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. Author manuscript; available in PMC: 2015 Jun 1.
Published in final edited form as: Bioorg Med Chem Lett. 2014 Apr 16;24(11):2440–2443. doi: 10.1016/j.bmcl.2014.04.025

Table 1.

In vivo antimalarial efficacy using a single oral dose of trioxane dimer (6 mg/kg) combined with mefloquine hydrochloride (18 mg/kg) in P. berghei ANKA-infected mice

trioxane survival after infection (days) avg survivala % parasitemia suppressionb
12b 14, 20, 21, 23 19.5 >99.9
14a 14, 15, 15, 30 18.5 >99.9
14b 13, 23, 30, 30 24 >99.9
graphic file with name nihms591228t1.jpg
14d 23, 21, 23, 30 24.3 >99.9
graphic file with name nihms591228t2.jpg
14f 21, 14, 15, 20 17.5 >99.9
14g 23, 21, 21, 30 23.8 >99.9
14h 21, 20, 23, 30 23.5 >99.9
14i 30, 23, 14, 30 24.3 >99.9
14j 27, 20, 21, 30 24.5 >99.9
14k 30, 20, 14, 23 21.8 >99.9
graphic file with name nihms591228t3.jpg
15a 23, 20, 21, 29 23.3 >99.9
graphic file with name nihms591228t4.jpg
15c 15, 23, 30, 30 24.5 >99.9
controls:
vehicle (no drug) 6, 7, 7, 8 7 0c
artemether (2) 6 mg/kg + mefloquine HCl 18 mg/kg 23, 27, 13, 23 21.5 >99.9
mefloquine HCl 18 mg/kg alone 13, 15, 23, 20 17.8 >99.9
a

Best results are in bold type.

b

Denotes determination on day 3 after infection.

c

An average of 10% parasitemia was determined on day 3 after infection.