Liñares Guadalupe García, Gismondi Santiago, Codesido Nicolás Osa, Moreno Silvia N J, Docampo Roberto, Rodriguez Juan B
Departamento de Química Orgánica and UMYMFOR (CONICET-FCEyN), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón 2, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina.
Bioorg Med Chem Lett. 2007 Sep 15;17(18):5068-71. doi: 10.1016/j.bmcl.2007.07.012. Epub 2007 Jul 13.
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 threefold more potent than our lead drug 1 against intracellular T. cruzi. The biological evaluation against T. gondii was also very promising. The IC(50) values corresponding to 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.
作为我们旨在开发针对热带疾病的新型安全化疗和化学预防药物项目的一部分,设计、合成了与4-苯氧基苯氧基乙基硫氰酸盐(1)结构相关的含氟药物,并评估了其作为抗增殖剂对克氏锥虫(美洲锥虫病,即恰加斯病的病原体)及刚地弓形虫(弓形虫病的病原体)的作用。此前已证明该硫氰酸盐衍生物是一种有效的抗克氏锥虫增殖药物。含氟硫氰酸盐衍生物2和3对细胞内克氏锥虫的效力比我们的先导药物1高三倍。针对刚地弓形虫的生物学评估也很有前景。化合物2和3对刚地弓形虫速殖子的半数抑制浓度(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,不仅作为先导药物具有突出潜力,而且还可用于进一步的体内研究。