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结核分枝杆菌DprE1抑制剂——Macozinone
Mycobacterium tuberculosis DprE1 inhibitor——Macozinone
【摘要】 结核病(TB),尤其是耐多药TB(MDR-TB)是近20年全球细菌感染引起死亡的第一杀手,故寻找具有全新作用机制的抗TB新药迫在眉睫。Macozinone(研发代号:PBTZ169)是靶向于DprE1的新型抗MDR-TB候选药物,通过抑制结核分枝杆菌细胞壁的合成发挥杀菌作用,目前处于Ⅱ期临床研究阶段。本文就Macozinone的基本信息、作用机制、临床前研究及临床研究等方面作一概述。
【Abstract】 Tuberculosis(TB),especially multidrug-resistant TB(MDR-TB),is the leading cause of death from bacterial infections in the past 20 years globally. Thus,there is an urgent need to develop new anti-TB drugs with novel mechanism.Macozinone(development code:PBTZ169),a new anti-MDR-TB candidate targeting DprE1,exerts bactericidal effect through inhibiting the synthesis of Mycobacterial tuberculosis cell wall,is currently being tested in phase Ⅱ clinical trial. Basic information,mechanism of action,pre-clinical and clinical research of Macozinone were summarized in this review.
【Key words】 Macozinone; PBTZ169; tuberculosis; DprE1 inhibitor;
- 【文献出处】 临床药物治疗杂志 ,Clinical Medication Journal , 编辑部邮箱 ,2022年04期
- 【分类号】R978.3
- 【下载频次】56