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Tetracyclines as antiparasitic agents: lipophilic derivatives are highly active against Giardia lamblia in vitro.

机译:四环素类药物作为抗寄生虫剂:亲脂性衍生物在体外对贾第鞭毛虫具有高度活性。

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摘要

Comparisons of the inhibitory activities of different tetracyclines have been reported for Plasmodium falciparum but no other parasites. The in vitro response of the intestinal parasite Giardia lamblia to six tetracyclines in current use was determined. In addition, the experimental drug thiacycline (EMD 33,330) was evaluated. Three groups were discerned, with representative 50 and 90% inhibitory concentrations of, respectively, 36 and 130 (tetracycline), 6.4 and 22 (doxycycline), and 1.8 and 3.4 (thiacycline) micrograms/ml. These dramatic differences in activity correlate with increased lipophilicity.
机译:已报道比较了不同四环素对恶性疟原虫的抑制活性,但没有其他寄生虫。确定了当前使用的肠道寄生虫贾第鞭毛虫对六种四环素的体外反应。另外,评估了实验药物噻环素(EMD 33,330)。识别出三组,分别具有代表性的50和90%抑制浓度,分别为36和130(四环素),6.4和22(多西环素)以及1.8和3.4(噻环素)微克/毫升。活性的这些显着差异与亲脂性增加有关。

著录项

  • 作者

    Edlind, T D;

  • 作者单位
  • 年度 1989
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

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