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. Author manuscript; available in PMC: 2014 Nov 27.
Published in final edited form as: J Med Chem. 2013 Nov 11;56(22):9019–9030. doi: 10.1021/jm400894u

Table 2.

Oral Mouse MES ED50 Data for Selected Compoundsa

cmpd ED50 (mg/kg, po) 95% CI neurotoxicityb
4 120c -- d
(S)-5 199 183–222 0/8 (250)
10a 124 85–173 6/8 (300)
10b 104 91–128 0/8 (150)
10d 230 171–281 2/8 (350)
10e 161 138–192 3/8 (300)
10h 296 202–473 3/8 (600)
11a 131 120–141 1/8 (150)
12 267 232–299 4/8 (300)
3 119c 112–126 d
phenytoin 9.0e TD50 = 86.7e
1 43.8f TD50 = 389g
a

Maximal electroshock seizure model, at 1 h post dosing, performed at NeuroAdjuvants. CI, 95% confidence interval.

b

Mouse rotorod toxicity, at the dose in mg/kg given in parentheses. The effect is presented as the number of animals responding out of the total number of animals tested.

c

Performed in house; result at 3 h post dosing (time of peak effect).

d

See text for rat data.

e

At 2 h; ref 3a.

f

At 1 h; ref 6.

g

At 1 h; ref 3a.