Current Research on Antiepileptic Compounds

Abstract

Epilepsy affects about 1% of the world’s population. Due to the fact all antiepileptic drugs (AEDs) have some undesirable side effects and about 30% of epileptic patients are not seizure-free with the existing AEDs, there is still an urgent need for the development of more effective and safer AEDs. Based on our research work on antiepileptic compounds and other references in recent years, this review covers the reported work on antiepileptic compounds which are classified according to their structures. This review summarized 244 significant anticonvulsant compounds which are classified by functional groups according to the animal model data, although there are some limitations in the data. This review highlights the properties of new compounds endowed with promising antiepileptic properties, which may be proven to be more effective and selective, and possibly free of unwanted side effects. The reviewed compounds represent an interesting possibility to overcome refractory seizures and to reduce the percentage of patients with a poor response to drug therapy.

1. Introduction

Epilepsy is one of the more common and frequent neurological disorders in man, characterized by excessive temporary neuronal discharges resulting in uncontrolled convulsions that affect more than 2 million Americans and 60 million people worldwide [1]. If not treated, it is associated with progressively impaired cognition and function, brain damage, and other neurologic deficits. Although in many cases, epilepsy can be adequately controlled through administration of antiepileptic drugs (AEDs), it is estimated that roughly 20%–30% of patients have seizures that are resistant to available medical therapies [2,3,4].

Conventional AEDs like phenobarbital, primidone, phenytoin, carbamazepine, ethosuximide and the benzodiazepines are widely used. All currently approved antiepileptic drugs have dose-related toxicity and idiosyncratic side effects [5,6,7,8,9,10,11]. Therefore, the search for a newer, more effective, more selective agent with lesser side effects continues to be an area of investigation of medicinal chemists worldwide.

Anticonvulsant activities of new synthesized compounds were evaluated according to the Antiepileptic Drug Development Program of the National Institutes of Health (NIH) with the maximal electroshock (MES) test, the subcutaneous pentylenetetrazol (sc-PTZ) test, and the neurotoxicity was evaluated by the rotarod neurotoxicity test.

2. The Quinoline Functional Group

Quinoline is nitrogen-containing heterocyclic aromatic compound. Pharmacologically active substances display a broad range of biological activity. Quinoline has been found to possess anti-malarial, antibacterial, antifungal, anthelmintic, cardiotonic, anticonvulsant, anti-inflammatory, and analgesic activity. Our laboratory has studied a lot of quinoline derivatives for antiepileptic activity [12,13,14,15,16,17,18,19,20,21,22,23].

Xie et al., reported a new series of 7-alkoxyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline derivatives. Their anticonvulsant activities were evaluated by the MES test and the sc-PTZ test, and their neurotoxicity was evaluated by the rotarod neurotoxicity test with a median toxic dose (TD₅₀) value of 54.5 mg/kg, MES and sc-PTZ tests showed that compound 1 (Table 1) was the most potent of this series with an effective dose (ED₅₀) value of 11.8 and 6.7 mg/kg and protective index (PI = TD₅₀/ED₅₀) value of 4.6 and 8.1, respectively [12].

Table 1. Quinoline anticonvulsant compounds.

Compound No.	R	R1	Reference
1	-H	7-OCH2Ph(4-F)	[12]
2	-Ph	7-OCH2Ph	[13]
3	=O	7-OCH2Ph	[14]
4	=O	8-n-OC6H13	[15]
5	=O	8-n-OC7H15
6	=O	7-n-OC7H15, 2-COC2H5	[16]
7	-H	5-Ph(3-F)	[17]
8	-H	7-n-C6H13, 5-Ph, 4=5	[18]
9	-H	5-n-OC6H13	[19]
10	-CONH2	7-n-OC6H13	[20]
11	5-(1,3,4-triazole), 8-n-OC8H17, 1=2 and 3=4		[21]
12	6-(1,3,4-triazole), 1-n-OC6H13, 2=O		[22]
13	1=2 and 3=4, 8-OCH2Ph,		[23]
14	1=2 and 3=4, 8-OCH2Ph,		[24]
15	1=2 and 3=4, 2-Cl,		[25]

Table 1. Quinoline anticonvulsant compounds.

Compound No.	R	R1	Reference
1	-H	7-OCH2Ph(4-F)	[12]
2	-Ph	7-OCH2Ph	[13]
3	=O	7-OCH2Ph	[14]
4	=O	8-n-OC6H13	[15]
5	=O	8-n-OC7H15
6	=O	7-n-OC7H15, 2-COC2H5	[16]
7	-H	5-Ph(3-F)	[17]
8	-H	7-n-C6H13, 5-Ph, 4=5	[18]
9	-H	5-n-OC6H13	[19]
10	-CONH2	7-n-OC6H13	[20]
11	5-(1,3,4-triazole), 8-n-OC8H17, 1=2 and 3=4		[21]
12	6-(1,3,4-triazole), 1-n-OC6H13, 2=O		[22]
13	1=2 and 3=4, 8-OCH2Ph,		[23]
14	1=2 and 3=4, 8-OCH2Ph,		[24]
15	1=2 and 3=4, 2-Cl,		[25]

Cui et al., reported a synthesis of 1-substituted-7-benzyloxy-4,5-dihydro-[1,2,4]triazolo[4,3-a]-quinolines. Anticonvulsant activity was evaluated in the MES test, sc-Met test, and rotarod neurotoxicity test. The safest compound was 2 (Table 1), with TD₅₀ values of greater than 300 mg/kg which was better than most of the market drugs [13].

Jin et al., prepared a novel type of 7-hydroxyl-3,4-dihydro-2(1H)-quinolines. In the anti-MES test, compound 3 showed ED₅₀ of 12.3 mg/kg (Table 1), TD₅₀ of 547.5 mg/kg, and the PI of 44.5 which was much greater than the PI of the reference drugs phenytoin, phenobarbital, carbamazepin and valproate [14]. Sun et al., reported the synthesis of 8-alkoxy-4,5-dihydro-[1,2,4]triazole[4,3-a]quinoline-l-one derivatives and evaluated their anticonvulsant activities by MES test, sc-PTZ test, and rotarod test. The results demonstrated that compound 4 and compound 5 were the most potent anticonvulsants (Table 1), with ED₅₀ values of 17.17 mg/kg and 24.55 mg/kg and PI values of 41.9 and 29.3 of compound 4 in the MES and sc-PTZ tests, respectively, and compound 5 having ED₅₀ values of 19.7 mg/kg and 21.2 mg/kg and PI values of 36.5 and 33.9 in the MES and sc-PTZ tests, respectively. The PI values of compounds 4 and 5 were many folds better than that of the reference drugs which mentioned above, which have PI values in the range of 1.6–8.1 in the MES test and <0.22–5.2 in the sc-PTZ test [15].

Wei et al., synthesized a series of 2-substituted-7-heptyloxy-4,5-dihydro-[1,2,4]triazolo[4,3-a]-quinolin-1(2H)-ones and evaluated their anticonvulsant activities. Pharmacological tests showed that compound 6 was the most active and also had the lowest toxicity (Table 1). In the anti-MES test, it showed ED₅₀ of 8.2 mg/kg, TD₅₀ of 318.3 mg/kg, and PI of 39.0 which was much greater than the PI of the reference drugs phenytoin and carbamazepine [16].

Guan et al., designed and synthesized a new series of substituted quinoline-2(1H)-one and 1,2,4-triazolo[4,3-a]quinoline derivatives. Their anticonvulsant activities were evaluated by MES test, sc-PTZ test and rotarod test. Compound 7 showed the strongest anticonvulsant effect with ED₅₀ of 27.4 mg/kg and 22.0 mg/kg in the anti-MES and anti-PTZ test, respectively (Table 1) [17].

Guan et al., reported the synthesis of a series of novel 5-phenyl-[1,2,4]triazolo[4,3-a]quinoline derivatives and evaluated their anticonvulsant activities. The MES test showed that compound 8 was found to be the most potent compound with an ED₅₀ value of 6.5 mg/kg and a PI value of 35.1 which was much higher than the PI of the reference drug phenytoin (Table 1) [18].

Guo et al., synthesized a series of 5-alkoxy-[1,2,4]triazolo[4,3-a]quinoline derivatives. Their anticonvulsant activities were evaluated by MES test and their neurotoxicity was measured by the rotarod test. The results demonstrated that compound 9 was the most potent anticonvulsant (Table 1), with ED₅₀ of 19.0 mg/kg and PI value of 5.8 in the MES test [19].

Sun et al., synthesized a series of 8-alkoxy-5,6-dihydro-[1,2,4]triazino[4,3-a]quinolin-1-one derivatives and evaluated their activities. The results showed that compound 10 was the most potent with an ED₅₀ value of 11.4 mg/kg (Table 1), TD₅₀ of 114.1 mg/kg, PI value of 10.0 which is much greater than the PI of the reference drug carbamazepine [20].

Wei et al., established a series of 1-formamidotriazolo[4,3-a]quinoline derivatives and evaluated their anticonvulsant activities. Compound 11 showed an ED₅₀ of 30.1 mg/kg (Table 1), TD₅₀ of 286 mg/kg, and PI of 9.5 which is greater than the reference drug carbamazepine with the PI value of 6.0 [21].

Wang et al., synthesized two series of 8-alkoxy-5-(4H-1,2,4-triazol-4-yl)quinolines and 8-alkoxy-5-(2H-1,2,4-triazol-3-one-4-yl)quinolines. The anticonvulsant activities of these compounds were evaluated with MES test and rotarod test. Among the synthesized compounds, compound 12 was the most active, with and ED₅₀ of 8.80 mg/kg (Table 1), TD₅₀ of 176.03 mg/kg and PI value of 20.0. Its neurotoxicity was the lowest among the synthesized compounds. Meanwhile, it was also significantly lower than carbamazepine that used as reference. Beyond that, the broad spectrum activity of compound 12 was inferred from the anti-seizure results of bicuculline-, PTZ- and 3-mercaptopropionic acid-induced seizure tests [22].

