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1. Dual role of azo compounds in inhibiting Plasmodium falciparum adenosine deaminase and hemozoin biocrystallization

Author

Buabarn Kuaprasert, Penchit Chitnumsub, Ubolsree Leartsakulpanich, Pinpunya Riangrungroj, Wipa Suginta, Saovanee Leelayoova, Mathirut Mungthin, Naruemon Sitthichot, Siriluk Rattanabunyong, Duangnapa Kiriwan, and Kiattawee Choowongkomon

Subjects
Biomineralization, Antimalarials, Infectious Diseases, Adenosine Deaminase, Plasmodium falciparum, Immunology, Drug Resistance, Adenosine Deaminase Inhibitors, Chloroquine, Parasitology, General Medicine, Ligands, Azo Compounds
Abstract

Protein-ligand (GOLD) docking of the NCI compounds into the ligand-binding site of Plasmodium falciparum adenosine deaminase (PfADA) identified three most active azo compounds containing 4-[(4-hydroxy-2-oxo-1H-quinolin-3-yl) moiety. These compounds showed IC

Published
2022
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