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DRUG DISCOVERY IN TUBERCULOSIS: A MOLECULAR APPROACH

机译:结核病的药物发现:一种分子方法

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摘要

Despite unquestionable success of the combination drug therapy, tuberculosis (TB) very recently has drawn major attention because of the global upsurge of MDR-TB, XDR -TB and HTV-TB co-infection cases. In the last four decades, only one compound is added to the treatment regimen leaving ample opportunities to find out a new generation of TB drugs. The modern concept of drug discovery utilizes the integrated knowledge of genomics, proteomics, molecular biology and systems biology to identify more specific targets. The purpose of this review is to revisit the field of tuberculosis drug discovery based on those new concepts to identify novel targets.
机译:尽管联合药物疗法取得了毫无疑问的成功,但由于全球耐多药结核病,广泛耐药结核病和结核分枝杆菌感染的病例激增,结核病(TB)最近引起了人们的广泛关注。在过去的四十年中,仅将一种化合物添加到治疗方案中,这为寻找新一代结核病药物提供了充足的机会。现代药物发现概念利用基因组学,蛋白质组学,分子生物学和系统生物学的综合知识来识别更具体的靶标。这篇综述的目的是基于那些新概念来重新鉴定结核病药物发现领域,以发现新的靶标。

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