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Volumn 21, Issue 7, 2012, Pages 1491-1508

New antiepileptic agents: Structure-activity relationships

Author keywords

AED's; Anticonvulsant agents; Structure activity relationships

Indexed keywords

2 PIPERIDINECARBOXYAMIDE DERIVATIVE; 3,3,3 TRIFLUORO 2 HYDROXY 2 PHENYL-PROPIONAMIDE; 5 ADAMANTYLCARBOXAMIDO SULFONAMIDE; 5 PIVALOYLAMIDO1,3,4 THIADIAZOLE 2 SULFONAMIDE; ALKANOLAMIDE; ALPHA(BENZYLAMINO)GAMMA HYDROXYBUTYRIC ACID; ANTICONVULSIVE AGENT; ARYLPIPERAZINE DERIVATIVE; BREVIRACETAM; CARABERSAT; COMPOUND 270664; DENZIMOL; HYDROXYAMIDE DERIVATIVE; INDAZOLE DERIVATIVE; ISATIN DERIVATIVE; LACTAM DERIVATIVE; N (2 CHLOROBENZYLAMIDE); N BENZYLAMIDE; PIPERAZINE; PYRIDAZINONE DERIVATIVE; SULFONAMIDE; THIADIAZOLE DERIVATIVE; THIOSEMICARBAZONE DERIVATIVE; UNCLASSIFIED DRUG; VIGABATRIN; XANTHONE DERIVATIVE;

EID: 84861863732     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-011-9615-3     Document Type: Review
Times cited : (15)

References (136)
  • 2
    • 0033492029 scopus 로고    scopus 로고
    • The anticonvulsant activities of N-benzyl-3-methoxypropionamides
    • Andurkar SV, Stables JP, Kohn H (1999) The anticonvulsant activities of N-benzyl-3-methoxypropionamides. Bioorg Med Chem 7:2381-2389
    • (1999) Bioorg Med Chem , vol.7 , pp. 2381-2389
    • Andurkar, S.V.1    Stables, J.P.2    Kohn, H.3
  • 3
    • 0035953311 scopus 로고    scopus 로고
    • Synthesis and structural studies of aza analogues of functionalized amino acids: New anticonvulsant agents
    • Andurkar SV, Beguin C, Stables JP, Kohn H (2001) Synthesis and structural studies of aza analogues of functionalized amino acids: New anticonvulsant agents. J Med Chem 44:1475-1478
    • (2001) J Med Chem , vol.44 , pp. 1475-1478
    • Andurkar, S.V.1    Beguin, C.2    Stables, J.P.3    Kohn, H.4
  • 4
    • 0034912154 scopus 로고    scopus 로고
    • Competitive AMPA antagonism: A novel mechanism for antiepileptic drugs?
    • Auberson YP (2001) Competitive AMPA antagonism: a novel mechanism for antiepileptic drugs? Drugs Fut 26:463-471
    • (2001) Drugs Fut , vol.26 , pp. 463-471
    • Auberson, Y.P.1
  • 6
    • 0028579819 scopus 로고
    • Synthesis and anticonvulsant activities of α-acetamido-N- benzylacetamide derivatives containing an electron-deficient α-heteroaromatic substituent
    • Bardel P, Bolanos A, Kohn H (1994) Synthesis and anticonvulsant activities of α-acetamido-N-benzylacetamide derivatives containing an electron-deficient α-heteroaromatic substituent. J Med Chem 37:4567-4571
    • (1994) J Med Chem , vol.37 , pp. 4567-4571
    • Bardel, P.1    Bolanos, A.2    Kohn, H.3
  • 9
    • 18244431460 scopus 로고    scopus 로고
    • N-Substituted amino acid N′-benzylamides: Synthesis, anticonvulsant, and metabolic activities
    • Beguin C, LeTiran A, Stables JP, Voyksner RD, Kohn H (2004) N-Substituted amino acid N′-benzylamides: synthesis, anticonvulsant, and metabolic activities. Bioorg Med Chem 12:3079-3096
    • (2004) Bioorg Med Chem , vol.12 , pp. 3079-3096
    • Beguin, C.1    Le Tiran, A.2    Stables, J.P.3    Voyksner, R.D.4    Kohn, H.5
  • 10
    • 0036265090 scopus 로고    scopus 로고
    • The epidemiology of epilepsy: The size of the problem
