Discovery and Structure-Activity Relationships of Quinazolinone-2-carboxamide Derivatives as Novel Orally Efficacious Antimalarials.
J Med Chem
; 64(17): 12582-12602, 2021 09 09.
Article
en En
| MEDLINE
| ID: mdl-34437804
ABSTRACT
A phenotypic high-throughput screen allowed discovery of quinazolinone-2-carboxamide derivatives as a novel antimalarial scaffold. Structure-activity relationship studies led to identification of a potent inhibitor 19f, 95-fold more potent than the original hit compound, active against laboratory-resistant strains of malaria. Profiling of 19f suggested a fast in vitro killing profile. In vivo activity in a murine model of human malaria in a dose-dependent manner constitutes a concomitant benefit.
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Malaria Falciparum
/
Quinazolinonas
/
Antimaláricos
Límite:
Animals
/
Humans
Idioma:
En
Año:
2021
Tipo del documento:
Article