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Int J Parasitol Drugs Drug Resist ; 7(1): 120-129, 2017 04.
Article in English | MEDLINE | ID: mdl-28285258

ABSTRACT

Drugs against malaria are losing their effectiveness because of emerging drug resistance. This underscores the need for novel therapeutic options for malaria with mechanism of actions distinct from current antimalarials. To identify novel pharmacophores against malaria we have screened compounds containing structural features of natural products that are pharmacologically relevant. This screening has identified a 4-nitro styrylquinoline (SQ) compound with submicromolar antiplasmodial activity and excellent selectivity. SQ exhibits a cellular action distinct from current antimalarials, acting early on malaria parasite's intraerythrocytic life cycle including merozoite invasion. The compound is a fast-acting parasitocidal agent and also exhibits curative property in the rodent malaria model when administered orally. In this report, we describe the synthesis, preliminary structure-function analysis, and the parasite developmental stage specific action of the SQ scaffold.


Subject(s)
Aminoquinolines/pharmacology , Antimalarials/pharmacology , Drug Discovery , Plasmodium falciparum/drug effects , Styrenes/pharmacology , Administration, Oral , Aminoquinolines/chemistry , Aminoquinolines/therapeutic use , Animals , Antimalarials/chemistry , Antimalarials/therapeutic use , Erythrocytes/parasitology , Life Cycle Stages/drug effects , Malaria/drug therapy , Malaria/parasitology , Merozoites/drug effects , Parasitic Sensitivity Tests , Plasmodium berghei , Plasmodium falciparum/growth & development , Rats , Styrenes/chemistry , Styrenes/therapeutic use
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