Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria



de Souza, Juliana O, Almeida, Suzete M ORCID: 0000-0003-4247-2228, Souza, Guilherme E ORCID: 0000-0003-3278-6688, Zanini, Camila L, da Silva, Everton M, Calit, Juliana, Bargieri, Daniel Y, Amporndanai, Kangsa, Antonyuk, Svetlana, Hasnain, S Samar ORCID: 0000-0002-2854-4718
et al (show 6 more authors) (2021) Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, 3. p. 100012.

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Abstract

4(1H)-quinolone is an attractive template for antimalarial drug discovery campaigns. Given the current global increase in drug and insecticide resistance, the discovery of new antimalarial drugs is an urgent goal for the fight against malaria. Here, the synthesis and antiplasmodial profiling of a series of 4(1H)-quinolone derivatives are reported. Four compounds showed inhibitory activities in submicromolar range against a panel of sensitive and resistant Plasmodium falciparum strains (IC50s ​= ​0.07–0.48 ​μM) and neither cytotoxic (SI ​> ​210) nor hemolytic activities were observed. Representative compounds of the series showed slow-acting in vitro inhibition, enhanced inhibitory activities over the later erythrocytic forms of the parasite, and submicromolar activity against the ookinete stage (IC50ook ​= ​0.7 ​μM). Evaluation of the mechanism of action indicated that the frontrunner, compound 4 (LSPN182), is a potent (IC50Pfbc1 ​= ​0.5 ​μM) and selective (SI ​> ​120) inhibitor for the cytochrome bc1 complex of P. falciparum. Moreover, the frontrunner exhibited considerable activity against clinical field isolates of both P. falciparum and P. vivax (IC50s of 0.5 and 1.5 ​μM, respectively), a noticeable synergic inhibitory behavior when combined with the antimalarial proguanil (FICindex < 1), and modest oral efficacy at 50 ​mg/kg in a mouse model of P. berghei malaria (45% reduction in parasitemia on day 7 postinfection). Hence, the 4(1H)-quinolone derivatives are attractive chemotypes endowed with relevant in vitro, ex vivo, and in vivo activity.

Item Type: Article
Divisions: Faculty of Health and Life Sciences
Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology
Depositing User: Symplectic Admin
Date Deposited: 17 Apr 2023 09:45
Last Modified: 17 Apr 2023 09:45
DOI: 10.1016/j.ejmcr.2021.100012
Open Access URL: https://doi.org/10.1016/j.ejmcr.2021.100012
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3169609