An overview on target-based drug design against kinetoplastid protozoan infections: Human african trypanosomiasis, chagas disease and leishmaniases

82Citations
Citations of this article
146Readers
Mendeley users who have this article in their library.

Abstract

The protozoan diseases Human African Trypanosomiasis (HAT), Chagas disease (CD), and leishmaniases span worldwide and therefore their impact is a universal concern. The present regimen against kinetoplastid protozoan infections is poor and insufficient. Target-based design expands the horizon of drug design and development and offers novel chemical entities and potential drug candidates to the therapeutic arsenal against the aforementioned neglected diseases. In this review, we report the most promising targets of the main kinetoplastid parasites, as well as their corresponding inhibitors. This overview is part of the Special Issue, entitled “Advances of Medicinal Chemistry against Kinetoplastid Protozoa (Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp.) Infections: Drug Design, Synthesis and Pharmacology”.

Cite

CITATION STYLE

APA

Kourbeli, V., Chontzopoulou, E., Moschovou, K., Pavlos, D., Mavromoustakos, T., & Papanastasiou, I. P. (2021, August 1). An overview on target-based drug design against kinetoplastid protozoan infections: Human african trypanosomiasis, chagas disease and leishmaniases. Molecules. MDPI AG. https://doi.org/10.3390/molecules26154629

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