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. Author manuscript; available in PMC: 2013 Sep 13.
Published in final edited form as: J Med Chem. 2012 Aug 27;55(17):7892–7899. doi: 10.1021/jm3009986

Table 4.

In vivo antimalarial efficacy using a single oral dose of 6 mg/kg trioxane and 18 mg/kg mefloquine hydrochloride in P. berghei-infected mice.

Trioxane Average survival (days) after
infection
% Suppression of parasitemia
(on day 3 post infection)
11a 12.8 (13, 13, 13, 12) >99.9%
11b 18.5 (30, 16, 15, 13) >99.9%
11c 17.8 (28, 17, 13, 13) >99.9%
11d 19.3 (29, 17, 17, 14) >99.9%
11e 18.8 (30, 17, 15, 13) 99.9%
11f 21.8 (30, 30, 15, 12) >99.9%
11g 16.5 (28, 14, 12, 12) >99.9%
11h 25.3 (30, 29, 27, 15) >99.9%
11i 14.5 (17, 15, 13, 13) 99.9%
12a 24.5 (30, 30, 21, 17) >99.9%
12b 19.3 (30, 17, 15, 15) >99.9%

12c 29.8 (30, 30, 30, 29) 99.9%

12d 22.0 (30, 28, 17, 13) 99.9%
13a 23.0 (30, 29, 17, 16) >99.9%
13b 22.3 (30, 29, 17, 13) >99.9%
14a 26.3 (29, 28, 27, 21) >99.9%
14b 19.5 (29, 20, 15, 14) >99.9%
15 19.8 (30, 17, 17, 15) 99.9%

Controls
Infected (no drug) 8.0 (10, 8, 7, 7) 0%
Artemether + mefloquine-HCl 16.5 (28, 13, 13, 12) >99.9%
Mefloquine-HCl only 14.0 (17, 13, 13, 13) >99.9%