Leal Sandra M, Amado Diego F, Kouznetsov Vladimir V, Escobar Patricia
Centro de Investigación de Enfermedades Tropicales, CINTROP, Departamento de Ciencias Básicas, Escuela de Medicina, Universidad Industrial de Santander, Bucaramanga, Colombia.
Sci Pharm. 2013 Jan-Mar;81(1):43-55. doi: 10.3797/scipharm.1205-14. Epub 2012 Oct 14.
The leishmaniasis and Chagas diseases constitute a serious public health problem worldwide with few and ineffective treatment options. The search for new antiparasitic candidates at the initial steps of drug discovery and development is still necessary. The synthesis of 22 de novo synthetized N,N'-dihetaryl-alkyldiamine derivatives and in vitro antiparasitic activity were evaluated for the first time against intracellular and extracellular forms of Leishmania (Leishmania) infantum, L. (Viannia) panamensis, L. (Leishmania) amazonensis, and Trypanosoma cruzi. Additionally, the toxicity on mammalian cells was determined. Some of these substituted N,N'-diamines (25-35 % of the tested compounds) showed interesting results against free-living forms of parasites with activities at the inhibitory concentration (IC 50 ) level of 1.96 to 28.83 μM for L. (L.) infantum promastigotes and IC50 of 0.02 to 5.31 μM for T. cruzi epimastigotes. No activity at the IC50 level on intracellular amastigotes of T. cruzi was observed. However, N (1),N (2)-dibenzylethane-1,2-diamine 5a revealed an important activity against the intracellular amastigotes of L. infantum (IC50 25.42 μM ±0.33) and L. panamensis (IC50 58.20 μM ±3.23), while their analogue N(1),N(4) -dibenzylbutane-1,4-diamine 5c resulted in activity only against L. panamensis (IC50 11.19 μM ±0.20) without toxicity on Vero and THP-1 mammalian cells. The active compounds against intracellular parasites with low toxicity in mammalian cells may be considered for future studies in experimental models.
利什曼病和恰加斯病在全球范围内构成严重的公共卫生问题,治疗选择极少且效果不佳。在药物研发的初始阶段寻找新的抗寄生虫候选药物仍然很有必要。首次评估了22种从头合成的N,N'-二杂芳基烷基二胺衍生物的合成及其对婴儿利什曼原虫(利什曼原虫属)、巴拿马利什曼原虫(维安尼亚利什曼原虫属)、亚马逊利什曼原虫(利什曼原虫属)和克氏锥虫细胞内和细胞外形式的体外抗寄生虫活性。此外,还测定了其对哺乳动物细胞的毒性。其中一些取代的N,N'-二胺(占测试化合物的25 - 35%)对游离寄生虫形式显示出有趣的结果,对婴儿利什曼原虫前鞭毛体的抑制浓度(IC50)水平为1.96至28.83 μM,对克氏锥虫上鞭毛体的IC50为0.02至5.31 μM。未观察到对克氏锥虫细胞内无鞭毛体的IC50水平活性。然而,N(1),N(2)-二苄基乙烷-1,2-二胺5a对婴儿利什曼原虫(IC50 25.42 μM ±0.33)和巴拿马利什曼原虫(IC50 58.20 μM ±3.23)的细胞内无鞭毛体显示出重要活性,而其类似物N(1),N(4)-二苄基丁烷-1,4-二胺5c仅对巴拿马利什曼原虫有活性(IC50 11.19 μM ±0.20),对Vero和THP-1哺乳动物细胞无毒性。对细胞内寄生虫有活性且在哺乳动物细胞中低毒性的活性化合物可考虑用于未来实验模型的研究。