Design and Synthesis of Some Novel 4-( 4-substituted aryl ) Semicarbazones as Anticonvulsant Agents

In the present study, a series of 4-(4-substituted aryl) semicarbazones were synthesized from substituted anilines and subsequently evaluated for their anticonvulsant activities. The anticonvulsant activities were established by the anticonvulsant drug development (ADD) programme NIH, USA using experimental animal, adult male FCM mice (20-25 g) and adult Sprague-Dawley rats (100-150 g) and screened against electroshock seizure, subcutaneous metrazole and minimal neurotoxicity tests in mice. Compound 7 was found equipotent to carbamazepine in both MES and ScPTZ tests. This study has highlighted the importance of distal alkyl chain which infl uences the anticonvulsant activity.

Epilepsy is the most common serious neurological disorder worldwide [1] .The anticonvulsant properties have been displayed by various hydrazones [2] , amides [3] and carbamides [4] .The prime need was to search a molecule which could complement to all these structures.Recently, Unverferth et al. suggested a pharmacophore model for structurally different anticonvulsant containing aryl ring, electron donor and hydrogen bonding functions [5] .
The lipophilic aryl ring with chloro, bromo or nitro groups have been found to be essential for anticonvulsant activity.The distal aryl ring is also implicated at the binding site.The hydrogen bonding in semicarbazone series has been suggested by Dimmock et al. [6,7] to be the terminal -NHCONH 2 group.In continuation, Pandeya et al. [8,9] suggested HBD to be adjacent to the lipophilic aryl ring and another hydrophobic centre for activity.Generally, the structural requirements for activity in the maximal electroshock (MES) screen have been found the presence of a large hydrophobic group (phenytoin) and for subcutaneous pentylene tetrazole (ScPTZ) screen, a smaller and less hydrophobic group (ethosuximide) near to two electron-donor atoms [10] .In this report, here we demonstrate the lipophilic aryl ring substitution in semicarbazones along with nitro, chloro and bromo groups as novel anticonvulsant agents.
Melting points of the synthesized compounds were taken by the open capillary method and are uncorrected.UV (EtOH-Band λ max , nm) and IR (KBr, cm -1 ) spectra were consistent with the assigned structures recorded on Jasco Model 7800 and Jasco FT/IR-5300 instruments respectively and 1 H NMR (DMSO d 6 -TMS, ppm) spectra were recorded Jeol FX 90Q FT spectroscope using TMS as internal standard.Chemical shift are quoted in δ (ppm) units relative to TMS.Purity of the synthesized compounds were checked by TLC using silica gel G (Merck, Germany) and chloroform methanol (9:1) solvent system.4-substituted semicarbazone derivatives were prepared in three steps as follows: 4-substituted aniline (0.1 mol) was dissolved in 10 ml of glacial acetic acid (GAA) and diluted to 100 ml with water.Equimolar quantity (0.1 mol) of sodium cyanate in 50 ml of warm water was added in previous solution with stirring.The reaction mixture was allowed to stand for 30 min, and then it was fi ltered, washed, dried and recrystallized from boiling water.
To a solution of 4-substituted phenyl urea (0.1 mol) in 20 ml ethanol, an equimolar (0.1 mol) quantity of hydrazine hydrate was added.The reaction mixture was made alkaline by adding 4 g of NaOH, was May -June 2010 A solution of p-phenyl semicarbazide (0.01 mol) and an equimolar (0.01 mol) quantity of appropriate carbonyl compound was refl uxed for 30 min in the presence of glacial acetic acid (1-1.5 ml).The product obtained after cooling was fi ltered and recrystallised from 95% ethanol to give pure compounds (Scheme 1).The characterization data of the compounds are reported (Table 1).programme [11] .Adult male FCM mice (20-25 g) and adult male Sprague Dawley rats (100-150 g) were used as experimental animals.The animals were maintained on an adequate diet and allowed free access to food and water except during the short time they are removed from their cages for testing.The animals were maintained at room temperature (25-30°).Number of animals was used from 4-6 depending upon the nature of test.
Initially all the compounds dissolved in polyethylene glycol were administered intraperitoneally (0.01 ml /g body weight in mice and 0.004 ml /g body weight in rats) at a dose of 30, 100, and 300 mg/kg to all the animals respectively.Compounds were screened for anticonvulsant activity by maximal electroshock seizure (MES), subcutaneous metrazole (ScMet) and Minimal neurotoxicity (TOX) test in mice.
MES or maximal seizure pattern test, in which an electrical stimulus of 0.2 s in duration (50 mA in mice and 150 mA in rat at 60Hz) was delivered via corneal electrodes primed with an electrolyte solution containing an anesthetic agent.Mice are tested at 30 min and 4 h following doses of 30, 100 and 300 mg/ kg of test compound.Abolition of the hindlimb tonic extensor component indicates the test compound's ability to inhibit MES-induced seizure spread [12] .
The subcutaneous pentylenetetrazol (metrazol) seizure test (scPTZ) was performed using a dose of pentylenetetrazol (70 mg/kg in Sprague Dawley rats) to produce clonic seizures lasting for a period of at least five seconds in 97 per cent (CD97) of animals tested.At the anticipated time of testing the convulsant is administered subcutaneously.The test compound is administered intraperitoneally in mice and orally in rats.Animals are observed over a 30 min period.Absence of clonic spasms in the observed time period indicates a compound's ability to abolish the effect of pentylenetetrazol on seizure threshold [13] .
Minimal neurotoxicity (TOX) was evaluated in rats by examining them for behavioral toxicity using the positional sense test and a gait and stance test.The mice were trained to stand on an accelerating rotarod of diameter 3.2 cm, which rotated at 10 rev/min.Animals were given intraperitoneal injections of the test compounds in the doses of 30, 100 and 300 mg/ kg body weight.Neurotoxicity was indicated by the inability of the animal to maintain equilibrium on the rod for at least one minute in each of the three trials [14] .
The UV spectrum shows presence of chromophores in the 4-substituted aryl/alkyl semicarbazones.The benzene ring absorption is in the range of 200-205 nm pertaining to K-band.The π-π * transition.K-band of substituted p-nitroaniline was very strong λ max 375-380 nm.The halo substituted derivatives absorbed at 265 nm.The formation of the substituted hydrazones and semicarbazones were confirmed with the formation of C=N band in all spectra from 1500-1620 cm -1 .The CONH stretching for amides was observed in the 4-substituted aryl/alkyl semicarbazones at about 3180-3320 cm Generally MES active compounds are considered to exhibit activity in grandmal epilepsy, contain larger hydrophobic center (phenytoin) [15] and ScMet active compounds are considered petitmal active, contain smaller hydrophobic centers (ethosuximide) [16] .This study has highlighted the importance of distal alkyl chain which infl uences the anticonvulsant activity.The distal hydrophobic side perhaps may be differentiating the kind of anticonvulsant activity.

TABLE 3 : MES TEST UPON ORAL ADMINISTRATION OF COMPOUND 7 IN RATS
Number of animals affected/ number of animals used, α Maximal electroshock seizure, β Neurotoxicity, Compound 7 was administered at a dose of 30 mg kg -1 in rats a . a