Deng et al., reported the synthesis of a series of 1-substituted-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydroquinolin-2(1H)-ones and screened their anticonvulsant activities. In the MES screening, compound 13 showed anticonvulsant activity in moderation (Table 1). At the dose of 100 mg/kg, all the animals were protected from seizure after treatment with compound 13, and all compounds synthesized exhibited no neurotoxicity [23].

He et al., synthesized 16 new 1-(2-(8-(benzyloxy)quinolin-2-yl)-1-butyrylcyclopropyl)-3-substituted urea derivatives and tested their anticonvulsant activity using the MES test and sc-PTZ screening. The most active compound 14 showed anti-MES activity with an ED₅₀ value of 14.3 mg/kg and TD₅₀ value of 434 mg/kg after i.p. injection to mice (Table 1), which showed compound 14 with a PI of 30.3 in the MES test [24].

He et al., prepared series of 16 new1-(8-(benzyloxy)quinolin-2-yl-6-substituted-4,6-dia-zaspiro [2,4]heptane-5,7-diones and evaluated their anticonvulsant activities using the MES and sc-PTZ tests. The most active compound 15 showed the MES-induced seizures with ED₅₀ value of 8.6 mg/kg and TD₅₀ value of 365.3 mg/kg after i.p. to mice (Table 1), compound 15 with a PI value of 26.8 in the MES test [25].

Kumar et al., demonstrated synthesis of a series of quinoline-incorporated substituted thiadiazole and evaluated their anticonvulsant activity. Compound 16 showed protection against the MES model at 30 mg/kg and showed activity at both 0.5 and 4 h period at dose level of 30 mg/kg indicating the compound to be highly potent and long acting (Table 1) [26].

3. The Quinazoline or Quinazolinone Functional Groups

As new horizons in anticonvulsant therapy, the quinazolines and quinazolinone structural class has been proved to be useful for the design and development of potent anticonvulsant agents [27,28].

Wang et al., synthesized several series of novel 5-alkoxytetrazolo[1,5-a]quinazoline derivatives. Anticonvulsant activities were evaluated using the MES test. Compound 17 protected completely against MES-induced seizure at a dose of 100 mg/kg (Table 2), and was the best active compound in this series [29].

Zheng et al., prepared a series of novel 5-phenyl-[1,2,4]triazolo[4,3-c]quinazolin-3-amine derivatives and screened their anticonvulsant activities by the MES test and their neurotoxicity was evaluated by the rotarod neurotoxicity test. The most promising compound was 18 (Table 2), which showed an ED₅₀ value of 27.4 mg/kg and a PI value of 5.8. These values were superior to those provided by valproate (ED₅₀ and PI values of 272 and 1.6, respectively) in the MES test in mice [30].

El-Azab et al., established a new series of 2,3,8-trisubstituted-4 (3H)-quinazoline derivatives. Compounds 19, 20 and 21 displayed median LD₅₀ values of 1000, 418 and 501 mg/kg with therapeutic index (LD₅₀/ED₅₀) values 10.2, 1.53 and 3.34 (Table 2). Compounds 19, 20 and 21 showed better anticonvulsant activity and much lower toxicity comparable with the reference drugs valproate and methaqualone [31].

El-Azab et al., reported a novel series of 7-substituted-4(3H)-quinazolinone and evaluated their antitumor and anticonvulsant activities. Compounds 22, 23, 24, 25, 26 and 27 showed advanced anticonvulsant activity as well as lower neurotoxicity than reference drugs valproate and methaqualone (Table 2) [32].

Abbas et al., designed and synthesized a series of 2,3-disubstituted quinazolinone derivatives and a [1,2,4]triazino[2,3-c]quinazolinone and screened their anticonvulsant activity using the sc-PTZ and MES models. The study showed the most active compound 28 had a protective dose 50 (PD₅₀) of 200.53 μmol/kg (PD₅₀ of phenobarbitone = 62.18 μmol/kg) (Table 2) [33].

Rajasekaran et al., synthesized a series of ten novel derivatives of 3-substituted-2-thioxoquinazolin-4(3H)-ones. The titled compounds were evaluated for anticonvulsant activities by MES test. The compounds 29 and 30 showed potent anticonvulsant activity (Table 2) [34].

Prashanth et al., reported a novel class of N-substituted glycosmicine derivatives and evaluated their anticonvulsant activity by MES test and their neurotoxic effects were determined by rotorod test in mice. The most active compounds 31 and 32 exhibited anticonvulsant activity against MES-induced seizure at the dose of 100 mg/kg (Table 2). Among all compouds 31 and 32 were recorded 70% of protection [35].

Malik et al., prepared various N-(benzo[d]thiazol-2-ylcarbamoyl)-2-methyl-4-oxoquinazoline-3(4H)-carbothioamide derivatives and evaluated their anticonvulsant activity with MES and sc-PTZ models in mice. The most active one was compound 33 with ED₅₀ value of 82.5 mmol/kg (MES) and 510.5 mmol/kg (sc-PTZ) (Table 2). This molecule was more potent than phenytoin and ethosuximide which were used as reference antiepileptic drugs [36].

Saravanan et al., demonstrated some novel quinazolinone derivatives and screened their antiepileptic activity using MES and sc-PTZ seizure tests. The most active one was compound 34 that revealed protection in MES at a dose of 30 mg/kg (ip) after 0.5 and 4 h (Table 2). This molecule also provided protection in the sc-PTZ at a dose of 100 mg/kg (0.5 h) and 300 mg/kg (4 h) [37].

Table 2. Anticonvulsant activity of quinazoline or quinazolinone compounds.

Compound No.	Substituent Group	Reference No.
19	2-CH3, 3-PH(2-CH3), 8-OCHCONHNH2	[31]
20	2-CH3, 3-PH(2-CH3), 8-OCHCONHNHCOOC2H5
21	2-CH3, 3-PH(2-CH3), 8-OCHCONHNHCSSCH3
22	2-CH3, 3-PH(2-CH3), 8-NHCOOC2H5	[32]
23	2-CH3, 3-PH(2-CH3), 8-NHCHPh(4-F)
24	2-CH3, 3-PH(2-CH3), 8-NHCHPh(4-Cl)
25	2-CH3, 3-PH(2-CH3),
26	2-CH3, 3-PH(2-CH3),
27	2-CH3, 3-PH(2-CH3),
28	2-CH2OPh(2,4-Cl2), 3-NHCOCH2NHNHCOC5H4N	[33]
29	3-Ph, 2-=S, (R=1,3-dichlorobenzene)	[34]
30	3-naphthalene, 2-=S,
31	1-CH3, 2-=O, 3-COC2H4NHPh(4-Cl)	[35]
32	1-CH3, 2-=O, 3-COC2H4NHPh(4-F)
33	2-CH3,	[36]
34	2-CH3,	[37]

Table 2. Anticonvulsant activity of quinazoline or quinazolinone compounds.

Compound No.	Substituent Group	Reference No.
19	2-CH3, 3-PH(2-CH3), 8-OCHCONHNH2	[31]
20	2-CH3, 3-PH(2-CH3), 8-OCHCONHNHCOOC2H5
21	2-CH3, 3-PH(2-CH3), 8-OCHCONHNHCSSCH3
22	2-CH3, 3-PH(2-CH3), 8-NHCOOC2H5	[32]
23	2-CH3, 3-PH(2-CH3), 8-NHCHPh(4-F)
24	2-CH3, 3-PH(2-CH3), 8-NHCHPh(4-Cl)
25	2-CH3, 3-PH(2-CH3),
26	2-CH3, 3-PH(2-CH3),
27	2-CH3, 3-PH(2-CH3),
28	2-CH2OPh(2,4-Cl2), 3-NHCOCH2NHNHCOC5H4N	[33]
29	3-Ph, 2-=S, (R=1,3-dichlorobenzene)	[34]
30	3-naphthalene, 2-=S,
31	1-CH3, 2-=O, 3-COC2H4NHPh(4-Cl)	[35]
32	1-CH3, 2-=O, 3-COC2H4NHPh(4-F)
33	2-CH3,	[36]
34	2-CH3,	[37]

4. The Thiazole or Benzothiazole Functional Groups

In the past few decades, the literature has been enriched with progressive findings about the anticonvulsant activities of various substituted thiazole derivatives [38,39].

Siddiqui et al., prepared a series of 1,3-benzothiazol-2-yl-semicarbazones and evaluated their anticonvulsant activity. Compounds 35, 36 and 37 had shown 100% protection at both the time intervals, that is, 0.5 and 4 h (Table 3). None of the compounds had shown the sign of neurotoxicity [40].

Table 3. Anticonvulsant thiazole or benzothiazole compounds.

Compound No.	R	R1	Reference
35		6-CH3	[40]
36		6-OCH3
37
38		6-F	[41]
39		6-CH3
40		6-Br
41		6-OCH3	[42]
42		5,6-Cl2	[43]
43
44		6-Cl	[44]
45

Table 3. Anticonvulsant thiazole or benzothiazole compounds.

Compound No.	R	R1	Reference
35		6-CH3	[40]
36		6-OCH3
37
38		6-F	[41]
39		6-CH3
40		6-Br
41		6-OCH3	[42]
42		5,6-Cl2	[43]
43
44		6-Cl	[44]
45

Rana et al., prepared a series of 1,3-benzothiazol-2-yl-benzamides and evaluated their anticonvulsant activity. Compounds 38, 39, 40 emerged as anticonvulsants with no neurotoxicity and can be claimed to detect compounds possessing effects against generalized toniceclonic (grand mal) and generalized absence (petit mal) seizures, respectively (Table 3) [41].

