Department of Parasitology, Instituto de Investigación Biosanitaria (ibs.Granada), Hospitales Universitarios de Granada, University of Granada, c/ Severo Ochoa s/n, 18071, Granada, Spain.
Department of Inorganic and Analytical Chemistry, Faculty of Chemical and Pharmaceutical Sciences, University of Chile, Box 233, Santiago, 8380492, Chile.
ChemMedChem. 2018 Oct 8;13(19):2104-2118. doi: 10.1002/cmdc.201800512. Epub 2018 Sep 4.
Chagas disease, a neglected tropical disease caused by infection with the protozoan parasite Trypanosoma cruzi, is a potentially life-threatening illness that affects 5-8 million people in Latin America, and more than 10 million people worldwide. It is characterized by an acute phase, which is partly resolved by the immune system, but then develops as a chronic disease without an effective treatment. There is an urgent need for new antiprotozoal agents, as the current standard therapeutic options based on benznidazole and nifurtimox are characterized by limited efficacy, toxicity, and frequent failures in treatment. In vitro and in vivo assays were used to identify some new low-cost 5-nitroindazoles as a potential antichagasic therapeutic alternative. Compound 16 (3-benzyloxy-5-nitro-1-vinyl-1H-indazole) showed improved efficiency and lower toxicity than benznidazole in both in vitro and in vivo experiments, and its trypanocidal activity seems to be related to its effect at the mitochondrial level. Therefore, compound 16 is a promising candidate for the development of a new anti-Chagas agent, and further preclinical evaluation should be considered.
恰加斯病,一种由原生动物寄生虫克氏锥虫感染引起的被忽视的热带病,是一种潜在的危及生命的疾病,影响拉丁美洲的 500 万至 800 万人,以及全球超过 1000 万人。它的特征是急性期,部分由免疫系统解决,但随后发展为慢性疾病,没有有效的治疗方法。迫切需要新的抗原生动物药物,因为目前基于苯并咪唑和硝呋替莫的标准治疗选择具有疗效有限、毒性和治疗频繁失败的特点。体外和体内试验用于鉴定一些新的低成本 5-硝基吲唑作为潜在的抗恰加斯病治疗替代物。化合物 16(3-苄氧基-5-硝基-1-乙烯基-1H-吲唑)在体外和体内实验中均显示出比苯并咪唑更高的效率和更低的毒性,其杀锥虫活性似乎与其在线粒体水平的作用有关。因此,化合物 16 是开发新型抗恰加斯病药物的有希望的候选物,应考虑进一步进行临床前评估。