Ther Pat. 2019 Sep;29(9):703-731. doi: 10.1080/13543776.2019.1651841. Epub 2019 Aug 8.
: Combretastatins represent a potent class of phenolic-stilbene natural products that function as colchicine binding site inhibitors of tubulin polymerization and have been advanced as promising anticancer lead compounds. Among them, combretastatin A-4 is the most potent lead molecule due to its broad spectrum cytotoxicity against a variety of tumors. However, low water solubility due to its high lipophilic nature and inter-conversion of olefinic double bond from more active to less active conformation poses limitations to its clinical utility. However, different approaches including prodrugs, salt formations, structural modifications, prevention of inter-conversion of the olefinic bond and changes to the substitution pattern on the rings of combretastatin A-4 were investigated and successfully resulted in different combretastatin-based molecules that demonstrated varying levels of potency against different types of tumors during their and studies. : This review covers the patents over a period of 2008-2018. : Molecular hybridization and prodrug designing imparted multi-targeted actions to combretastatin derivatives. Currently, various combretastatin derivatives are under clinical trials. These derivatives could be used to treat disorders other than cancer, due to their vascular disrupting action.
: 紫檀芪类化合物是一类具有酚类-查耳酮结构的天然产物,作为微管蛋白聚合抑制剂,能与秋水仙碱结合,已被作为很有前途的抗癌先导化合物进行研究。其中,由于对多种肿瘤具有广谱细胞毒性,紫檀芪 A-4 是最有效的先导分子。然而,由于其高亲脂性,导致其水溶性低,并且由于双键的顺反异构,从更活跃的构象转化为不活跃的构象,限制了其临床应用。然而,已经研究了不同的方法,包括前药、盐形成、结构修饰、防止双键的互变以及改变紫檀芪 A-4 环上的取代模式,这些方法成功地得到了不同的基于紫檀芪的分子,在临床前和临床研究中对不同类型的肿瘤表现出不同程度的活性。 : 本文综述了 2008 年至 2018 年期间的专利。 : 分子杂交和前药设计赋予了紫檀芪衍生物多靶点作用。目前,各种紫檀芪衍生物正在进行临床试验。由于其血管破坏作用,这些衍生物可用于治疗除癌症以外的疾病。