Recent Developments of Target-Based Benzimidazole Derivatives as Potential Anticancer Agents

N. S. Goud, Pardeep Kumar, R. Bharath
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引用次数: 11

Abstract

Cancer is one of the major life burdens and around 18.1 million new cancer cases and 9.6 million deaths have been estimated in 2018 globally. Recent reports of the World Health Organization (WHO) stated that about one in six death cases globally is mainly due to cancer. Hence, the development of efficacious drugs with novel mechanisms is necessary for various cancer types. The chemotherapy drug resistance and non-selectivity toward targets have turned the current cancer research on to the highly emerging selective targets for the development of potential anticancer agents. Benzimidazole is regarded as an essential pharmacophore of the cancer research because of wide anticancer potentials with versatile mechanisms to inhibit the tumor progression and also facile synthetic strategies for an easy synthesis of various benzimidazole derivatives. The selective anticancer potentials also depend on the substitution of the benzimidazole nucleus. Therefore, it would lead to providing a path for the development of novel target-specific and highly effective benzimidazole-based anticancer agents.
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癌症是主要的生活负担之一,据估计,2018年全球约有1810万新发癌症病例和960万例死亡。世界卫生组织(世卫组织)最近的报告指出,全球大约六分之一的死亡病例主要是癌症造成的。因此,开发具有新机制的有效药物对于不同类型的癌症是必要的。化疗药物的耐药和对靶点的非选择性使当前的癌症研究转向高度新兴的选择性靶点,以开发潜在的抗癌药物。苯并咪唑具有广泛的抗癌潜力和多种抑制肿瘤进展的机制,并且易于合成各种苯并咪唑衍生物,因此被认为是癌症研究中必不可少的药效团。选择性抗癌潜能也依赖于苯并咪唑核的取代。因此,这将为开发新的靶向性和高效的苯并咪唑类抗癌药物提供一条途径。
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