Hassan et al., had reported synthesis of a series of N-(substituted benzothiazol-2-yl)amide derivatives and evaluated their anticonvulsant effect. Compound 41 emerged as the most effective, with median doses of 40.96 mg/kg (MES ED₅₀), 85.16 mg/kg (sc-PTZ ED₅₀) and 347.6 mg/kg (TD₅₀) (Table 3) [42].

Siddiqui et al., demonstrated a synthesis of various N-(5-chloro-6-substituted-benzothiazol-2-yl)-N′-(substituted phenyl)-[1,3,4]thiadiazole-2,5-diamines. All the newly synthesized compounds were screened for their anticonvulsant activity and were compared with the standard drug phenytoin sodium. Compounds 42 and 43 showed complete protection against MES-induced seizures (Table 3) [43].

Siddiqui et al., also synthesized a series of sulphonamide derivatives and evaluated their possible anticonvulsant activity and neurotoxicity. Compounds 44 and 45 were active at lower doses of 100 and 30 mg/kg, respectively, after 4.0 h (Table 3). Compounds 44 and 45 showed activity at 300 mg/kg after 4 h in sc-PTZ screening. Two compounds 44 and 45 showed delayed toxicity that was toxic only after 4.0 h, which were comparable with that of Carbamazepine (300 mg/kg) [44].

Farag et al., reported many derivatives of heterocyclic compounds containing a sulfonamide thiazole moiety and evaluated the anticonvulsant effect. Compound 46 obviously showed anticonvulsant activity with no tonic stretching stage and protected all the animals tested (Figure 1) [45].

Figure 1. Structures of compounds 46–55.

Figure 1. Structures of compounds 46–55.

Siddiqui et al., designed and synthesized several heteroaryl semicarbazones. All synthesized compounds were tested for anticonvulsant activity utilizing pentylenetetrazole-induced seizure (PTZ) and MES tests. Three compounds of the series, 47, 48 and 49, exhibited significant anticonvulsant activity at dose of 30 mg/kg comparable to the standard drug phenytoin (Figure 1) [46].

Liu et al., established a new series of 7-alkoxy[1,2,4]triazolo[3,4-b]benzothiazol-3(2H)-ones and evaluated their anticonvulsant activities. Compound 50 was the most active in MES-induced seizure test with ED₅₀ value of 13.6 mg/kg (Figure 1). Meanwhile, its neurotoxicity was extremely low, with PI > 51 [47].

Deng et al., reported synthesis of 7-alkoxy-triazolo-[3,4-b]benzo[d]thiazoles. In the MES test, most of the compounds synthesized showed good effects on convulsion. Among the compounds studied, compound 51 was found to be the most potent compound with ED₅₀ value of 8.0 mg/kg and PI value of 15.0 (Figure 1), possessing better anticonvulsant activity and higher safety than market drugs carbamazepine and phenytoin. Compound 51 exhibited activities of broad spectrum in several animal models [48].

Siddiqui et al., synthesized a number of new 8-substituted-4-(2/4-substituted phenyl)-2H-[1,3,5]triazino[2,1-b][1,3]benzothiazole-2-thiones and evaluated their anticonvulsant in a mouse seizure model and were comparable with the standard drug phenytoin. Compounds 52, 53, 54 and 55 showed complete protection after time periods of 0.5 h and 4 h (Figure 1) [49].

5. The Benzothiazines or Benzoxazinone Functional Groups

Zhang et al., synthesized a novel series of 7-alkoxy-2H-1,4-benzothiazin-3(4H)-ones and a new series of 7-alkoxy-4H-[1,2,4]triazolo[4,3-d]benzo[b][1,4]thiazine derivatives. The anticonvulsant activity of these compounds was evaluated by MES test and tarod test following intraperitoneal injection in KunMing mice. Compound 56 was the most active compound, with an ED₅₀ of 17.0 mg/kg, TD₅₀ of 243.9 mg/kg and PI of 14.3 (Figure 2). The neurotoxicity was the lowest among the synthesized compounds. Meanwhile, it was also significantly lower than carbamazepine that was used as reference. [50].

Siddiqui et al., reported a series of (Z)-2-(substituted aryl)-N-(3-oxo-4-(substituted carbamothioyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-7-yl)hydrazine carboxamides. The anti-convulsant activity was assessed by the MES test, sc-PTZ test and intraperitoneal thiosemicarbazide test (i.p. TSC). Compounds 57, 58, 59 and 60 were the most active ones, protecting 83%–100% of the animals against MES-induced seizures (Figure 2), and also exhibited potent anticonvulsant activity in chemical-induced seizures [51].

Piao et al., prepared a series of 7-benzylamino-2H-1,4-benzoxazin-3(4H)-ones. Their anticonvulsant activities were evaluated by the MES test and their neurotoxicity was evaluated by the rotarod neurotoxicity test. The MES test showed that compound 61 was the most potent with ED₅₀ value of 31.7 mg/kg and PI value of 7.2 (Figure 2) [52].

Figure 2. Structures of compounds 56–61.

Figure 2. Structures of compounds 56–61.

6. The Oxadiazole or Benzoxazinone Functional Groups

The oxadiazole scaffold is very versatile and has been subjected to extensive study in recent years. Compounds containing oxadiazole rings have been studied for many biological activities [53].

Bhat et al., prepared a series of 3-(4-acetyl-5H/methyl-5-substituted phenyl-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2H-chromene-2-ones and evaluated their anticonvulsant activity and neurotoxicity. Compound 62 was found to be potent and had activity at a lower dose of 30 mg/kg in MES-test (Table 4). All the compounds were less toxic as compared with the standard drug phenytoin [54].

Tabatabai et al., synthesized a series of some derivatives of 2-(2-phenoxy)phenyl-1,3,4-oxadiazole. Although the most effective compound 63 was a weaker anticonvulsant than diazepam (Table 4), it should be mentioned that it had a good margin of safety and LD₅₀, which were 15-fold its ED₅₀ [55].

Harish et al., reported a series of novel 1-[5-(4-methoxyphenyl)-[1,3,4]oxadiazol-2-yl]-piperazine derivatives. The anticonvulsant effects of these derivatives on MES-induced seizures were experimented in male Wistar rats and phenytoin was used as reference drug. Compounds 64, 65, 66 and 67 showed excellent anticonvulsant activity in MES model (Table 4) [56].

Table 4. Anticonvulsant oxadiazole or benzoxazinone compounds.

Compound No.	R	R1	Reference
64		4-OCH3	[56]
65		4-OCH3
66		4-OCH3
67		4-OCH3
68			[57]
69
70

Table 4. Anticonvulsant oxadiazole or benzoxazinone compounds.

Compound No.	R	R1	Reference
64		4-OCH3	[56]
65		4-OCH3
66		4-OCH3
67		4-OCH3
68			[57]
69
70

Harish et al., investigated a series of new 2-methyl-2-[3-(5-piperazin-1-yl-[1,3,4]oxadiazol-2-yl)-phenyl]-propionitrile derivatives. All the compounds were screened for their anticonvulsant activity against MES seizure and their neurotoxic effects were determined by rotorod test. Compounds 68, 69 and 70 were found to be the most potent of this series (Table 4). These compounds showed no neurotoxicity at the maximum dose administered (100 mg/kg) [57].

Siddiqui et al., reported a synthesis of new 5-(1H-indol-3-yl)methyl-4-(substituted-aryl)-2,4-dihydro-3H-1,2,4-triazole-3-thiones. All the newly synthesized compounds were screened for their anticonvulsant activity in the MES model and were compared with the standard drugs phenytoin sodium and carbamazepine. Among these compounds, 71 was found to be the most active in the series that showed protection against seizures both after 0.5 h and 4 h at 30 mg/kg body mass (Table 4) [58].

Siddiqui et al., designed and synthesized a series of 5-carbomethoxybenzoxazole derivatives. Compounds 72, 73, 74 and 75 were found to be more lipophilic (Figure 3), thus having potent anticonvulsant activity [59].

Wei et al., demonstrated a synthesis of novel 2-substituted-6-(4H-1,2,4-triazol-4-yl)benzo[d] oxazoles and evaluated the anticonvulsant activity with the MES test and sc-PTZ test. Compound 76 was the most active and also had the lowest toxicity (Figure 3). In the anti-MES potency test, it showed ED₅₀ of 29.5 mg/kg, a TD₅₀ of 285 mg/kg, and a PI of 9.7 which was greater than the reference drug, carbamazepine that has a PI of 6.4 [60].

Figure 3. Structures of compounds 71–79.

Figure 3. Structures of compounds 71–79.

Malik et al., prepared a series of 3-(benzo[d]isoxazol-3-yl)-N-substituted pyrrolidine-2,5-dione and evaluated their anticonvulsant activities. Preliminary anticonvulsant activity was performed using MES and sc-PTZ tests after ip injection into mice. ED₅₀ value of compound 77 was 14.90 mg/kg (Figure 3). Similarly the most potent one in sc-PTZ was compound 78 with an ED₅₀ value of 42.30 mg/kg (Figure 3). These compounds were more active and had lower neurotoxicity than the control drugs ethosuximide and phenytoin [61].

Malik et al., synthesized a novel series of (5-amino-3-substituted-1,2,4-triazin-6-yl)(2-(6-halo-substituted-benzo[d]isoxazol-3-yl) pyrrolidin-1-yl)methanone. The MES test showed that compound 79 was the most potent compound (Figure 3), with an ED₅₀ value of 6.20 mg/kg (oral/rat) and a PI value of >48.38 which was much higher than the PI of the reference drug phenytoin [62].

7. The Pyridine Functional Group

Pyridines and substituted pyridines are an important family of heterocyclic compounds that has attracted significant interest in medicinal chemistry in recent years [63]. Prasanthi et al., reported synthesis of dialkyl 4-(benzo[d][1,3]dioxol-6-yl)-1,4-dihydro-2,6-dimethyl-1-substituted pyridine-3,5-dicarboxylates. The present study revealed that compound 80 showed promising anticonvulsant activity compared to phenytoin (Figure 4). Further, the prediction data of the molecular properties supports that compound 80 might involve hydrogen bonding interaction with target site, and displayed good binding in silico absorption and lower binding rate of plasma to protein, which made it to be a good candidate for treatment of epilepsy [64].

