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. Author manuscript; available in PMC: 2014 Mar 28.
Published in final edited form as: J Med Chem. 2013 Mar 7;56(6):2630–2641. doi: 10.1021/jm400058j

Table 2.

In Vivo Antimalarial Efficacy Using a Single Oral Dose of Trioxane Combined with Mefloquine Hydrochloride or Lumefantrine in P.berghei Infected Mice

trioxane single oral dose (mg/kg)
survival after infection (days) avg survival % parasitemia suppression1
trioxane adjuvant dose
E-26 6 mefloquine 18 16, 35, 37, 60 37.0 >99.9

26 6 mefloquine 18 16, 60, 60, 60 49.0 >99.9
26 6 lumefantrine 18 13, 16, 16, 60 26.3 >99.9
26 150 none 0 7, 7, 9, 10 8.3 98

27 6 mefloquine 18 16, 60, 60, 60 49.0 >99.9
27 6 lumefantrine 18 16, 29, 60, 60 41.3 >99.9
27 150 none 0 7, 60, 60, 60 46.8 >99

28 6 mefloquine 18 15, 29, 60, 60 41 >99.9
30 6 mefloquine 18 18, 20, 20, 37 23.8 >99.9

31 6 mefloquine 18 35, 60, 60, 60 53.8 >99.9
graphic file with name nihms450796t3.jpg
31 150 none 0 7, 60, 60, 60 46.8 >99.9
controls:
vehicle (no drug) 0 0 6, 7, 7, 15 8.8 0
artemether(4b) 6 mefloquine 18 29, 29, 36, 60 38.5 >99.9
artemether(4b) 6 lumefantrine 18 15, 16, 16, 29 19.0 >99.9
mefloquine 0 18 15, 16, 30, 31 23.0 >99.9
lumefantrine 0 18 7, 7, 7, 35 14.0 >99.9
1

determined on day 3 post infection