Recent Advances in the Development of Broad-Spectrum Antiprotozoal Agents.

Curr Med Chem

Laboratorio de Biotecnologia Farmaceutica, Centro de Biotecnologia Genomica, Instituto Politecnico Nacional, Reynosa 88710, Mexico.

Published: February 2021

AI Article Synopsis

  • Infections from protozoa like Trypanosoma brucei and Plasmodium spp. contribute to over 500 million cases annually, impacting both rich and poor countries.
  • Current treatments are limited, highlighting the need for new drugs in development to enhance therapies for these parasitic infections.
  • The review explores various heterocyclic compounds, such as diamidine and quinoline, that may serve as promising antiprotozoal agents for future pharmacological advancements.

Article Abstract

Infections caused by Trypanosoma brucei, Trypanosoma cruzi, Leishmania spp., Entamoeba histolytica, Giardia lamblia, Plasmodium spp., and Trichomonas vaginalis, are part of a large list of human parasitic diseases. Together, they cause more than 500 million infections per year. These protozoa parasites affect both low- and high-income countries and their pharmacological treatments are limited. Therefore, new and more effective drugs in preclinical development could improve overall therapy for parasitic infections even when their mechanisms of action are unknown. In this review, a number of heterocyclic compounds (diamidine, guanidine, quinoline, benzimidazole, thiazole, diazanaphthalene, and their derivatives) reported as antiprotozoal agents are discussed as options for developing new pharmacological treatments for parasitic diseases.

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Source
http://dx.doi.org/10.2174/0929867327666200303170000DOI Listing

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