    • Bell GS, Sander JW (2002) The epidemiology of epilepsy: the size of the problem. Seizure 11(Suppl A):306-314
    • (2002) Seizure , vol.11 , Issue.SUPPL. A , pp. 306-314
    • Bell, G.S.1    Sander, J.W.2
  • 11
    • 0034873696 scopus 로고    scopus 로고
    • Emerging options in the treatment of bipolar disorders
    • Berk M, Segal J, Janet L, Vorster M (2001) Emerging options in the treatment of bipolar disorders. Drugs 61:1407-1414
    • (2001) Drugs , vol.61 , pp. 1407-1414
    • Berk, M.1    Segal, J.2    Janet, L.3    Vorster, M.4
  • 12
    • 0037646298 scopus 로고    scopus 로고
    • 5-HT2C receptor agonists as potential drugs for the treatment of obesity
    • Bickerdike MJ (2003) 5-HT2C receptor agonists as potential drugs for the treatment of obesity. Curr Top Med Chem 3:885-897
    • (2003) Curr Top Med Chem , vol.3 , pp. 885-897
    • Bickerdike, M.J.1
  • 14
    • 0242475190 scopus 로고    scopus 로고
    • New 5-HT2C-receptor agonist expert opinion
    • Bishop MJ, Nilsson BM (2003) New 5-HT2C-receptor agonist expert opinion. Ther Patent 13:1691-1705
    • (2003) Ther. Patent , vol.13 , pp. 1691-1705
    • Bishop, M.J.1    Nilsson, B.M.2
  • 16
    • 0031957398 scopus 로고    scopus 로고
    • Advances in the medical treatment of epilepsy
    • Brazil CW, Pedly TA (1998) Advances in the medical treatment of epilepsy. Ann Rev Med 49:135-162
    • (1998) Ann Rev Med , vol.49 , pp. 135-162
    • Brazil, C.W.1    Pedly, T.A.2
  • 17
    • 0021340965 scopus 로고
    • Synthesis and anticonvulsant activity of some substituted lactams and amides
    • Brouillette WJ, Grunewald GL (1984) Synthesis and anticonvulsant activity of some substituted lactams and amides. J Med Chem 27:202-206
    • (1984) J Med Chem , vol.27 , pp. 202-206
    • Brouillette, W.J.1    Grunewald, G.L.2
  • 19
    • 0033529093 scopus 로고    scopus 로고
    • Comparative molecular field analysis of hydantoin binding to the neuronal voltage-dependent sodium channel
    • Brown MLZCC, Van Dyke CC, Brown GB, Brouillette WJ (1999) Comparative molecular field analysis of hydantoin binding to the neuronal voltage-dependent sodium channel. J Med Chem 42:1537-1545
    • (1999) J Med Chem , vol.42 , pp. 1537-1545
    • Mlzcc, B.1    Van Dyke, C.C.2    Brown, G.B.3    Brouillette, W.J.4
  • 20
    • 0037811293 scopus 로고    scopus 로고
    • Topological virtual screening: A way to find new anticonvulsant drugs from chemical diversity
    • Bruno-Blanch L, Galvez J, Garcia-Domenech R (2003) Topological virtual screening: a way to find new anticonvulsant drugs from chemical diversity. Bioorg Med Chem Lett 13:2749-2754
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 2749-2754
    • Bruno-Blanch, L.1    Galvez, J.2    Garcia-Domenech, R.3
  • 21
    • 0029828946 scopus 로고    scopus 로고
    • Synthesis of novel trans-4-(substituted-benzamido)-3,4-dihydro-2H- benzo[b]pyran-3-ol derivatives as potential anticonvulsant agents with a distinctive binding profile
    • Chan WN, Upton N, Vong AK (1996) Synthesis of novel trans-4-(substituted- benzamido)-3,4-dihydro-2H-benzo[b]pyran-3-ol derivatives as potential anticonvulsant agents with a distinctive binding profile. J Med Chem 39:4537-4539
    • (1996) J Med Chem , vol.39 , pp. 4537-4539
