Recent Progress in the Development of Novel Mycobacterium Cell Wall Inhibitor to Combat Drug-Resistant Tuberculosis

T. M. Belete
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引用次数: 4

Abstract

Despite decades of research in drug development against TB, it is still the leading cause of death due to infectious diseases. The long treatment duration, patient noncompliance coupled with the ability of the tuberculosis bacilli to resist the current drugs increases multidrug-resistant tuberculosis that exacerbates the situation. Identification of novel drug targets is important for the advancement of drug development against Mycobacterium tuberculosis. The development of an effective treatment course that could help us eradicates TB. Hence, we require drugs that could eliminate the bacteria and shorten the treatment duration. This review briefly describes the available data on the peptidoglycan component structural characterization, identification of the metabolic pathway, and the key enzymes involved in the peptidoglycan synthesis, like N-Acetylglucosamine-1-phosphate uridyltransferase, mur enzyme, alanine racemase as well as their inhibition. Besides, this paper also provides studies on mycolic acid and arabinogalactan synthesis and the transport mechanisms that show considerable promise as new targets to develop a new product with their inhibiter.
新型抗结核分枝杆菌细胞壁抑制剂的研究进展
尽管在结核病药物开发方面进行了几十年的研究,但它仍然是导致传染病死亡的主要原因。治疗时间长,患者不依从,再加上结核杆菌对现有药物的抵抗能力,增加了耐多药结核病,从而加剧了这种情况。确定新的药物靶点对于促进抗结核分枝杆菌的药物开发具有重要意义。制定一个有效的治疗方案,帮助我们根除结核病。因此,我们需要能够消除细菌并缩短治疗时间的药物。本文简要介绍了肽聚糖组分的结构表征、代谢途径的鉴定以及参与肽聚糖合成的关键酶,如N-乙酰葡糖胺-1-磷酸尿苷基转移酶、mur酶、丙氨酸外消旋酶及其抑制作用的现有数据。此外,本文还对分枝杆菌酸和阿拉伯半乳聚糖的合成及其转运机制进行了研究,这些研究显示出相当大的前景,可以作为开发其抑制剂新产品的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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