Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374137 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
The in vitro activity of newly synthesized bis-(chlorophenyl)-azabicyclo[3.2.2]nonanes and bis-(chlorophenyl)-bicyclo[2.2.2]octanes against Plasmodium falciparum K1 (resistant to chloroquine and pyrimethamine) and Trypanosoma brucei rhodesiense was investigated. Especially the bis-(chlorophenyl)-azabicyclo[3.2.2]nonanes exhibit promising antitrypanosomal activity and were tested in vivo against Trypanosoma brucei brucei featuring moderate activities.
Graphical abstractThe in vitro activity of newly synthesized bis-(chlorophenyl)-azabicyclo[3.2.2]nonanes and bis-(chlorophenyl)-bicyclo[2.2.2]octanes against Plasmodium falciparum K1 (resistant to chloroquine and pyrimethamine) and Trypanosoma brucei rhodesiense was investigated.Figure optionsDownload full-size imageDownload as PowerPoint slide