以分枝杆菌MelF (Rv1936)为靶点的新型抗结核药物的设计策略

R. Dharra, Mehta Pk
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引用次数: 1

摘要

结核病(TB)是全世界的一个主要公共卫生问题。迫切需要研制新型抗结核药物(ATDs)。全细胞筛选(WCS)和基于靶标的筛选(TBS)方法被广泛用于设计新的ATDs。WCS被认为是一种相对有利的策略,但它缺乏精确的靶点知识,而基于靶点的hit化合物可能无法确保其可药物性。在本文中,我们讨论了利用TBS和虚拟配体筛选设计的针对分枝杆菌MelF (Rv1936)的强效抑制剂,并显示了与一线杀菌药物异烟肼和利福平的协同作用。
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Strategies for Designing Novel Anti-Tubercular Drugs with Special Reference to Mycobacterial MelF (Rv1936) as a Target
Tuberculosis (TB) is a major public health problem throughout the world. There is an immediate need to device novel anti-tubercular drugs (ATDs). Whole cell screening (WCS) and target based screening (TBS) approaches are widely used to devise new ATDs. WCS is considered relatively a favourable strategy but it lacks in the precise target knowledge, whereas the target based hit compounds may not ensure the drugability. In this manuscript, we have discussed the potent inhibitors designed against the mycobacterial MelF (Rv1936) by using the TBS as well as virtual ligand screening, which also revealed synergistic effect with the first-line bactericidal drugs, i.e., isoniazid and rifampicin.
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