XU De-yu, CHEN Xiong, YIN Xiang-sheng , NING Xiao-min, . STUDIES ON SYNTHETIC ANTIMALARIALS Ⅵ.THE SYNTHESIS AND ANTIMALARIAL ACTIVITY OF SOME NEW PIPERAQUINE ANALOGUES,TRIPIPERAQUINESJ. Acta Pharmaceutica Sinica, 1983, 18(1): 20-24.
Citation: XU De-yu, CHEN Xiong, YIN Xiang-sheng , NING Xiao-min, . STUDIES ON SYNTHETIC ANTIMALARIALS Ⅵ.THE SYNTHESIS AND ANTIMALARIAL ACTIVITY OF SOME NEW PIPERAQUINE ANALOGUES,TRIPIPERAQUINESJ. Acta Pharmaceutica Sinica, 1983, 18(1): 20-24.

STUDIES ON SYNTHETIC ANTIMALARIALS Ⅵ.THE SYNTHESIS AND ANTIMALARIAL ACTIVITY OF SOME NEW PIPERAQUINE ANALOGUES,TRIPIPERAQUINES

  • A series of new piperaquine analogues with three piperazinyl groups in side chain was synthesized. Primary screening test on mice-infected with blood form parasites of Plasmodium berghei showed that all of these compounds were active. Compounds Ⅳc,g,h were shown to completely suppress the parasitemia of infected mice at the dose of 3 mg/kg for 3 consecutive days. In protection test on the same screening system, two compounds appeared to have a marked long-lasting protective effect against the blood infection of P. berghei in mice. Compound Ⅳa is the same compound reported as M 1020 in reference number 8. Compound Ⅳd protected mice against intervening challenge with P. berghei for 45 days following a single oral dose of 600 mg/kg. It also exhibited long-lasting protective effect of about 20 to 25 days against P. cynomolgi in monkeys.
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