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Computer-Aided Drug Design Using Sesquiterpene Lactones as Sources of New Structures with Potential Activity against Infectious Neglected Diseases

机译:使用倍半萜内酯作为新结构的来源的计算机辅助药物设计该结构具有针对传染性被忽视疾病的潜在活性

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摘要

This review presents an survey to the biological importance of sesquiterpene lactones (SLs) in the fight against four infectious neglected tropical diseases (NTDs)—leishmaniasis, schistosomiasis, Chagas disease, and sleeping sickness—as alternatives to the current chemotherapies that display several problems such as low effectiveness, resistance, and high toxicity. Several studies have demonstrated the great potential of some SLs as therapeutic agents for these NTDs and the relationship between the protozoal activities with their chemical structure. Recently, Computer-Aided Drug Design (CADD) studies have helped increase the knowledge of SLs regarding their mechanisms, the discovery of new lead molecules, the identification of pharmacophore groups and increase the biological activity by employing in silico tools such as molecular docking, virtual screening and Quantitative-Structure Activity Relationship (QSAR) studies.
机译:这篇综述对倍半萜内酯(SLs)在对抗四种传染性被忽视的热带疾病(利什曼病,血吸虫病,恰加斯病和昏睡病)中的生物学重要性进行了一项调查,作为替代目前存在一些问题的化学疗法的化学疗法具有低效,抗药性和高毒性的特点。几项研究表明,某些SL可以作为这些NTD的治疗剂,并且具有原生动物活性与其化学结构之间的关系。最近,计算机辅助药物设计(CADD)研究已通过使用计算机模拟工具(例如分子对接,虚拟)来提高SL对它们的机理,新的前导分子的发现,药效基团基团的识别以及增加生物活性的认识。筛选和定量结构活动关系(QSAR)研究。

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