Table 2: Anticonvulsant activity of 6-(p-Chloro/p-methyl/m-nitro-phenyl)-4-arylidene-4,5-dihydropyridazin-3(2H)-one compounds (3a-m) against isoniazid (INH) induced method.

S.
No.
Groups Onset of convulsion
(sec)
No. of convulsion Recovery
(%)
1 Compd 3a 36.2±6.27 γa 2.5±0.22 80
2 Compd 3b 47±4.50 γc 2.8±0.25 80
3 Compd 3c 48.6±3.87γc 2.5±0.24 60
4 Compd 3d 34.6±3.24γ 2.4±0.36 100
5 Compd 3e 35.2±6.98γ 2.6±0.35 100
6 Compd 3f 42.6±2.62 γc 2.0±0.32 80
7 Compd 3g 46.8±2.06γc 2.4±0.34 80
8 Compd 3h 48±1.82 γc 2.4±0.26 80
9 Compd 3i 47.6±4.24 γc 2.2±0.24 60
10 Compd 3j 48.2±4.18 γc 2.6±0.18 100
11 Sod. VPA 130.2 ± 2.15 1.4±0.22 100
12 PHT sod. 0.00 0.00 100
13 Control 26.16±.094 3.2±0.20 00

Standard drug: PHT sodium (25mg/kg) and Sodium VPA (100mg/kg), Tested drugs: (50mg/kg), Control group: INH-250mg/kg+0.5 % CMC in distilled water; n=5 (No. of animals in each group); *Value represents mean ± S.E.M. cP< 0.001 when compared to control group γP< 0.001 when compared to standard drug sodium VPA.