Prasanthi et al., prepared a series of new N-diethylmalonyl derivatives of nifedipine and other isosteric analogues. Anticonvulsant screening was performed using sc-PTZ and MES induced seizures. The majority of the compounds were effective in sc-PTZ and MES screening. Compound 81 showed good activity displaying the maximum protection (Figure 4) [65].

Guan LP et al., described a series of new 5-alkoxy-[1,2,4]triazolo[4,3-a]pyridine derivatives and evaluated their anticonvulsant activity and neurotoxicity with the MES and rotarod tests, respectively. The most promising compounds, 82 and 83 showed ED₅₀ values of 13.2 and 15.8 mg/kg and had a PI value of 4.8 and 6.9, respectively (Figure 4) [66].

Figure 4. Structures of compounds 80–83.

Figure 4. Structures of compounds 80–83.

8. The Pyrazole Functional Group

Pyrazole and its derivatives consist of five-membered heterocycles with two ortho-nitrogen-atoms. These compounds have received attention in the field of current medicinal and pharmacological research, and are reported to have a broad spectrum of biological activities, such as antitumor, antimicrobial, antioxidant and antimalarial activities [67,68,69,70].

Kaushik et al., established synthesis of N′-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene]2/4-substituted hydrazides and evaluated their anticonvulsant activity against MES- and sc-PTZ-induced seizure models in mice. All compounds showed protection in the MES model at 100 mg/kg, including compound 84 which showed activity at 0.5 h and 4.0 h periods indicating that 84 was potent having a rapid onset and long duration of action (Figure 5). Compound 84 showed activity at a dose of 100 mg/kg comparable to sodium valproate in the sc-PTZ test [71].

Figure 5. Structures of compounds 84–91.

Figure 5. Structures of compounds 84–91.

Siddiqui et al., had reported various 3,5-(substituted-diphenyl)-4,5-dihydro-pyrazole-1-acid phenylamides and evaluated their anticonvulsant activities. Compounds 85, 86, 87 and 88 were found to protect 100% of the animals in the MES screening at a dose of 25 mg/kg (Figure 5). They were also found to have appreciable anticonvulsant activity in sc-PTZ screening [72].

Ahsan MJ et al., designed and synthesized a series of fourteen 3a,4-dihydro-3H-indeno[1,2-c] pyrazole-2-carboxamide/carbothioamide analogues. Among the compounds synthesized, some exhibited marked effect on seizure model under minimal clonicity (6 Hz psychomotor seizure test). Compound 89 was found to be the most active compound of the series showing 75% (3/4, 0.25–2.0 h) and 50% (2/4, 4.0 h) protection against minimal clonic seizure at 100 mg/kg without any toxicity (Figure 5). Compound 90 showed protection in MES seizure and subcutaneous metrazol (sc-MET) seizure at 300 mg/kg (Figure 5) [73].

Farghaly A et al., synthesized a series of new pyrazolo[3,4-b]pyrazines containing, 1,2,4-oxadiazolyl, thiadiazolyl, imidazothiadiazolyl, thiazolidinonyl, substituents and other different substituents. Compound 91 showed best results at reducing PTZ-induced tonic convulsions and mortality (Figure 5) [74].

9. The Imidazole Functional Group

Imidazole and its derivatives are a class of 5-membered heterocyclic structures having two non-adjacent nitrogen atoms. Recent studies revealed that the substituted imidazole derivatives have attracted much attention due to their broad spectrum of pharmacological activities such as anti-inflammatory, analgesic [75,76]. Literature survey shows that imidazole-heterocyclic compounds could be new classes of anticonvulsant agents by the virtue of their potential anticonvulsant properties [77].

Karakurt et al., described a series of 2-acetylnaphthalene derivatives. Quantification of anti-convulsant protection was calculated via the i.p. route (ED₅₀ and TD₅₀) for the most active candidate (92) (Figure 6). Observed protection in the MES model was 38.46 mg/kg and 123.83 mg/kg in mice and 20.44 mg/kg, 56.36 mg/kg in rats, respectively [78].

Figure 6. Structures of compounds 92–94.

Figure 6. Structures of compounds 92–94.

Husain et al., established a synthesis of a series of 1,2,4-trisubstituted-1H-imidazole derivatives. Anticonvulsant activity was shown by the majority of the synthesized compounds in the MES and sc-PTZ screening when given i.p. to mice. In anticonvulsant screening, only one compound, 93, showed potent activity comparable to that of standard drugs phenytoin and carbamazepine (Figure 6) [79].

Amir et al., demonstrated synthesis of a series of novel imidazole incorporated semicarbazones. Compound 94 showed the highest activity among the compounds synthesized with no neurotoxic and depressant effects on CNS (Figure 6). Liver enzyme estimations (serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase) of the compound also showed no significant change in the enzyme levels [80].

Ulloora et al., prepared a variety of five new series of imidazo[1,2-a]pyridines carrying biologically active pyrazoline, cyanopyridone, cyanopyridine, 2-aminopyrimidine and pyrimidine-2-thione systems. The target compounds were screened for their in vivo anticonvulsant activity following MES and sc-PTZ methods at a small test dose of 10 mg/kg. Compounds 95, 96, 97, 98, 99 and 100 displayed potent anticonvulsant activity without displaying any toxicity (Table 5) [81].

Ulloora et al., designed and synthesized new 2-arylimidazo[1,2-a]pyridines carrying suitably substituted 1,2,3-triazoles. The anticonvulsant study was carried out by MES and sc-PTZ screening methods, while their toxicity study was performed following rotarod method. The most active was compound 101 which displayed reasonably good activity in both the durations of 0.5 and 4 h indicating that they possess rapid onset and long duration of action (Table 5). It exhibited complete protection against seizure and their activity at 20 mg/kg was comparable with that of standard drug diazepam [82].

Table 5. Anticonvulsant imidazole compounds.

Compound No.	R	R1	Reference
95		-F	[81]
96
97
98
99		-H
100		-H
101		-CH3	[82]

Table 5. Anticonvulsant imidazole compounds.

Compound No.	R	R1	Reference
95		-F	[81]
96
97
98
99		-H
100		-H
101		-CH3	[82]

10. The Pyrimidine Functional Group

Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines, six-membered heterocyclics with two nitrogen atoms in the ring, has the nitrogens at positions 1 and 3 in the ring. Pyrimidines that have a broad spectrum of bioactivities (antibacteria, anticancer and anti-inflammation and so on) are an important one of the heterocyclic compounds [83,84,85].

Alam et al., synthesized a number of N-(4,6-substituted diphenylpyrimidin-2-yl) semicarbazones and tested their anticonvulsant activity against the two seizure models, MES and sc-PTZ. Three compounds (102, 103 and 104) were found to be significantly active as they showed protection at the lowest dose of 30 mg/kg after 0.5 h and did not show any sign of neurotoxicity except in case of compound 102 which was found to be neurotoxic at 300 mg/kg after 4.0 h (Figure 7) [86].

Deng et al., described the synthesis and anticonvulsant activities of 7-(substituted-phenyl)-6,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-ones and their derivatives. The majority of the compounds synthesized showed inhibition effects on MES-induced convulsion. The most promising compound 105 showed significant anticonvulsant activity in MES test with ED₅₀ value of 19.7 mg/kg (Figure 7). It was safer than reference drugs with much higher PI value. In addition, the protective effect of compound 105 against seizures induced by PTZ, ISO, TSC, 3-MP, and bicuculline in the chemical-induced seizure tests suggested that compound 103 displayed broad spectrum activity in several models [87].

Jiang et al., reported a novel series of 7-substituted-5-phenyl-[1,2,4]triazolo[1,5-a] pyrimidines. Their anticonvulsant activities were measured through the MES test, and carbamazepine (ED₅₀ = 11.8 mg/kg) and valproate (ED₅₀ = 272 mg/kg) were used as the reference drugs. Amongst the compounds tested, compound 106 was the most active in inhibiting convulsion with ED₅₀ value of 84.9 mg/kg that was higher than valproate but lower than carbamazepine (Figure 7) [88].

Shaquiquzzaman et al., established syntheses of some new pyrimidine-5-carbonitrile derivatives. In the MES test, compounds 107, 108 and 109 were found to be highly active at a dose level of 30 mg/kg at 0.5 h time interval (Figure 7), indicating their ability to prevent seizure spread at a relatively low dose [89]. Shaquiquzzaman et al., also reported a series of dihydropyrimidine-5-carbonitrile derivatives and evaluated their anticonvulsant activity against MES and sc-PTZ models. Compounds 110 and 111 were found to be most active showing activity both in MES and sc-PTZ screen at lower doses of 30 mg/kg at 0.5 h and 100 mg/kg at 4 h (Figure 7). In the rotarod motor impairment screen, compound 110 did not show any motor impairment, even at the maximum dose of 300 mg/Kg. The pharmacophore hypothesis also fits best for compounds 110 and 111 [90].

Figure 7. Structures of compounds 102–111.

Figure 7. Structures of compounds 102–111.

11. The Phthalazine Functional Group

As a heterocyclic compound, the molecular formula of phthalazine is C₈H₆N₂. Because of the broad spectrum of bioactivities such as anticonvulsion, vasorelaxation, anti-inflammation and cardiotonic effect, its derivatives are generally used for treating disease [91,92,93].

