苯并咪唑:开发抗乳腺癌新药分子的一个有希望的靶点

Balgovind Balgovind, Omprakash Goshain
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摘要

乳腺癌被认为是最致命的疾病之一,主要发生在发达国家和发展中国家。为了设计和开发更有选择性、更有效和更低毒性的更好的治疗癌症的药物,需要不断的研究。在药物化学中,融合杂环体系已被许多研究人员确定为一种特殊的结构,可以作为药物发现和开发的模板。许多具有治疗潜力的药物都含有杂芳双环体系作为药效团。根据各种文献的研究成果,取代苯并咪唑具有广泛的药理特征和多靶向能力,是设计和开发治疗乳腺癌、皮肤癌、血癌等复杂癌症的新型治疗剂的重要基础核心。在这篇文章中,我们讨论了许多科学家在过去几年的研究成果,这些成果支持苯并咪唑支架用于开发新的乳腺癌治疗药物及其作用机制。本综述还着重介绍了苯并咪唑核和乳腺癌类型的一些介绍。
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Benzimidazole: A Promising target for the development of novel drug molecules against breast cancer
Breast cancer is considered as one of the deadliest diseases dominantly in developed and developing countries. Continuous research is required in order to design and develop better therapeutic agents for cancer treatment with more selectivity, efficacy and reduced toxicity. Fused heterocyclic ring system has been identified as a privileged structure by several researchers that can be used as a template for drug discovery and development in Medicinal Chemistry. Wide range of drugs with therapeutic potential contain hetero-aromatic bicyclic ring system as pharmacophore. According to various research outputs in the literature substituted benzimidazoles have wide range of pharmacological profiles with multi-targeting ability, making them an important basic nucleus for the design and development of novel therapeutic agents for the treatment of complex cancers including breast cancer, skin cancer, and blood cancer. In the presented article we have discussed research outputs by many scientists in the last few years that support the candidature of benzimidazole scaffold for the development of novel therapeutic agents against breast cancer along with their mechanism of action. This review also focuses on little introductory idea about benzimidazole nucleus and types of breast cancer.
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