Indoloquinoline Alkaloids as Antimalarials: Advances, Challenges, and Opportunities

Author:

Parvatkar Prakash T.1ORCID,Diagne Khaly1,Zhao Yingzhao1,Manetsch Roman1234ORCID

Affiliation:

1. Department of Chemistry and Chemical Biology Northeastern University Boston MA 02115 USA

2. Department of Pharmaceutical Sciences Northeastern University Boston MA 02115 USA

3. Center for Drug Discovery Northeastern University Boston MA 02115 USA

4. Barnett Institute of Chemical and Biological Analysis Northeastern University Boston MA 02115 USA

Abstract

AbstractMalaria infections affect almost half of the world‘s population, with over 200 million cases reported annually. Cryptolepis sanguinolenta, a plant native to West Africa, has long been used across various regions of Africa for malaria treatment. Chemical analysis has revealed that the plant is abundant in indoloquinolines, which have been shown to possess antimalarial properties. Cryptolepine, neocryptolepine, and isocryptolepine are well‐studied indoloquinoline alkaloids known for their potent antimalarial activity. However, their structural rigidity and associated cellular toxicity are major drawbacks for preclinical development. This review focuses on the potential of indoloquinoline alkaloids (cryptolepine, neocryptolepine, and isocryptolepine) as scaffolds in drug discovery. The article delves into their antimalarial effects in vitro and in vivo, as well as their proposed mechanisms of action and structure‐activity relationship studies. Several studies aim to improve these leads by reducing cytotoxicity while preserving or enhancing antimalarial activity and gaining insights into their mechanisms of action. These investigations highlight the potential of indoloquinolines as a scaffold for developing new antimalarial drugs.

Funder

Northeastern University

Publisher

Wiley

Reference244 articles.

1.  

2. The 2023 WHO World malaria report

3. World Health Organization.World Malaria Report 2023; Geneva 2023.

4.  

5. Rapid Diagnostic Tests for Malaria Parasites

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