Zhang et al., designed and synthesized a new series of 6-alkoxy-[1,2,4]triazolo[3,4-a] phthalazines and evaluated their anticonvulsant activity and neurotoxicity by the MES test and the rotarod test respectively. The most promising compounds 112 and 113 showed a median effective dose of 7.1 and 11.0 mg/kg (Figure 8), and had protective index values of 5.2 and 8.0, respectively. The two compounds were further found to have potent activity against seizures induced by PTZ, ISO, TSC, 3-MP but not seizures induced by strychnine [94].

Sun et al., investigated a new phthalazine tetrazole derivative. Compound 114 exhibited higher activity (ED₅₀ = 6.8 mg/kg) and lower neurotoxicity (TD₅₀ = 456.4 mg/kg) (Figure 8), resulting in a higher PI = 67.1 compared with carbamazepine (PI = 6.4). In addition, compound 114 exhibited significant oral anticonvulsant activity (ED₅₀ = 24 mg/kg) against MES-induced seizure with low neurotoxicity (TD₅₀ > 4500 mg/kg) in mice, resulting in a PI value of more than 187.5. Compound 114 was also tested in chemically induced animal models of seizure (PTZ, ISO, TSC and 3-MP) to further investigate the anticonvulsant activity. Compound 114 produced significant anticonvulsant activity against seizures induced by ISO, TSC and 3-MP [95].

Bian et al., reported a synthesis of new 6-substituted-[1,2,4]triazolo[3,4-a](tetrazolo[5,1-a]) phthalazine derivatives. All the compounds were evaluated for their anticonvulsant activities using the MES test. The most promising compound 115 showed significant anticonvulsant activity in MES test with ED₅₀ value of 9.3 mg/kg (Figure 8). It displayed a wide margin of safety with protective index much higher than the standard drug carbamazepine [96].

Figure 8. Structures of compounds 112–115.

Figure 8. Structures of compounds 112–115.

12. The Triazine Functional Group

Triazine is a six membered heterocyclic ring compound containing three nitrogen atoms. The triazine moiety has also attracted the attention of chemists because many triazines are biologically active and are used in medicine, especially as anti-AIDS, anticancer, and antitubercular agents, for their anti-anxiety and anti-inflammatory activities, as well as used in agriculture [97,98,99].

Kaushik et al., designed and synthesized a new series of 2-(substituted aryloxy)-5-(substituted benzylidene)-3-phenyl-2,5-dihydro-1H-[1,2,4]triazin-6-one. Their anticonvulsant activity was evaluated by MES test, sc-PTZ test. Among the compound tested, compound 116 showed protection from seizures in both the animal models at dose level of 30 mg/kg (Figure 9). The compound 116 showed activity both at 0.5 h and 4 h periods at dose level of 30 mg/kg, indicating the compound to be highly potent and long acting [100].

Amir et al., demonstrated synthesis of new hydrazone incorporated triazines and evaluated for their anticonvulsant activity through MES and sc-PTZ screenings. Among the tested compounds, compound 117 (MES ED₅₀ 54.31, sc-PTZ ED₅₀ 92.01) and compound 118 (MES ED₅₀ 46.05, sc-PTZ ED₅₀ 83.90) emerged as the most active anticonvulsant agent having GABA-ergic effects (Figure 9). Compounds 117 and 118 also showed less CNS depressant effect than the standard drug carbamazepine [101].

Ahuja et al., synthesized a series of thirty indole C-3 substituted 5-amino-6-(5-substituted-2-phenyl-1H-indol-1-yl)-4,5-dihydro-1,2,4-triazine-3(2H)-thiones. Compound 119 had significant activity in the MES test with minimal duration of limb extension (5.40 ± 0.61 s) and quantitative median dose of 7 mg/kg. In sc-PTZ screening, compound 120 increased the seizure latency to clonic convulsion and with effective at a median dose of 35 mg/kg (Figure 9) [102].

Figure 9. Structures of compounds 116–120.

Figure 9. Structures of compounds 116–120.

13. The Triazolethione Functional Group

Many compounds bearing a triazole moiety were found to possess anticonvulsant properties in various animal models of epilepsy. Therefore, some people want to loop through a combination of triazole-thione compounds to improve the antiepileptic activity.

Luszczki et al., reported the effects of 4-(4-bromophenyl)-5-(3-chlorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (compound 121) and 5-(3-chlorophenyl)-4-(4-methylphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (compound 122) on the protective action of four classical antiepileptic drugs—carbamazepine, phenobarbital, phenytoin and valproate—against MES test in mice (Table 6). Results indicated that compound 121 administered intraperitoneally at doses of 75 and 100 mg/kg significantly elevated the threshold for electroconvulsions in mice. Compound 121 (50 mg/kg) significantly enhanced the anticonvulsant activity of carbamazepine, phenobarbital and valproate. Compound 122 administered intraperitoneally at 10 mg/kg significantly elevated the threshold for electroconvulsions in mice. Moreover, compound 122 (5 mg/kg) significantly enhanced the anticonvulsant activity of valproate, but not that of carbamazepine, phenobarbital or phenytoin in the MES test in mice. Pharmacokinetic experiments revealed that compound 122 significantly elevated total brain concentrations of valproate in mice [103,104].

Table 6. Structures of compounds 121–126.

Compound No.	R	R1	Reference
121	-Ph(p-Br)	—	[103,104]
122	-Ph(p-CH3)	—
123	n-C6H13	—	[105]
124	-Ph(p-F)	—
125	-Ph(o-CH3)	-Cl	[106]
126	-Ph(p-OCH3)	-Br	[107]

Table 6. Structures of compounds 121–126.

Compound No.	R	R1	Reference
121	-Ph(p-Br)	—	[103,104]
122	-Ph(p-CH3)	—
123	n-C6H13	—	[105]
124	-Ph(p-F)	—
125	-Ph(o-CH3)	-Cl	[106]
126	-Ph(p-OCH3)	-Br	[107]

Siddiqui et al., prepared a various of 3-[4-(substituted phenyl)-1,3-thiazol-2-ylamino]-4-(substituted phenyl)-4,5-dihydro-1H-1,2,4-triazole-5-thiones. Their in vivo anticonvulsant screenings were performed using the two most adopted seizure models, MES and sc-PTZ. Two compounds, 123 and 124 (Table 6), showed significant anticonvulsant activity in both the screenings with ED₅₀ values of 23.9 mg/kg and 13.4 mg/kg, respectively, in the MES screen and 178.6 mg/kg and 81.6 mg/kg, respectively, in the sc-PTZ test. They displayed a wide margin of safety with PI, median hypnotic dose (HD₅₀) and median lethal dose (LD₅₀) which were much higher than that of the standard drugs [105].

Plech et al., designed and synthesized 4-alkyl-1,2,4-triazole-3-thione derivatives. A group of derivatives showed strong anticonvulsant activity. The characteristic features of the most active compounds were rapid onset and long lasting effects. Among the tested compounds, compound 125 was assayed for the different PI values at different preprocessing times (Table 6), and the results of that were ranging from 2.8 to 9.7 [106].

Plech et al., also reported a synthesis of 1,2,4-triazole-3-thione derivatives. Characteristic features of all active compounds were a rapid onset of action and long lasting effects. Compound 126 exhibited the most potent activity (ED₅₀ = 35.2 mg/kg) (Table 6) [107].

14. The Indoline-2,3-dione Functional Group

Isatin (indoline-2,3-dione), one of the simplest indole derivatives, has led to numerous analogues with a wide range of biological properties, including anxiogenic, sedative, anticonvulsant, anticancer activities [108,109].

Siddiqui et al., designed various 1-(amino-N-arylmethanethio)-3-(1-substituted-benzyl-2,3-dioxoindolin-5-yl) ureas. Their in vivo anticonvulsant screenings were performed by the two most adopted seizure models, MES and sc-PTZ. At 300 mg/kg, compounds 127 and 128 showed significant protective effect on MES- and sc-PTZ-induced seizures (Figure 10). Even at the lower dose of 100 mg/kg, compound 128 exhibited good protection on MES-induced seizure. These two compounds exhibited marked protective effect against seizures in a 6 Hz psychomotor seizure test, and could be used as lead compounds for future investigations [110].

Prakash et al., prepared a series of 1-(substituted benzylidene)-4-(1-(morpholino/piperidino methyl)-2,3-dioxoindolin-5-yl) semicarbazides. The compounds were subjected to in vivo antiepileptic evaluation using MES and sc-PTZ test methods. The neurotoxicity was determined by rotarod test. Among the synthesized compounds, 129 revealed excellent protection in both models with lower neurotoxicity (Figure 10) [111].

Figure 10. Structures of compounds 127–129.

Figure 10. Structures of compounds 127–129.

15. The Cyclopropanecarboxylate Functional Group

He et al., synthesized twenty three 1-(2-arylhydrazinecarboxamido)-2,2-dimethylcyclopropane-carboxylate derivatives and tested their anticonvulsant activity using the MES, sc-PTZ screens. Their neurotoxicity was determined by applying the rotorod test. The most active compound 130 showed protection against the MES-induced seizures with ED₅₀ value of 9.8 mg/kg and TD₅₀ value of 332.2 mg/kg after i.p. to mice (Figure 11), which provided compound 128 with a PI of 33.9 in the MES test [112].

Zhong et al., reported fourteen ethyl 2,2-dimethyl-1-(2-substituted-hydrazinecarboxamido) cyclopropanecarboxylate derivatives and tested the anticonvulsant activity using the MES, sc-PTZ screens. The most active compound 131 showed protection against MES-induced seizures with an ED₅₀ value of 9.2 mg/kg and TD₅₀ value of 387.5 mg/kg after i.p. to mice (Figure 11), which provided compound 129 with a PI of 42.1 in the MES test [113].

Figure 11. Structures of compounds 130–131.

Figure 11. Structures of compounds 130–131.

16. The Pyrrolidine-2,5-dione Functional Group

Derivatives of pyrrolidine-2,5-diones, as heterocyclic compounds, have been widely applied in medicinal chemistry and synthesis fields. They exhibit numerous bioactivities, especially in anticonvulsant and tyrosinase inhibitory activities. Therefore, development of new and efficient strategies for the synthesis of multi-substituted pyrrolidine-2,5-diones is also the current hot in organic and medical chemistry [114].

