4.7 Article

Synthesis of new esters and oximes with 4-aminobicyclo [2.2.2] octane structure and evaluation of their antitrypanosomal and antiplasmodial activities

Journal

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 41, Issue 8, Pages 970-977

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2006.04.002

Keywords

4-aminobicyclo[2.2.2]octane derivatives; Trypanosoma b. rhodesiense; Plasmodium falciparum; in vitro assays; O-methyloximes; aromatic esters

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New 4-amino-6,7-diphenylbicyclo[2.2.2]octane derivatives, esters of bicyclo[2.2.2]octan-2-ols and O-methyl oximes of bicyclo[2.2.2]octan-2ones were synthesised. Their activities against Trypanosoma brucei rhodesiense (STIB 900) and their activity against the K1 strain of Plasmodium falciparum (resistant to chloroquine and pyrimethamine) were determined by use of microplate assays. The cytotoxicity was assessed using L6 cells. The antiprotozoal activities of the new compounds are compared with those of former prepared derivatives and drugs in use. Structure-activity relationships are discussed. (c) 2006 Elsevier SAS. All rights reserved.

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