New Promising Compounds with in Vitro Nanomolar Activity against Trypanosoma cruzi
摘要:
The antiparasitic activity of azole and new 4-aminopyridine derivatives has been investigated. The imidazoles 1 and 3-5 showed a potent in vitro antichagasic activity with IC50 values in the low nanomolar concentration range. The (S)-1, (S)-3, and (S)-5 enantiomers showed (up to) a thousand-fold higher activity than the reference drug benznidazole and furthermore low cytotoxicity on rat myogenic L6 cells.
New Promising Compounds with in Vitro Nanomolar Activity against <i>Trypanosoma cruzi</i>
作者:Laura Friggeri、Luigi Scipione、Roberta Costi、Marcel Kaiser、Francesca Moraca、Claudio Zamperini、Bruno Botta、Roberto Di Santo、Daniela De Vita、Reto Brun、Silvano Tortorella
DOI:10.1021/ml400039r
日期:2013.6.13
The antiparasitic activity of azole and new 4-aminopyridine derivatives has been investigated. The imidazoles 1 and 3-5 showed a potent in vitro antichagasic activity with IC50 values in the low nanomolar concentration range. The (S)-1, (S)-3, and (S)-5 enantiomers showed (up to) a thousand-fold higher activity than the reference drug benznidazole and furthermore low cytotoxicity on rat myogenic L6 cells.