Obniska et al., designed and synthesized many series pyrrolidine-2,5-diones (Table 7) and tested their anticonvulsant activity in the MES and metrazole seizure threshold (sc-Met) tests [115,116,117,118,119,120,121,122,123,124,125,126,127]. The quantitative evaluation in the MES seizures after oral administration into rats showed that the most active were compound 153 with ED₅₀ of 7.4 mg/kg and compound 154 with ED₅₀ of 26.4 mg/kg. These molecules were more potent and also less neuron-toxicity than that of phenytoin which was used as reference antiepileptic drug. Although Kaminski et al., had reported several series pyrrolidine-2,5-diones (Table 7) used for anticonvulsant activity, none exhibited better than compound 153 [128,129,130,131,132].

Table 7. Structures of compounds 132–165.

Comp. No.	R	R1	R2	X	Reference
135	-NHPh(p-CH3)		—	—	[116,117,118]
136	-NHPh(o-CF3)
137	-NHPh
138	-NHPh(2,4-Cl2)
139	-NHPh(m-CH3)				[116]
140	-NHPh(2,4-Cl2)				[117]
141	-Ph(o-OCH3)				[119]
142	-NHPh(4-Cl)
143					[120]
144
145	-NHPh				[121]
146					[122]
147		-Ph(o-CF3)			[123]
148	-N(C2H4)2N-CH3	-Ph(m-Cl)			[124]
149					[125]
150	-Ph(m-CF3)	-H	-Ph(m-CH3)	N	[126,127,128]
151	-Ph(p-Cl)	-H	-Ph(m-Cl)
152	-Ph(m-CF3)	-H	-Ph(m-Cl)
153	-Ph(p-F)	-H	-Ph(o-Br)
154	-Ph(m-Cl)	-H	-Ph(o-Br)
155	-Ph	-H	-Ph(m-CF3)		[123,124,125,126,127,128]
156	-CH2Ph	-H	-Ph(o-Cl)	C
157	—	-H	-Ph	O	[129]
158	-CH2CH2OH	-CH3		N	[130]
159	-CH2Ph			C
160	-Ph(p-F)			N	[131]
161	-Ph(m-Cl)
162	-Ph(3,4-Cl2)
163	-Ph(m-CF3)	-Ph	-Ph		[132]
164	-Ph(3,4-Cl2)	-H	-CH3		[133]
165	-Ph(3,4-Cl2)	-H	-H

Table 7. Structures of compounds 132–165.

Comp. No.	R	R1	R2	X	Reference
135	-NHPh(p-CH3)		—	—	[116,117,118]
136	-NHPh(o-CF3)
137	-NHPh
138	-NHPh(2,4-Cl2)
139	-NHPh(m-CH3)				[116]
140	-NHPh(2,4-Cl2)				[117]
141	-Ph(o-OCH3)				[119]
142	-NHPh(4-Cl)
143					[120]
144
145	-NHPh				[121]
146					[122]
147		-Ph(o-CF3)			[123]
148	-N(C2H4)2N-CH3	-Ph(m-Cl)			[124]
149					[125]
150	-Ph(m-CF3)	-H	-Ph(m-CH3)	N	[126,127,128]
151	-Ph(p-Cl)	-H	-Ph(m-Cl)
152	-Ph(m-CF3)	-H	-Ph(m-Cl)
153	-Ph(p-F)	-H	-Ph(o-Br)
154	-Ph(m-Cl)	-H	-Ph(o-Br)
155	-Ph	-H	-Ph(m-CF3)		[123,124,125,126,127,128]
156	-CH2Ph	-H	-Ph(o-Cl)	C
157	—	-H	-Ph	O	[129]
158	-CH2CH2OH	-CH3		N	[130]
159	-CH2Ph			C
160	-Ph(p-F)			N	[131]
161	-Ph(m-Cl)
162	-Ph(3,4-Cl2)
163	-Ph(m-CF3)	-Ph	-Ph		[132]
164	-Ph(3,4-Cl2)	-H	-CH3		[133]
165	-Ph(3,4-Cl2)	-H	-H

Rybka et al., reported a synthesis of 22 new N-[(4-phenylpiperazin-1-yl)-methyl]-3-methyl-pyrrolidine-2,5-dione and pyrrolidine-2,5-dione derivatives. Administration to mice revealed that the most active compounds were compound 164 with ED₅₀ = 16.13 mg/kg (MES), ED₅₀ = 133.99 mg/kg (sc-PTZ) and compound 165 with ED₅₀ = 37.79 mg/kg (MES), ED₅₀ = 128.82 mg/kg (sc-PTZ) (Table 7). Compared with the positive control drugs valproate and ethosuximide, these compounds exhibited more activity and less neurotoxicity [133].

17. The Imidazoline-2,4-dione Functional Group

Imidazoline-2,4-diones, also called hydantoins, a class of cyclic imides, have been demonstrated to possess good anticonvulsant properties [134]. Their substitution products have also been found a number of other pharmacological properties such as antitumor, anti-HIV and antibacterial activities [135,136,137].

He et al., synthesized new 6-methyl-1-substituted-4,6-diazaspiro[2.4]heptane-5,7-diones and tested the anticonvulsant activity using the MES and sc-PTZ screens. Their neurotoxicity was determined by the rotarod test. The most active of the series was compound 166 (Table 8), which showed a MES ED₅₀ value of 12.5 mg/kg in mice. The TD₅₀ was 310 mg/kg, providing compound 166 with a PI of 24.8 in the MES test which is better than that of Phenytoin [138].

He et al., investigated some new N-3-arylamide substituted 5,5-cyclopropanespirohydantoin derivatives synthesized and tested for anticonvulsant activity using the maximal electroshock (MES), subcutaneous pentylenetetrazole (sc-PTZ) screens, which are the most widely employed seizure models for early identification of candidate anticonvulsants. Their neurotoxicity was determined applying the rotorod test. The most active compound 167 showed the MES-induced seizures with ED₅₀ value of 9.2 mg/kg and TD₅₀ value of 421.6 mg/kg after i.p. to mice (Table 8), which provided compound 167 with a protective index (TD₅₀/ED₅₀) of 45.8 in the MES test [139].

Botros et al., designed and synthesized new phenytoin derivatives and tested the anticonvulsant activity. Preliminary anticonvulsant screening was performed using standard MES and sc-PTZ screens in mice. The neurotoxicity was determined by applying the rotarod test. Among these compounds, 168 and 169 showed the highest protection (80%) in the sc-PTZ test at a dose of 100 mg/kg, whereas the compound 170 displayed promising anticonvulsant effect in the MES model (Table 8) [140].

Byrtus et al., prepared a various of N-Mannich bases derived from 5-cyclopropyl-5-phenyl- and 5-cyclopropyl-5-(4-chlorophenyl)-imidazolidine-2,4-diones. The quantitative evaluation after oral administration in rats showed that the most active was compound 171 with ED₅₀ values of 5.76 mg/kg (MES) and 57.31 mg/kg (sc-PTZ) (Table 8). Compared with the control drugs of ethosuximide and phenytoin, it was more active in the anti-convulsion assays. Additionally compound 171 with ED₅₀ of 26.06 mg/kg in a psychomotor seizure test (6-Hz) in mice showed comparable activity to a new generation anticonvulsant-levetiracetam [141].

Dhanawat et al., had reported a synthesis of N-(3)-substituted-2,4-imidazolidine diones and oxazolidinediones derivatives and tested the anticonvulsant activity using the MES test. Compounds 172, 173, 174 and 175 exhibited significant anticonvulsant activity as compared to the standard drug phenytoin (Table 8) [142].

Botros et al., described new bivalent ligands derived from phenytoin. Initial anticonvulsant screening was performed using MES and PTZ screens in mice. Most of the test compounds were found to be effective in at least one seizure model at a dose of 100 mg/kg. Compound 176 exhibited marked anticonvulsant activity in both MES and PTZ screens (Table 8) [143].

Byrtus et al., established a synthesis of N-Mannich from 5-cyclopropyl-5-phenyl- and 5-cyclopropyl-5-(4-chlorophenyl)-hydantoins and tested their anticonvulsant activity. The quantitative studies after oral administration to rats showed that several molecules were more potent than phenytoin and ethosuximide which were used as reference antiepileptic drugs. From the whole series, the most active was compound 177 with the ED₅₀ value of 5.29 mg/kg in the MES test (Table 8) [144].

Madaiah et al., demonstrated a synthesis of new 3-[(2,4-dioxo-1,3,8-triazaspiro[4,6]undec-3-yl) methyl]benzonitrile derivatives and evaluated their possible anticonvulsant activity by MES and PTZ tests. Compounds 178, 179, 180 and 181 showed significant and protective effect on seizure when compared with the standard drug valproate (Table 8). These compounds were found to exhibit advanced anticonvulsant activity as well as lower neurotoxicity than the reference drug [145].

Madaiah et al., synthesized a series of novel 1′-[2-(difluoromethoxy)benzyl]-2′H,5′H-spiro[8-azabicyclo[3,2,1]octane-3,4′-imidazolidine]-2′,5′-dione substituted hydantoins. The novel molecules were screened for anticonvulsant activity in mice by MES and sc-PTZ-induced seizure tests. The neurotoxicity was assessed using the rotarod method. Compounds 182, 183, 184, 185 and 186 exhibited anticonvulsant potency against MES-induced seizure and in the sc-PTZ model (Table 8), with lesser neurotoxicity. Some title compounds showed lesser depression on central nervous system compared to phenytoin [146].

Table 8. Structures of compounds 166–186.