    • Chan, W.N.1    Upton, N.2    Vong, A.K.3
  • 24
    • 0029898015 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activities of N-benzyl-2- acetamidopropionamide derivatives
    • Choi D, Stables JP, Kohn H (1996) Synthesis and anticonvulsant activities of N-benzyl-2-acetamidopropionamide derivatives. J Med Chem 39:1907-1916
    • (1996) J Med Chem , vol.39 , pp. 1907-1916
    • Choi, D.1    Stables, J.P.2    Kohn, H.3
  • 25
    • 0023115854 scopus 로고
    • Functionalized DL-amino acid derivatives. Potent new agents for the treatment of epilepsy
    • Conley JD, Kohn H (1987) Functionalized DL-amino acid derivatives. Potent new agents for the treatment of epilepsy. J Med Chem 30:567-574
    • (1987) J Med Chem , vol.30 , pp. 567-574
    • Conley, J.D.1    Kohn, H.2
  • 26
    • 0003096955 scopus 로고    scopus 로고
    • Recent progress in antiepileptic drug research
    • Robertson DW (ed). Academic Press, San Diego
    • Cosford NDP, McDonald IA, Schweiger EJ (1998) Recent progress in antiepileptic drug research. In: Robertson DW (ed) Annual reports in medicinal chemistry, vol 33. Academic Press, San Diego, pp 61-70
    • (1998) Annual Reports in Medicinal Chemistry , vol.33 , pp. 61-70
    • Cosford, N.D.P.1    McDonald, I.A.2    Schweiger, E.J.3
  • 27
    • 0037606220 scopus 로고    scopus 로고
    • Recent advances in the modulation of voltage-gated ion channels for the treatment of epilepsy
    • Cosford NDP, Meinke PT, Stauderman KA, Hess SD (2002) Recent advances in the modulation of voltage-gated ion channels for the treatment of epilepsy. Curr Drug Targ CNS Neur Dis 1:81-104
    • (2002) Curr Drug Targ CNS Neur Dis , vol.1 , pp. 81-104
    • Cosford, N.D.P.1    Meinke, P.T.2    Stauderman, K.A.3    Hess, S.D.4
  • 28
    • 0024317504 scopus 로고
    • Synthèse et recherche d'une activité anti-convulsivante dans une nouvelle série de diaryl-4,6 pyridazinones-3N-substituées
    • Coudert P, Rubat C, Couquelet J, Fialip J, Bastide P, Privat AM (1989) Synthèse et recherche d'une activité anti-convulsivante dans une nouvelle série de diaryl-4,6 pyridazinones-3N-substituées. Eur J Med Chem 24:551-555
    • (1989) Eur J Med Chem , vol.24 , pp. 551-555
    • Coudert, P.1    Rubat, C.2    Couquelet, J.3    Fialip, J.4    Bastide, P.5    Privat, A.M.6
  • 29
    • 0034762283 scopus 로고    scopus 로고
    • Influence of multidrug resistance (MDR) proteins at the blood-brain barrier on the transport and brain distribution of enaminone anticonvulsants
    • Cox DS, Scott KR, Gao H, Eddington ND (2001) Influence of multidrug resistance (MDR) proteins at the blood-brain barrier on the transport and brain distribution of enaminone anticonvulsants. J Pharm Sci 90:1540-1552
    • (2001) J Pharm Sci , vol.90 , pp. 1540-1552
    • Cox, D.S.1    Scott, K.R.2    Gao, H.3    Eddington, N.D.4
  • 30
    • 0036721587 scopus 로고    scopus 로고
    • Effect of P glycoprotein on the pharmacokinetics and tissue distribution of enaminone anticonvulsants: Analysis by population and physiological approaches
    • Cox DS, Scott KR, Gao H, Eddington ND (2002) Effect of P glycoprotein on the pharmacokinetics and tissue distribution of enaminone anticonvulsants: analysis by population and physiological approaches. J Pharmacol Exp Ther 302:1096-1104
