Department of Pharmacy, University of Genoa, viale Benedetto XV n.3, Genoa 16132, Italy.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, via Aldo Moro 2, Siena 53100, Italy.
ACS Infect Dis. 2024 Aug 9;10(8):2755-2774. doi: 10.1021/acsinfecdis.4c00113. Epub 2024 Jul 2.
Folate enzymes, namely, dihydrofolate reductase (DHFR) and pteridine reductase (PTR1) are acknowledged targets for the development of antiparasitic agents against Trypanosomiasis and Leishmaniasis. Based on the amino dihydrotriazine motif of the drug Cycloguanil (Cyc), a known inhibitor of both folate enzymes, we have identified two novel series of inhibitors, the 2-amino triazino benzimidazoles () and 2-guanidino benzimidazoles (), as their open ring analogues. Enzymatic screening was carried out against PTR1, DHFR, and thymidylate synthase (TS). The crystal structures of DHFR and PTR1 in complex with selected compounds experienced in both cases a substrate-like binding mode and allowed the rationalization of the main chemical features supporting the inhibitor ability to target folate enzymes. Biological evaluation of both series was performed against and and the toxicity against THP-1 human macrophages. Notably, the 5,6-dimethyl-2-guanidinobenzimidazole resulted to be the most potent ( = 9 nM) and highly selective DHFR inhibitor, 6000-fold over PTR1 and 394-fold over DHFR. The 5,6-dimethyl tricyclic analogue , despite showing a lower potency and selectivity profile than , shared a comparable antiparasitic activity against in the low micromolar domain. The dichloro-substituted 2-guanidino benzimidazoles and revealed their potent and broad-spectrum antitrypanosomatid activity affecting the growth of and parasites. Therefore, both chemotypes could represent promising templates that could be valorized for further drug development.
叶酸酶,即二氢叶酸还原酶(DHFR)和喋呤还原酶(PTR1),是开发用于对抗锥虫病和利什曼病的抗寄生虫药物的公认靶标。基于药物环胍(Cyc)的氨基酸二氢三嗪基序,它是两种叶酸酶的已知抑制剂,我们已经确定了两个新的抑制剂系列,即 2-氨基三嗪苯并咪唑()和 2-胍基苯并咪唑(),作为它们的开环类似物。对 PTR1、DHFR 和胸苷酸合酶(TS)进行了酶筛选。DHFR 和 PTR1 与所选化合物的晶体结构在两种情况下都经历了类似底物的结合模式,并允许合理化支持抑制剂靶向叶酸酶能力的主要化学特征。对这两个系列进行了针对和的生物评估,并对 THP-1 人巨噬细胞的毒性进行了评估。值得注意的是,5,6-二甲基-2-胍基苯并咪唑是最有效的(=9 nM)和高度选择性的 DHFR 抑制剂,对 PTR1 的抑制活性比 DHFR 高 6000 倍。尽管 5,6-二甲基三环类似物的效力和选择性谱比低,但与相比,它具有相似的抗寄生虫活性,在低微摩尔范围内对具有活性。二氯取代的 2-胍基苯并咪唑和表现出强大而广谱的抗锥虫原虫活性,影响和寄生虫的生长。因此,这两种化学类型都可能代表有前途的模板,可以进一步开发药物。