3-halo chloroquine derivatives overcome Plasmodium falciparum chloroquine resistance transporter-mediated drug resistance in P. falciparum

8Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Polymorphism in the Plasmodium falciparum chloroquine resistance transporter (PfCRT) was shown to cause chloroquine resistance. In this report, we examined the antimalarial potential of novel 3-halo chloroquine derivatives (3-chloro, 3-bromo, and 3-iodo) against chloroquine-susceptible and -resistant P. falciparum. All three derivatives inhibited the proliferation of P. falciparum; with 3-iodo chloroquine being most effective. Moreover, 3-iodo chloroquine was highly effective at potentiating and reversing chloroquine toxicity of drug-susceptible and -resistant P. falciparum.

Cite

CITATION STYLE

APA

Edaye, S., Tazoo, D., Bohle, D. S., & Georges, E. (2015). 3-halo chloroquine derivatives overcome Plasmodium falciparum chloroquine resistance transporter-mediated drug resistance in P. falciparum. Antimicrobial Agents and Chemotherapy, 59(12), 7891–7893. https://doi.org/10.1128/AAC.01139-15

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free