    • (2002) J Pharmacol Exp Ther , vol.302 , pp. 1096-1104
    • Cox, D.S.1    Scott, K.R.2    Gao, H.3    Eddington, N.D.4
  • 31
    • 0035009415 scopus 로고    scopus 로고
    • The new generation of GABA enhancers
    • Czuczwar SJ, Patsalos PN (2001) The new generation of GABA enhancers. CNS Drugs 15:339-350
    • (2001) CNS Drugs , vol.15 , pp. 339-350
    • Czuczwar, S.J.1    Patsalos, P.N.2
  • 32
    • 0029053795 scopus 로고
    • Evaluation of the semicarbazones, thiosemicarbazones and bis-carbohydrazones of some aryl alicyclic ketones for anticonvulsant and other biological properties
    • Dimmock JR, Pandeya SN, Quail JW, Pugazhenthi U, Allen TM, Kao GY, Balzarini J, DeClercq E (1995a) Evaluation of the semicarbazones, thiosemicarbazones and bis-carbohydrazones of some aryl alicyclic ketones for anticonvulsant and other biological properties. Eur J Med Chem 30:303-314
    • (1995) Eur J Med Chem , vol.30 , pp. 303-314
    • Dimmock, J.R.1    Pandeya, S.N.2    Quail, J.W.3    Pugazhenthi, U.4    Allen, T.M.5    Kao, G.Y.6    Balzarini, J.7    Declercq, E.8
  • 34
    • 0029817837 scopus 로고    scopus 로고
    • (Aryloxy) aryl semicarbazones and related compounds: A novel class of anticonvulsant agents possessing high activity in the maximal electroshock screen
    • Dimmock JR, Puthucode RN, Smith JM, Hetherington M, Quail JW, Pugazhenthi U, Lecher T, Stables JP (1996) (Aryloxy) aryl semicarbazones and related compounds: a novel class of anticonvulsant agents possessing high activity in the maximal electroshock screen. J Med Chem 39:3984-3997
    • (1996) J Med Chem , vol.39 , pp. 3984-3997
    • Dimmock, J.R.1    Puthucode, R.N.2    Smith, J.M.3    Hetherington, M.4    Quail, J.W.5    Pugazhenthi, U.6    Lecher, T.7    Stables, J.P.8
  • 35
    • 0034099495 scopus 로고    scopus 로고
    • Anticonvulsant properties of various acetylhydrazones, oxamoylhydrazones and semicarbazones derived from aromatic and unsaturated carbonyl compounds
    • Dimmock JR, Vashishtha SC, Stables JP (2000a) Anticonvulsant properties of various acetylhydrazones, oxamoylhydrazones and semicarbazones derived from aromatic and unsaturated carbonyl compounds. Eur J Med Chem 35:241-248
    • (2000) Eur J Med Chem , vol.35 , pp. 241-248
    • Dimmock, J.R.1    Vashishtha, S.C.2    Stables, J.P.3
  • 37
    • 0036318617 scopus 로고    scopus 로고
    • Synthesis of new 2,5-disubstituted-1,3,4-thiadiazoles and preliminary evaluation of anticonvulsant and antimicrobial activities
    • Dogan HN, Duran A, Rollas S, Sener G, Uysal MK, Gulen D (2002) Synthesis of new 2,5-disubstituted-1,3,4-thiadiazoles and preliminary evaluation of anticonvulsant and antimicrobial activities. Bioorg Med Chem 10:2893-2898
    • (2002) Bioorg Med Chem , vol.10 , pp. 2893-2898
    • Dogan, H.N.1    Duran, A.2    Rollas, S.3    Sener, G.4    Uysal, M.K.5    Gulen, D.6
  • 38
    • 0036202836 scopus 로고    scopus 로고
    • The promise of new antiepileptic drugs
    • Duncan JS (2002) The promise of new antiepileptic drugs. Br J Clin Pharmacol 53:123-131
    • (2002) Br J Clin Pharmacol , vol.53 , pp. 123-131
    • Duncan, J.S.1
  • 39
    • 0035224181 scopus 로고    scopus 로고
    • Can anticonvulsant drug therapy 'cure' epilepsy?
