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Current Status of Some Antituberculosis Drugs and the Development of new Antituberculous Agents with Special Reference to their In Vitro and In Vivo Antimicrobial Activities

机译:一些抗结核药物的现状和新抗结核药物的开发,特别是其体外和体内抗菌活性

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Tuberculosis (TB) is a growing international health concern, since it is the leading infectious cause of death in the world today. In particular, the increasing prevalence of multidrug-resistant (MDR)-TB has greatly contributed to the increased difficulties in the control of TB. Because of the global health problems of TB, the increasing rate of MDR-TB and the high rate of a co-infection with HIV, the development of potent new anti-TB drugs without cross-resistance with known antimycobacterial agents is urgently needed. This article deals with the following areas. First, it briefly reviews some recent findings on the pharmacological status of fluoroquinolones and rifamycin derivatives. Second, it describes other types of new agents, such as oxazolidinones (linezolid, PNU-100480), nitroimidazoles (nitroimidazopyran PA-824, metronidazole), 2-pyridone, riminophenazines and diarylquinolines, which are being developed as anti-TB drugs. In addition, the future development of new antitubercular drugs is briefly discussed according to the potential pharmacological targets. New critical information on the whole genome of Mycobacterium tuberculosis (MTB) was recently elucidated and increasing knowledge on various mycobacterial virulence genes will promote the progression in the identification of genes that code for new drug targets. Using such findings on MTB genome, drug development using quantitative structureactivity relationship may be possible in the near future.
机译:结核病(TB)是国际上日益关注的健康问题,因为它是当今世界上主要的传染性死亡原因。尤其是,耐多药结核病的患病率上升,极大地增加了控制结核病的难度。由于结核病的全球性健康问题,耐多药结核病的发病率上升以及艾滋病毒的高感染率,迫切需要开发有效的新型抗结核病药物,而又不与已知的抗分枝杆菌药产生交叉耐药性。本文涉及以下领域。首先,它简要回顾了有关氟喹诺酮和利福霉素衍生物的药理状态的一些最新发现。其次,它描述了其他类型的新药,例如恶唑烷酮(利奈唑胺,PNU-100480),硝基咪唑(硝基咪唑并吡喃PA-824,甲硝唑),2-吡啶酮,吗啉吩嗪和二芳基喹啉,它们正在被开发为抗结核药物。此外,根据潜在的药理学目标简要讨论了新的抗结核药物的未来发展。最近阐明了关于结核分枝杆菌(MTB)整个基因组的新的关键信息,对各种分枝杆菌毒力基因的了解不断增加,将促进鉴定编码新药靶标的基因的进展。利用有关MTB基因组的发现,在不久的将来可能会利用定量结构活性关系开发药物。

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