Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria
| Autor: | Suzete Maria Almeida, Kangsa Amporndanai, Juliana Calit, Arlene G. Corrêa, Anna Caroline Campos Aguiar, Glaucius Oliva, Juliana Oliveira de Souza, Daniel Y. Bargieri, Camila Lima Zanini, Dhelio Batista Pereira, S. Samar Hasnain, Fabio C. Cruz, Guilherme Eduardo de Souza, Svetlana V. Antonyuk, Everton M. da Silva, Rafael Victorio Carvalho Guido |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Inhibitor
medicine.drug_class Plasmodium falciparum 4(1H)-Quinolone Computational biology Biology medicine.disease Quinolone Malaria RS1-441 PLASMODIUM FALCIPARUM Other systems of medicine Lead (geology) Pharmacy and materia medica parasitic diseases medicine Profiling (information science) Plasmodium vivax Cytochrome bc1 complex RZ201-999 |
| Zdroj: | European Journal of Medicinal Chemistry Reports, Vol 3, Iss, Pp 100012-(2021) Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual) Universidade de São Paulo (USP) instacron:USP |
| ISSN: | 2772-4174 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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