...
首页> 外文期刊>Expert opinion on therapeutic targets >Type-II NADH Dehydrogenase (NDH-2): a promising therapeutic target for antitubercular and antibacterial drug discovery
【24h】

Type-II NADH Dehydrogenase (NDH-2): a promising therapeutic target for antitubercular and antibacterial drug discovery

机译:II型NADH脱氢酶(NDH-2):对抗细胞和抗菌药物发现的有前途的治疗靶标

获取原文
获取原文并翻译 | 示例
           

摘要

Introduction: Tuberculosis (TB) is highly dangerous due to the development of resistance to first-line drugs. Moreover, Mycobacterium tuberculosis (Mtb) has also developed resistance to newly approved antitubercular drug bedaquiline. This necessitates the search for drugs acting on newer molecular targets. The energy metabolism of mycobacteria is the prime focus for the discovery of novel antitubercular drugs. Targeting type-2 NADH dehydrogenase (NDH-2) involved in the production of respiratory ATP could, therefore, be effective in treating the disease.Areas covered: This review describes the energetics of mycobacteria and the role of NDH-2 in ATP synthesis. Special attention has been given for genetic and chemical validations of NDH-2 as a molecular target. The reported kinetics and crystal structures of NDH-2 have been given in detail for better understanding of the enzyme.Expert opinion: NDH-2 is an essential enzyme for ATP synthesis and has a potential role in dormancy and persistence of Mtb. The human counterpart lacks this enzyme and hence NDH-2 inhibitors could have more clinical importance. Phenothiazines are potent inhibitor of NDH-2 and are effective against both drug-susceptible and drug-resistant Mtb. Thus, it is highly desirable to optimize phenothiazine class of compounds for the development of next generation anti-TB drugs.
机译:简介:由于对一线药物的耐药性,结核病(TB)非常危险。此外,结核分枝杆菌(MTB)也对新批准的抗细胞药物Bedaquiline产生了抗性。这需要寻求作用于新分子靶标的药物。分枝杆菌的能量代谢是对新型抗细胞药物发现的主要重点。因此,涉及呼吸道ATP的产生的2型NADH脱氢酶(NDH-2)可以有效治疗疾病。覆盖:本综述描述了分枝杆菌的能量和NDH-2在ATP合成中的作用。已经特别注意NDH-2作为分子靶标的遗传和化学验证。已经详细给出了NDH-2的报告的动力学和晶体结构,以便更好地了解酶意见:NDH-2是ATP合成的必要酶,并且在MTB的休眠和持续存在下具有潜在作用。人体对应物缺乏这种酶,因此NDH-2抑制剂可具有更高的临床重要性。吩噻嗪是NDH-2的有效抑制剂,对药物易受和耐药MTB有效。因此,非常希望优化吩噻嗪类化合物以用于开发下一代抗结核药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号