伯氏疟原虫
恶性疟原虫
体内
体外
化学
噻吩
疟原虫(生命周期)
药理学
生物
立体化学
生物化学
疟疾
有机化学
寄生虫寄主
免疫学
生物技术
万维网
计算机科学
作者
F Tedlaouti,M. Gasquet,F. Delmas,P. Timon‐David,Madadi Ne,Patrice Vanelle,José Maldonado
出处
期刊:PubMed
日期:1990-09-01
卷期号:45 (5): 306-10
摘要
Various hydrazones of thiophene carboxaldehyde were tested in vitro on two Plasmodium falciparum strains and in vivo on mice experimentally infected with Plasmodium berghei. These hydrazones were obtained by condensation of appropriate hydrazines with thiophene-2-carboxaldehyde (series 1), thiophene-3- carboxaldehyde (series 2) and 5-Nitrothiophene-2-carboxaldehyde (series 3). Compounds of series 3, 5-Nitrothiophene-2-carboxaldehyde presented significant effects in vitro. In vivo tests confirmed the antimalarial activity observed in vitro with two compounds of this series.
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