    • Eadie MJ (2001) Can anticonvulsant drug therapy 'cure' epilepsy? CNS Drugs 15:679-690
    • (2001) CNS Drugs , vol.15 , pp. 679-690
    • Eadie, M.J.1
  • 40
    • 0000380375 scopus 로고    scopus 로고
    • Anticonvulsants
    • Wolff E, John ME (eds) therapeutic agents, 5th edn. Wiley, New Jersey
    • Edafiogho I, Scott KR (1996) Anticonvulsants. In: Wolff E, John ME (eds) Burger's medicinal chemistry and drug discovery. Volume 3: therapeutic agents, 5th edn. Wiley, New Jersey, pp 175-260
    • (1996) Burger's Medicinal Chemistry and Drug Discovery , vol.3 , pp. 175-260
    • Edafiogho, I.1    Scott, K.R.2
  • 44
    • 0037367811 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of enaminones. Part 7. Synthesis and anticonvulsant evaluation of ethyl 4-[(substituted phenyl)amino]-6-methyl-2- oxocyclohex-3-ene-1-carboxylates and their corresponding 5-methylcyclohex-2- enone derivatives
    • Eddington ND, Cox DS, Khurana M, Salama NN, Stables JP, Harrison SJ, Negussie A, Taylar RS, Tran UQ, Moore JA, Barrow JC, Scott KR (2003) Synthesis and anticonvulsant activity of enaminones. Part 7. Synthesis and anticonvulsant evaluation of ethyl 4-[(substituted phenyl)amino]-6-methyl-2-oxocyclohex-3-ene- 1-carboxylates and their corresponding 5-methylcyclohex-2-enone derivatives. Eur J Med Chem 38:49-64
    • (2003) Eur J Med Chem , vol.38 , pp. 49-64
    • Eddington, N.D.1    Cox, D.S.2    Khurana, M.3    Salama, N.N.4    Stables, J.P.5    Harrison, S.J.6    Negussie, A.7    Taylar, R.S.8    Tran, U.Q.9    Moore, J.A.10    Barrow, J.C.11    Scott, K.R.12
  • 46
    • 0034091545 scopus 로고    scopus 로고
    • The new antiepileptic drugs: Pharmacological and clinical aspects
    • Gatti G, Bonomi I, Jannuzzi G, Perucca E (2000) The new antiepileptic drugs: pharmacological and clinical aspects. Curr Pharm Des 6:839-860
    • (2000) Curr Pharm des , vol.6 , pp. 839-860
    • Gatti, G.1    Bonomi, I.2    Jannuzzi, G.3    Perucca, E.4
  • 47
    • 70449360465 scopus 로고
    • Structure-activity study of antiepileptic N-aryl-isoxazolecarboxamides/N- isoxazolylbenzamide analogs using Wiener's topological index
    • Goel A, Madan AK (1995) Structure-activity study of antiepileptic N-aryl-isoxazolecarboxamides/N-isoxazolylbenzamide analogs using Wiener's topological index. J Struct Chem 2:155-159
    • (1995) J Struct Chem , vol.2 , pp. 155-159
    • Goel, A.1    Madan, A.K.2
  • 48
    • 0042591180 scopus 로고    scopus 로고
    • Design, synthesis, and development of novel caprolactam anticonvulsants
    • Grimm JB, Stables JP, Brown ML (2003) Design, synthesis, and development of novel caprolactam anticonvulsants. Bioorg Med Chem 11:4133-4141
    • (2003) Bioorg Med Chem , vol.11 , pp. 4133-4141
    • Grimm, J.B.1    Stables, J.P.2    Brown, M.L.3
  • 50
    • 0030608791 scopus 로고    scopus 로고
    • Characterization of the binding of [3H]-SB-204269, a radiolabelled form of the new anticonvulsant SB-204269 (carabersat), to a novel binding site in rat brain membranes
