¡Nos trasladamos! E-Prints cerrará el 7 de junio.

En las próximas semanas vamos a migrar nuestro repositorio a una nueva plataforma con muchas funcionalidades nuevas. En esta migración las fechas clave del proceso son las siguientes:

Es muy importante que cualquier depósito se realice en E-Prints Complutense antes del 7 de junio. En caso de urgencia para realizar un depósito, se puede comunicar a docta@ucm.es.

In Vitro Primary Screening of a Synthetic Series of Chromenoazoldiones against Trypanosoma cruzi



Downloads per month over past year

Fonseca Berzal, Cristina Rosa and Morales, Paula and Escario Garcia-Trevijano, José Antonio and Gómez Barrio, Alicia and Jagerovic, Nadine (2017) In Vitro Primary Screening of a Synthetic Series of Chromenoazoldiones against Trypanosoma cruzi. Proceedings, 1 (6). p. 650. ISSN 2504-3900

[thumbnail of Abstract]
PDF (Abstract)
Creative Commons Attribution.


Official URL: https://doi.org/10.3390/proceedings1060650


Similarities between parasites and cancer have prompted parasitologists to take advantage of several approaches enabled by cancer research to identify antiparasitic agents [1]. Quinones generate reactive oxygen species (ROS), which not only results in their antitumor properties, but also in a mechanism for designing antichagasic drugs. Here, a synthetic series of seven chromenoazoldiones previously defined as potential antitumorals [2,3], has been assayed in vitro against Trypanosoma cruzi (CL-B5 lacZ strain) in a primary screening that evaluates activity over epimastigotes and toxicity on L929 cells [4,5]. Compounds PM199, PM203 and PM401 achieved higher IC50 values than that of the reference drug benznidazole (BZ): IC50 = 14.45 ± 1.90, 14.84 ± 4.49, 16.01 ± 9.06 and 36.47 ± 4.43 µM (PM199, PM203, PM401 and BZ, respectively). However, their higher cytotoxicity led to a lower selectivity (SI) on epimastigotes: SIPM199 = 5.83, SIPM203 = 7.03, SIPM401 = 5.27 and SIBZ > 7.02. Only two compounds showed no cytotoxicity (LC50 > 256 µM) and thus, no derivative was further assayed against intracellular amastigotes. These chromenoazoldiones did not show relevant activity on T. cruzi. Their cytotoxicity, probably connected to ROS production in mammalian cells, encourages further optimization to apply them as trypanocidal templates.

Item Type:Article
Subjects:Medical sciences > Pharmacy > Microbiology
ID Code:68754
Deposited On:11 Feb 2022 12:31
Last Modified:11 Feb 2022 13:05

Origin of downloads

Repository Staff Only: item control page