Comp. No.	R	R1	R2	Reference
166	-CH3	H	-Ph(p-SO2CH3)	[138]
167	-NHCOPh(p-CF3)	-CH3	-CH3	[139]
168	-CH2C(O)NNCSH	-Ph	-Ph	[140]
169	-CH2CONHNHCSNHPh(p-OCH3)	-Ph	-Ph
170	-CH2CONHNHCSNHPh	-Ph	-Ph
171	-H	-Ph	-C3H5	[141]
172	-CH2N(CH2CH2)2Ph	-Ph	-C3H5	[142]
173	-CH2CONHPh(p-Cl)	-Ph	-Ph
174	-CH2CONHPh(o-Cl)	-Ph	-Ph
175	-CH2CONHPh(p-OCH3)	-Ph	-Ph
176	-CH2CON(CH2CH2)2Ph(p-NO2)	-Ph	-Ph	[143]
177	-(CH2)2O(CH2)2 N(CH2CH2)2Ph(p-Cl)	-Ph	-Ph	[144]
178	-SO2Ph(o-F)	—	—	[145]
179	-SO2Ph(m-F)
180	-CO Ph(m-F)
181	-CO Ph(p-F)
182	-SO2Ph(o-F)			[146]
183	-SO2Ph(m-F)
184	-SO2Ph(o-F)
185	-CONHPh
186	-CONHPh(m-CH3)

Table 8. Structures of compounds 166–186.

Comp. No.	R	R1	R2	Reference
166	-CH3	H	-Ph(p-SO2CH3)	[138]
167	-NHCOPh(p-CF3)	-CH3	-CH3	[139]
168	-CH2C(O)NNCSH	-Ph	-Ph	[140]
169	-CH2CONHNHCSNHPh(p-OCH3)	-Ph	-Ph
170	-CH2CONHNHCSNHPh	-Ph	-Ph
171	-H	-Ph	-C3H5	[141]
172	-CH2N(CH2CH2)2Ph	-Ph	-C3H5	[142]
173	-CH2CONHPh(p-Cl)	-Ph	-Ph
174	-CH2CONHPh(o-Cl)	-Ph	-Ph
175	-CH2CONHPh(p-OCH3)	-Ph	-Ph
176	-CH2CON(CH2CH2)2Ph(p-NO2)	-Ph	-Ph	[143]
177	-(CH2)2O(CH2)2 N(CH2CH2)2Ph(p-Cl)	-Ph	-Ph	[144]
178	-SO2Ph(o-F)	—	—	[145]
179	-SO2Ph(m-F)
180	-CO Ph(m-F)
181	-CO Ph(p-F)
182	-SO2Ph(o-F)			[146]
183	-SO2Ph(m-F)
184	-SO2Ph(o-F)
185	-CONHPh
186	-CONHPh(m-CH3)

18. The Oxime Ether Functional Group

Due to the lipophilic aryl portion facilitating penetration of the blood–brain barrier, the introduction of oxime ether groups to the compounds as a small oxygen functional group had been studied. Meanwhile, oxime ether linkages also are used as a mechanism for pro-drug generation [147].

Karakurt et al., prepared oxime and oxime ether derivatives of anticonvulsant nafimidone [1-(2-naphthyl)-2-(imidozole-1-yl)ethanone] as potential anticonvulsant compounds. Most of the compounds exhibited anticonvulsant activities. Compounds 187, 188 and 189 (salt) were found to be active at 30 mg/kg at the half-hour time point without neurotoxicity at the same dose level (Table 9). Meanwhile, these derivatives exhibited some activity against sc-Met as well as MES-induced seizures [148].

Karakurt et al., reported synthesis of twenty-three new oxime ester derivatives of nafimidone. MES and sc-Met tests were employed for their anticonvulsant activities and rotarod test for neurological deficits. Compound 190 was the most active one in sc-Met test at all dose levels at 4 h (Table 9) [149].

Bansal et al., synthesized O-alkylated derivatives of 1-(2-naphthyl)-2-(imidazol-1-yl)ethanone oxime as potential anticonvulsant compounds. Pre-treatment of mice with compounds 191 and 192 (30 mg/kg, i.p.) significantly decreased the susceptibility to PTZ-induced seizure as evidenced by delayed onset of clonus and mean onset time of extensor phase (Table 8). The treatment of mice with these compounds show equivalent protection level as compared with standard drug diazepam (0.5 mg/kg, i.p.). Anticonvulsant evaluation data showed that compounds 191 and 192 were the most active with ED₅₀ values of 46.77 mg/kg and 24.41 mg/kg, respectively [150].

Karakurt et al., synthesized oxime and oxime ether derivatives of [1-(2-naphthyl)-2-(1,2,4-triazol-1-yl)ethanone] as potential anticonvulsant compounds. The most active of the series was compound 193 (Table 8) [151].

Table 9. Structures of compounds 187–193.

Comp. No.	R	R1	Reference
187		-CH3	[148]
188		-C2H5
189		-CH2CHCH2
190			[149]
191			[150]
192
193		-CH3	[151]

Table 9. Structures of compounds 187–193.

Comp. No.	R	R1	Reference
187		-CH3	[148]
188		-C2H5
189		-CH2CHCH2
190			[149]
191			[150]
192
193		-CH3	[151]

19. The Pyridazine Functional Group

Pyridazine is a heterocyclic organic compound with the molecular formula (CH)₄N₂. It contains a six-membered ring with two adjacent nitrogen atoms, and is aromatic [150]. Pyridazine derivatives have various biological applications [152,153,154,155].

Guan et al., synthesized a series of 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine derivatives. In initial screening and quantitative evaluation, compound 194 was the most active agent, exhibiting the lowest toxicity at the same time (Table 10). In the anti-MES test, it showed ED₅₀ of 17.3 mg/kg and TD₅₀ of 380.3 mg/kg, and the PI of 22.0 which is much better than PI of the reference drugs [156].

Table 10. Structures of compounds 194–200.

Comp. No.	R	R1	R2	Reference
194	-OPh(2,4-Cl2)	H	H	[156]
195	-CH3	H	-CH2Ph	[157]
196	-CH3	H	-CH2Ph(2,6-Cl2)	[158]
197	-CH3	-NH2	-CH2Ph
198	-CH3	-NH2	-CH2Ph(2,6-Cl2)

Table 10. Structures of compounds 194–200.

Comp. No.	R	R1	R2	Reference
194	-OPh(2,4-Cl2)	H	H	[156]
195	-CH3	H	-CH2Ph	[157]
196	-CH3	H	-CH2Ph(2,6-Cl2)	[158]
197	-CH3	-NH2	-CH2Ph
198	-CH3	-NH2	-CH2Ph(2,6-Cl2)

Sivakumar et al., reported synthesis of 1-substituted-1,2-dihydro-pyridazine-3,6-diones as potential anticonvulsant agents. The compounds were tested in vivo for the anticonvulsant activity. The compound which have maximum protection against MES-induced seizures was compound 195 with ED₅₀ = 44.7 mg/kg i.p. 4 h (Table 10) [157].

Moreau et al., reported a synthesis of several 3-substituted pyridazines and a series of imidazo- and triazolopyridazines and tested their anticonvulsant activity against MES-induced seizures in mice. The most active derivatives, 196, 197, 198, 199 and 200 with oral ED₅₀ ranged from 6.2 to 22.0 mg/kg (Table 10). The compound 200 was also protective in the PTZ-induced seizure test (ED₅₀ = 76 mg/kg per os) and blocked strychnine-induced tonic extensor seizures (ED₅₀ = 34.5 mg/kg per os). Furthermore, derivative 200 showed anticonvulsant effects on bicuculline- and yohimbine-induced seizure tests in mice [158].

20. Miscellaneous Functional Groups

Sapa et al., established a synthesis of some novel pyrrolidin-2-one derivatives and evaluated their possible anticonvulsant activity by MES and PTZ tests. Compound 201 significantly reduced the incidence of seizures in the MES test. The compounds 202 and 203 demonstrated activity in the PTZ-induced seizures test [159,160].

Nevagi et al., demonstrated synthesis of novel thiosemicarbazide derivatives and evaluated their anticonvulsant activity and neurotoxicity. Amongst all the synthesized compounds, compound 204 is a broad-spectrum anticonvulsant agent since it was active in both MES- and PTZ-induced seizure models with no neurotoxicity (Figure 12) [161].

Dawidowski et al., synthesized a series of novel diastereomerically pure, monocyclic 2,6-DKP derivatives using a diastereoselective method. In the MES test, some of them showed good or weak antiepileptic activities, however, there was no active compound in the sc-Met screen. The most promising compound 205 exhibited notable action in the 6 Hz test (Figure 12) [162].

Strupińska et al., synthesized a series of benzylamides of isocyclic and heterocyclic acids and tested their anticonvulsant activity. Nearly all synthesized heterocyclic acid derivatives showed anticonvulsant activity. Compound 206 appeared the most promising (Figure 12). It showed in minimal clonic seizure (6 Hz) test (ASP) in rats after i.p. administration: MES ED₅₀ = 36.5 mg/kg, TOX TD₅₀ = 269.75 mg/kg, and PI = 7.39 [163].

Pastore et al., synthesized novel N-derivative-1,2,3-oxathia-zolidine-4-one-2,2-dioxides heterocycles, bioisosteres of trimethadione (TMD, oxazolidine-2,4-dione) and phenytoin. Anticonvulsant screening was performed in mice after intraperitoneal administration in the MES test and sc-PTZ test. Compound 207 (Figure 12), the most active drug obtained, with an ED₅₀ of 60 μg/kg was 10,000 times more active than TMD, the reference compound in this work, and 90 times more active than valproic acid, an anticonvulsant drug presently in use in the clinic [164].

Uysal et al., designed and synthesized sixteen 2/3-benzoylaminopropionanilide derivatives. The anticonvulsant activity profile of the synthesized compounds was determined by MES and sc-Met seizure tests. In the rotarod test, all of them exhibited no toxicity to the nervous system. Compounds 208, 209 and 210 were found to be more potent in the MES or sc-Met tests (Figure 12). Those compounds have emerged as lead compounds for future investigations [165].