    • Herdon HJ, Jerman JC, Stean TO, Middlemiss DN, Chan WN, Vong AK, Evans JM, Thompson M, Upton N (1997) Characterization of the binding of [3H]-SB-204269, a radiolabelled form of the new anticonvulsant SB-204269 (carabersat), to a novel binding site in rat brain membranes. Brit J Pharmacol 121:1687-1691
    • (1997) Brit J Pharmacol , vol.121 , pp. 1687-1691
    • Herdon, H.J.1    Jerman, J.C.2    Stean, T.O.3    Middlemiss, D.N.4    Chan, W.N.5    Vong, A.K.6    Evans, J.M.7    Thompson, M.8    Upton, N.9
  • 53
    • 0035310335 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of potential anticonvulsants based on 2-piperidinecarboxylic acid and related pharmacophores
    • Ho B, Crider AM, Stables JP (2001) Synthesis and structure-activity relationships of potential anticonvulsants based on 2-piperidinecarboxylic acid and related pharmacophores. Eur J Med Chem 36:265-286
    • (2001) Eur J Med Chem , vol.36 , pp. 265-286
    • Ho, B.1    Crider, A.M.2    Stables, J.P.3
  • 54
    • 2142808112 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors: Aromatic and heterocyclic sulfonamides incorporating adamantyl moieties with strong anticonvulsant activity
    • Ilies MA, Masereel B, Rolin S, Scozzafava A, Campeanu G, Cimpeanu V, Supuran CT (2004) Carbonic anhydrase inhibitors: aromatic and heterocyclic sulfonamides incorporating adamantyl moieties with strong anticonvulsant activity. Bioorg Med Chem 12:271-276
    • (2004) Bioorg Med Chem , vol.12 , pp. 271-276
    • Ma, I.1    Masereel, B.2    Rolin, S.3    Scozzafava, A.4    Campeanu, G.5    Cimpeanu, V.6    Supuran, C.T.7
  • 55
    • 0034957039 scopus 로고    scopus 로고
    • The 5-HT2C receptor as a potential therapeutic target for the design of antiobesity and antiepileptic drugs
    • Isaac M (2001) The 5-HT2C receptor as a potential therapeutic target for the design of antiobesity and antiepileptic drugs. Drugs Fut 26:383-393
    • (2001) Drugs Fut , vol.26 , pp. 383-393
    • Isaac, M.1
  • 56
    • 13444272080 scopus 로고    scopus 로고
    • Serotonergic 5-HT2C receptors as a potential therapeutic target for the design antiepileptic drugs
    • Isaac M (2005) Serotonergic 5-HT2C receptors as a potential therapeutic target for the design antiepileptic drugs. Curr Top Med Chem 5:59-67
    • (2005) Curr Top Med Chem , vol.5 , pp. 59-67
    • Isaac, M.1
  • 57
    • 0041656063 scopus 로고    scopus 로고
    • Antagonists and agonists at the glycine site of the NMDA receptor for therapeutic interventions
    • Jansen M, Dannhardt G (2003) Antagonists and agonists at the glycine site of the NMDA receptor for therapeutic interventions. Eur J Med Chem 38:661-670
    • (2003) Eur J Med Chem , vol.38 , pp. 661-670
    • Jansen, M.1    Dannhardt, G.2
  • 58
    • 0042531889 scopus 로고    scopus 로고
    • Central activity of new xanthone derivatives with chiral center in some pharmacological tests in mice
