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具有治疗特性的基于 Combretastatin 的化合物:专利审查。

Combretastatin-based compounds with therapeutic characteristics: a patent review.

机构信息

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.

出版信息

Expert Opin Ther Pat. 2019 Sep;29(9):703-731. doi: 10.1080/13543776.2019.1651841. Epub 2019 Aug 8.

Abstract

: 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.

摘要

: 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。

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