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January 18, 2026Current Drug Therapy0 citations

Biological Targets in Leishmaniasis and the Identification of the Next Generation of Antileishmanial Compounds

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PSPatrick O. SakyiDODorcas Osei-SafoSKSamuel Kojo Kwofie

Key Points

  • The aim is to identify viable biological targets in Leishmania to facilitate the development of new antileishmanial drugs.
  • Reviewed 260 articles between 1981 and 2025
  • Summarized strategies in drug design and biological target identification
  • Analyzed biochemical reactions and inhibitory activities of identified compounds
  • Outlined synthetic strategies for key chemotypes
  • Identified critical biological targets involved in Leishmania survival
  • Revealed promising inhibitors across multiple pathways
  • Evaluated multitarget inhibitors, outlining both advantages and disadvantages
  • Proposed actionable steps to improve antileishmanial agent development

Abstract

With increasing mortality and morbidity, leishmaniasis remains a global health burden. The lack of vaccines and limited drug options for treatment, each with low efficacy and severe toxicities, highlights the urgent need for new therapeutics. Our review of 260 articles (1981-2025) provides comprehensive insights, emphasizing the critical identifica-tion and characterization of viable biological targets in Leishmania for efficient drug devel-opment. We summarize the various strategies utilized in the drug design pipeline, detailing how these approaches have revealed key biological targets involved in parasite survival, virulence, and pathogenesis, and have identified promising inhibitors across metabolic and non-metabolic pathways. We report the biochemical reactions and inhibitory activities (IC50) of these compounds against their respective targets. Additionally, we outline the synthetic strategies for key chemotypes and identify ongoing challenges and future directions in an-tileishmanial agent research. Importantly, our review evaluates multitarget inhibitors, high-lighting their pros and cons and proposing actionable steps to leverage these molecules to overcome leishmaniasis.

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Cite This Study

Sakyi et al. (2026) studied this question.

synapsesocial.com/papers/696c77afeb60fb80d1395f20https://doi.org/10.2174/0115748855407118251114095002
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