Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Curr Med Chem. 2019;26(23):4454-4475. doi: 10.2174/0929867325666180426164352.
Interest in nitroheterocyclic drugs for the treatment of infectious diseases has undergone a resurgence in recent years. Here we review the current status of monocyclic and bicyclic nitroheterocyclic compounds as existing or potential new treatments for visceral leishmaniasis, Chagas' disease and human African trypanosomiasis. Both monocyclic (nifurtimox, benznidazole and fexinidazole) and bicyclic (pretomanid (PA-824) and delamanid (OPC-67683)) nitro-compounds are prodrugs, requiring enzymatic activation to exert their parasite toxicity. Current understanding of the nitroreductases involved in activation and possible mechanisms by which parasites develop resistance is discussed along with a description of the pharmacokinetic / pharmacodynamic behaviour and chemical structure-activity relationships of drugs and experimental compounds.
近年来,人们对用于治疗传染病的硝基杂环药物重新产生了兴趣。在这里,我们综述了单环和双环硝基杂环化合物作为现有或潜在的新疗法,用于治疗内脏利什曼病、恰加斯病和非洲人类锥虫病。单环(硝呋替莫、苯并硝唑和非昔硝唑)和双环(普雷托马尼德(PA-824)和德拉马尼德(OPC-67683))硝基化合物都是前药,需要酶激活来发挥其寄生虫毒性。本文讨论了参与激活的硝基还原酶,以及寄生虫产生耐药性的可能机制,还描述了药物和实验化合物的药代动力学/药效学行为和化学结构-活性关系。