Upegui Yulieth, Gil Juan F, Quiñones Wiston, Torres Fernando, Escobar Gustavo, Robledo Sara M, Echeverri Fernando
PECET, Instituto de Investigaciones Médicas, Facultad de Medicina, Universidad de Antioquia, Calle 70 #52-21, Medellín 050010, Colombia.
Grupo Química Orgánica de Productos Naturales, Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Calle 70 #52-21, Medellín 050010, Colombia.
Molecules. 2014 Nov 18;19(11):18911-22. doi: 10.3390/molecules191118911.
Six derivatives of the known biopesticide rotenone were prepared by several chemical transformations. Rotenone and its derivatives showed differential in vitro antiparasitic activity and selective cytotoxicity. In general, compounds were more active against Plasmodium falciparum than Leishmania panamensis. Rotenone had an EC50 of 19.0 µM against P. falciparum, and 127.2 µM against L. panamensis. Although chemical transformation does not improve its biological profile against P. falciparum, three of its derivatives showed a significant level of action within an adequate range of activity with EC50 values < 50.0 µM. This antiplasmodial activity was not due to red blood cell hemolysis, since LC50 was >>400 µM. On the other hand, all derivatives displayed a non-specific cytotoxicity on several cell lines and primary human cell cultures.
通过几种化学转化方法制备了已知生物农药鱼藤酮的六种衍生物。鱼藤酮及其衍生物表现出不同的体外抗寄生虫活性和选择性细胞毒性。一般来说,化合物对恶性疟原虫的活性比对巴拿马利什曼原虫更强。鱼藤酮对恶性疟原虫的EC50为19.0μM,对巴拿马利什曼原虫的EC50为127.2μM。虽然化学转化并未改善其对恶性疟原虫的生物学特性,但其中三种衍生物在EC50值<50.0μM的适当活性范围内表现出显著的作用水平。这种抗疟活性不是由于红细胞溶血,因为LC50>>400μM。另一方面,所有衍生物对几种细胞系和原代人细胞培养物均表现出非特异性细胞毒性。