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Identification of a New Amide-Containing Thiazole as a Drug Candidate for Treatment of Chagas' Disease

机译:确定一种新的含酰胺的噻唑类药物来治疗南美锥虫病

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摘要

Although the parasitic infection Chagas' disease was described over 100 years ago, even now there are not suitable drugs. The available drugs nifurtimox and benznidazole have limited efficacies and tolerances, with proven mutagenic effects. Attempting to find appropriate drugs to deal with this problem, here we report on the development and pharmacological characterization of new amide-containing thiazoles. In the present study, we evaluated the in vitro and in vivo effects of new candidates against Trypanosoma cruzi, the etiological agent of Chagas' disease. The lead amide-containing thiazole derivative had potent in vitro activity, an absence of both in vitro mutagenic and in vivo clastogenic effects, and excellent in vitro selectivity and in vivo tolerance. The compound suppressed parasitemia in mice, modifying the anti-T. cruzi antibodies like the reference drug, benznidazole, and displayed the lowest mortality among the tested drugs. The present evidence suggests that this compound is a promising anti-T. cruzi agent surpassing the lead optimization stage in drug development and leading to a candidate for preclinical study.
机译:尽管寄生虫感染恰加斯氏病已有100多年的历史,但即使到现在,也没有合适的药物。可用的药物硝呋替莫克斯和苯硝唑具有有限的功效和耐受性,并具有诱变作用。为了找到合适的药物来解决这个问题,我们在这里报告了新的含酰胺噻唑的开发和药理特性。在本研究中,我们评估了新候选药物对抗恰加斯氏病的病原体克氏锥虫的体外和体内作用。含铅酰胺的噻唑衍生物具有有效的体外活性,不具有体外诱变和体内产生胶束的作用,并且具有出色的体外选择性和体内耐受性。该化合物抑制了小鼠体内的寄生虫病,从而改变了抗T抗体。 Cruzi抗体,例如参比药物,苯并咪唑,在被测药物中显示出最低的死亡率。目前的证据表明该化合物是有前途的抗T。 Cruzi试剂已超过药物开发的领先优化阶段,并有望成为临床前研究的候选药物。

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