Design of Antimalarial Compounds on Quinoline Scaffold: From Plant to Drug
- Authors: Paulo F. S. Santos Júnior1, Igor J. S. Nascimento2, Geraldo J. S. Neto3, Rafael J. M. Omena4, Thiago M. Aquino5, João X. Araújo-Júnior6, Mario R. Meneghetti7, Edeildo F. Silva-Júnior8
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View Affiliations Hide Affiliations1 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil 2 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil 3 Group of Catalysis and Chemical Reactivity, Chemistry and Biotechnology Institute, Federal University of Alagoas, Maceió, Brazil 4 Group of Catalysis and Chemical Reactivity, Chemistry and Biotechnology Institute, Federal University of Alagoas, Maceió, Brazil 5 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil 6 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil 7 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil 8 Institute of Chemistry and Biotechnology, Federal University of Alagoas, Maceió, Brazil
- Source: Alkaloids and Other Nitrogen-Containing Derivatives , pp 189-237
- Publication Date: June 2023
- Language: English
Plasmodium species are responsible for a high incidence of cases and resistance, even with several approved drugs. Quinoline derivatives are recognized as a source of active compounds, where tafenoquine has been recently approved. Cases of resistance and the indiscriminate use of anti-malarials against COVID-19 have negatively contributed to eradicating this disease. In this context, modifications at 2- or 4-amino positions from the quinoline scaffold or even its metal complexes have shown promising advances in the field, especially against resistant strains, such as 3D7, W2, D10, Dd2, K1 , and FCR-3. In this chapter, we discussed all aspects involving such compounds, presenting their results based on SAR analysis and recent contributions/advances involving this classic scaffold arising from nature.
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