Guan et al., prepared a variety of N-(2-hydroxyethyl)cinnamamide derivatives and screened their anticonvulsant activities by the MES test and their neurotoxicity was evaluated by the rotarod test. In the anti-MES potency test, compounds 211 and 212 exhibited ED₅₀ dose of 17.7 and 17.0 mg/kg, respectively (Figure 12), and TD₅₀ dose of 154.9 and 211.1 mg/kg, respectively, resulting in a PI of 8.8 and 12.4, respectively, which were much greater than the PI of the market antiepileptic drug carbamazepine [166].

Alswah et al., reported synthesis of some [1,2,4]triazolo[4,3-a]quinoxaline derivatives as novel anticonvulsant agents. The anticonvulsant evaluation was used metrazol-induced convulsion model and phenobarbitone sodium was as a standard. Among this set of tested compounds, two of them (213 and 214) showed the best anticonvulsant activities (Figure 12) [167].

Chen et al., reported synthesis of 4-(4-alkoxylphenyl)-3-ethyl-4H-1,2,4-triazole derivatives. Their anticonvulsant activities were evaluated by the MES test and their neurotoxicity was evaluated by the rotarod test. MES test showed that compound 215 was found to be the most potent with ED₅₀ value of 8.3 mg/kg and PI value of 5.5, but compound 216 exhibited better PI value of 9.3 (Figure 12), which was much greater than PI value of the prototype drug phenytoin [168].

Figure 12. Structures of compounds 201–227.

Figure 12. Structures of compounds 201–227.

Wang et al., synthesized a series of new purines containing triazole and other heterocycle substituents and evaluated their preliminary anticonvulsant activity and neurotoxicity by using the MES, sc-PTZ and rotarod tests. Among the compounds studied, compound 217 was the most potent compound, with a ED₅₀ of 23.4 mg/kg and a high protective index of more than 25.6 after intraperitoneal administration in mice (Figure 12). Compound 217 showed significant oral activity against MES-induced seizures in mice, with an ED₅₀ of 39.4 mg/kg and a PI above 31.6 [169].

Shu et al., reported synthesis of 4-(3-alkoxy-phenyl)-2,4-dihydro-[1,2,4]triazol-3-ones. All target compounds exhibited anticonvulsant activity of varying degrees in the maximal electroshock test. Compound 218 was the most promising compound with an ED₅₀ value of 30.5 mg/kg and a PI of 18.63 (Figure 12), showing a higher safety than the standard drug carbamazepine (PI = 6.45). In addition, the potency of compound 218 against seizures induced by pentylenetetrazole and 3-mercaptopropionic acid suggested its broad-spectrum activity [170].

Kahveci et al., designed and synthesized a series of new 1,2,4-triazole-3-one derivatives bearing the salicyl moiety. The anticonvulsant activities of all compounds were evaluated by the Anticonvulsant Screening Program of the U.S. National Institutes of Health. The most active compound 219 showed significant anticonvulsant activity with an ED₅₀ of 81.1 mg/kg at an approximate TPE (time of peak effect) of 1 h (Figure 12) [171].

Deng et al., reported a synthesis of 10-alkoxy-5,6-dihydrotriazolo[4,3-d]benzo[f][1,4] oxazepine derivatives and screened their anticonvulsant activities by the MES test and their neurotoxicity was evaluated by the rotarod test. In the MES test, compound 220 was found to possess better anticonvulsant activity and higher safety than market drugs carbamazepine and phenytoin with an ED₅₀ value of 6.9 mg/kg a PI value of 9.5 (Figure 12) [172].

Piao et al., reported a novel series of 9-alkoxy-6,7-dihydro-5H-benzo[c][1,2,4]triazolo[4,3-a] azepine derivatives and screened their anticonvulsant activity by the MES test and the sc-PTZ test. The results revealed that all of the compounds exhibited anticonvulsant activity, compound 221 was found to possess the most potent anticonvulsant activity in the anti-MES potency test (Figure 12), it had a ED₅₀ value of 12.3 mg/kg, a TD₅₀ value of 73.5 mg/kg, and a PI of 6.0, which was slightly lower than the PI of the prototype drug carbamazepine (ED₅₀ = 8.8, PI = 8.1). In the sc-PTZ test, compound 222 was the most active, with an ED₅₀ value of 19.8 mg/kg, a TD₅₀ value of 80.8 mg/kg and a PI value of 4.1, which are greatly higher than that of carbamazepine (ED₅₀ > 100, PI < 0.72) [173].

Deng et al., synthesized two series of 8-alkoxy-4,5-dihydrobenzo[b][1,2,4]triazolo[4,3-d] [1,4]thiazepine derivatives. All of the prepared compounds were effective in the MES screens, among which, compound 223 was considered as the most promising one with an ED₅₀ value of 26.3 mg/kg and a superior PI value of 12.6 (Figure 12). The potency of compound 223 against seizures induced by pentylenetetrazole, 3-mercaptopropionic acid and bicuculline was great too [174].

Ulloora et al., synthesized new substituted 1,4-dihydropyridin-4-yl-phenoxyacetohydrazones. The final compounds were screened for their in vivo anticonvulsant activity by MES, sc-PTZ and 6 Hz methods. The active compounds, 224, 225, 226 and 227 exhibited their activities at 4 h after i.p. injection with 100 mg/kg (Figure 12). All these tested compounds exhibited activity in 6 Hz method within 1 h [175].

Siddiqui et al., reported synthesis of various 1-[6-(4-substituted phenyl)-3-cyano-4-(substituted phenyl)-pyridin-2-yl]-5-oxopyrrolidine-3-carboxylic acids. Their in vivo anticonvulsant evaluation was performed by MES and sc-PTZ tests. Compounds 228 and 229 displayed comparable anticonvulsant activity to the standard drugs with ED₅₀ values of 13.4 and 18.6 mg/kg in electroshock screen, respectively (Figure 13). The compounds 228 and 229 were also found to have encouraging anticonvulsant activity (ED₅₀ = 86.1 and 271.6 mg/kg, respectively) in sc-PTZ screen. Interestingly, they did not show any sign of motor impairment at the maximum dose administered and were not toxic to the liver [176].

Lee et al., prepared 13 derivatives of N-(biphenyl-4′-yl)methyl-(R)-2-acetamido-3-methoxy-propionamide that were tested for anticonvulsant activity at the Anticonvulsant Screening Program (ASP) of the National Institute of Neurological Disorders and Stroke (NINDS) of the U.S. National Institutes of Health. The excellent activities in the MES test (mice, i.p.) of the compound 230 and 231 (ED₅₀ = 9.8 and 12 mg/kg, respectively) coupled with their low neurotoxicities (TD₅₀ = 74 and 86 mg/kg, respectively) provided compounds with notably higher PI (7.6 and 7.2, respectively) (Figure 13) [177].

Siddiqui et al., prepared a series of 4-thiazolidinones bearing a sulfonamide group and tested their anticonvulsant activity utilizing MES and sc-PTZ animal models. Compounds 232, 233 and 234 displayed promising activity and could be considered as leads for further investigations (Figure 13) [178].

Hen et al., synthesized a novel class of 19 carbamates and evaluated their anticonvulsant activity in the rat MES and sc-Met seizure tests and pilocarpine-induced status epilepticus (SE) model. The carbamates 235 (MES ED₅₀ = 64 mg/kg), 236 (MES ED₅₀ = 52 mg/kg) and 237 (MES ED₅₀ = 16 mg/kg) offered an optimal anticonvulsant efficacy and safety profile and consequently are potential candidates for further development as new AEDs (Figure 13) [179].

Hen et al., synthesized a novel class of aromatic amides composed of phenylacetic acid or branched aliphatic carboxylic acids, with five to nine carbons in their carboxylic moiety, and aminobenzenesulfonamide. The final compounds were screened for their anticonvulsant activity by MES and sc-Met tests. The amides 238, 239 and 240 were the most potent compounds possessing MES-ED₅₀ values of 7.6, 9.9, and 9.4 mg/kg and remarkable PI values of 65.7, 50.5, and 53.2, respectively (Figure 13) [180].

Figure 13. Structures of compounds 228–244.

Figure 13. Structures of compounds 228–244.

Guan et al., demonstrated a synthesis of novel series of N-(2-hydroxyethyl)amide derivatives and screened their anticonvulsant activities by the MES test, and their neurotoxicity was evaluated by the rotarod test. The MES test showed that compounds 241, 242 and 243 were found to show a better anticonvulsant activity and also had lower toxicity than the market anti-epileptic drug valproate (Figure 13).

In the anti-MES potency test, these compounds exhibited ED₅₀ doses of 22.0, 23.3, 20.5 mg/kg, respectively, and TD₅₀ doses of 599.8, >1000, >1000 mg/kg, respectively, resulting in a PI of 27.5, >42.9, >48.8, respectively, which are much higher than valproate (PI = 1.6) [181].

Senthilraja et al., synthesized a new series of 2-(4-dimethylaminophenyl)-3-substituted thiazolidin-4-one-5-yl-acetyl acetamides/benzamides. The title compounds were investigated for their anticonvulsant activities, among the test compounds, compound 244 emerged as the most active compound of the series and as moderately more potent than the reference standard diazepam (Figure 13) [182].

21. Conclusions

All in all, based on our laboratory work and the recent literature, this review summarized some significant anticonvulsant compounds which are classified by functional groups and according to data obtained by studies designed in animal models. This review illustrates the various attempts made to discover and develop antiepileptic compounds with more effective and selective effects, and reduced secondary actions. The extensive work reviewed here may represent a starting point to allow a better understanding of antiepileptic therapeutic developments as well as to suggest ideas on design and synthesis of novel antiepileptic compounds.