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Fluorine-containing aryloxyethyl thiocyanate derivatives are potent inhibitors of Trypanosoma cruzi and Toxoplasma gondii proliferation

机译:含氟芳氧基乙基硫氰酸酯衍生物是克鲁斯锥虫和弓形虫增殖的有效抑制剂

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摘要

As a part of our project aimed at developing new safe chemotherapeutic and chemoprophylactic agents against tropical diseases, fluorine-containing drugs structurally related to 4-phenoxyphenoxyethyl thiocyanate (>1) were designed, synthesized and evaluated as antiproliferative agents against Trypanosoma cruzi, the parasite responsible of American trypanosomiasis (Chagas’ disease) and Toxoplasma gondii, the etiological agent of toxoplasmosis. This thiocyanate derivative had previously proven to be an effective agent against T. cruzi proliferation. Fluorine-containing thiocyanate derivatives >2 and >3 were 3-fold more potent than our lead drug >1 against intracellular T. cruzi. The biological evaluation against T. gondii was also very promising. The IC50 values corresponding for >2 and >3 were at the very low micromolar level against tachyzoites of T. gondii. Both of these drugs are interesting examples of effective antiparasitic agents that have outstanding potential not only as lead drugs but also to be used for further in vivo studies.
机译:作为我们旨在开发针对热带疾病的新型安全化学疗法和化学预防剂的项目的一部分,设计,合成并评估了与4-苯氧基苯氧基乙基硫氰酸酯(> 1 )结构相关的含氟药物,作为针对此类疾病的抗增殖药克氏锥虫,寄生于美国锥虫病(恰加斯氏病)和弓形虫,弓形虫病的病原体。先前已证明该硫氰酸酯衍生物是对抗克鲁氏锥虫增殖的有效试剂。含氟的硫氰酸盐衍生物> 2 和> 3 对细胞内克鲁氏杆菌的功效比我们的先导药物> 1 高3倍。对弓形虫的生物学评估也非常有前途。针对刚地弓形虫速殖子的> 2 和> 3 的IC50值处于非常低的微摩尔水平。这两种药物都是有效的抗寄生虫药物的有趣实例,它们不仅具有作为先导药物的突出潜力,而且还可以用于进一步的体内研究。

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