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双螺-1,2,4,5-四氧杂环己烷:一类新型抗疟过氧化物。

Dispiro-1,2,4,5-tetraoxanes: a new class of antimalarial peroxides.

作者信息

Vennerstrom J L, Fu H N, Ellis W Y, Ager A L, Wood J K, Andersen S L, Gerena L, Milhous W K

机构信息

College of Pharmacy, University of Nebraska Medical Center, Omaha 68198-6025.

出版信息

J Med Chem. 1992 Aug 7;35(16):3023-7. doi: 10.1021/jm00094a015.

Abstract

Dispiro-1,2,4,5-tetraoxanes 2-4 were synthesized as potential peroxide antimalarial drugs. They had curative activity against Plasmodium berghei in vivo at single doses of 320 and 640 mg/kg which confirms earlier unpublished data. Moreover, artemisinin (1) and 4 had equivalent ED50's against P. berghei in vivo in the multiple-dose Thompson test; neither showed any evidence of acute toxicity at total doses of more than 12 g/kg. Dispiro-1,2,4,5-tetraoxane 4 had IC50's comparable to those of 1 against Plasmodium falciparum clones in vitro. These results confirm the potential of dispiro-1,2,4,5-tetraoxanes as a new class of inexpensive peroxide antimalarial drugs.

摘要

双螺环-1,2,4,5-四氧杂环己烷2-4被合成为潜在的过氧化物抗疟药物。它们在单剂量320和640 mg/kg时对伯氏疟原虫具有体内治愈活性,这证实了早期未发表的数据。此外,青蒿素(1)和4在多剂量汤普森试验中对伯氏疟原虫的体内ED50相当;在总剂量超过12 g/kg时,两者均未显示出任何急性毒性迹象。双螺环-1,2,4,5-四氧杂环己烷4在体外对恶性疟原虫克隆的IC50与1相当。这些结果证实了双螺环-1,2,4,5-四氧杂环己烷作为一类新型廉价过氧化物抗疟药物的潜力。

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