氯喹
长时程增强
恶性疟原虫
抗疟药
药理学
生物
激进的
化学
药品
疟疾
立体化学
生物化学
免疫学
受体
作者
Rolf W. Winter,Ken Cornell,Linda L. Johnson,Marina Ignatushchenko,David J. Hinrichs,Michael K. Riscoe
标识
DOI:10.1128/aac.40.6.1408
摘要
We have discovered a remarkable synergistic antimalarial interaction between rufigallol and the structurally similar compound exifone. The synergistic effects were produced in chloroquine-susceptible and chloroquine-resistant clones of Plasmodium falciparum. The degree of potentiation as estimated by standard isobolar analysis was approximately 60-fold for experiments initiated with asynchronous parasites. The most pronounced synergism was observed in experiments with synchronized trophozoite-infected erythrocytes, in which the degree of synergy was at least 300-fold. While the mechanism underlying this drug potentiation remains unresolved, it is hypothesized that rufigallol acts in pro-oxidant fashion to produce oxygen radicals inside parasitized erythrocytes. These radicals would attack exifone, thereby initiating its transformation into a more potent compound, a xanthone.
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