    • Jastrzebska-Wiesek M, Librowski T, Czarnecki T, Marona H, Nowak G (2003) Central activity of new xanthone derivatives with chiral center in some pharmacological tests in mice. Pol J Pharmacol 55:461-465
    • (2003) Pol J Pharmacol , vol.55 , pp. 461-465
    • Jastrzebska-Wiesek, M.1    Librowski, T.2    Czarnecki, T.3    Marona, H.4    Nowak, G.5
  • 59
    • 0035802403 scopus 로고    scopus 로고
    • Structure and activity studies of glycine receptor ligands. Structural remarks on arylidene-imidazoline-4-one glycinates and glycine amides
    • Karolak-Wojciechowska J, Kiec-Kononowicz K, Mrozek A (2001) Structure and activity studies of glycine receptor ligands. Structural remarks on arylidene-imidazoline-4-one glycinates and glycine amides. J Mol Struct 597:73-81
    • (2001) J Mol Struct , vol.597 , pp. 73-81
    • Karolak-Wojciechowska, J.1    Kiec-Kononowicz, K.2    Mrozek, A.3
  • 60
    • 0037445897 scopus 로고    scopus 로고
    • Structure and activity studies of glycine receptor ligands. Arylidene-imidazoline-4-one amino acids
    • Karolak-Wojciechowska J, Mrozek A, Kiec-Kononowicz K, Handzlik J (2003) Structure and activity studies of glycine receptor ligands. Arylidene- imidazoline-4-one amino acids. J Mol Struct 649:25-36
    • (2003) J Mol Struct , vol.649 , pp. 25-36
    • Karolak-Wojciechowska, J.1    Mrozek, A.2    Kiec-Kononowicz, K.3    Handzlik, J.4
  • 61
    • 0345646399 scopus 로고    scopus 로고
    • Structure and activity studies on glycine receptor ligands. Diphenyl imidazolin-4-one glycine amides
    • Kiec-Kononowicz K, Karolak-Wojciechowska J (1998) Structure and activity studies on glycine receptor ligands. Diphenyl imidazolin-4-one glycine amides. Acta Pol Pharm 55:389-397
    • (1998) Acta Pol Pharm , vol.55 , pp. 389-397
    • Kiec-Kononowicz, K.1    Karolak-Wojciechowska, J.2
  • 62
    • 0038695659 scopus 로고    scopus 로고
    • Glycine derivatives of imidazolones as potential ligands of glycine binding site of NMDA receptors
    • Kiec-Kononowicz K, Karolak-Wojciechowska J, Handzlik J (1998) Glycine derivatives of imidazolones as potential ligands of glycine binding site of NMDA receptors. Acta Pol Pharm 55:381-388
    • (1998) Acta Pol Pharm , vol.55 , pp. 381-388
    • Kiec-Kononowicz, K.1    Karolak-Wojciechowska, J.2    Handzlik, J.3
  • 65
    • 0023690669 scopus 로고
    • Marked stereospecificity in a new class of anticonvulsants
    • Kohn H, Conley JD, Leander JD (1988) Marked stereospecificity in a new class of anticonvulsants. Brain Res 457:371-375
    • (1988) Brain Res , vol.457 , pp. 371-375
    • Kohn, H.1    Conley, J.D.2    Leander, J.D.3
  • 66
    • 0025238774 scopus 로고
    • Preparation and anticonvulsant activity of a series of functionalized α-aromatic and α-heteroaromatic amino acids
    • Kohn H, Sawhney KN, LeGall P, Conley JD, Robertson DW, Leander JD (1990) Preparation and anticonvulsant activity of a series of functionalized α-aromatic and α-heteroaromatic amino acids. J Med Chem 33:919-926
    • (1990) J Med Chem , vol.33 , pp. 919-926
    • Kohn, H.1    Sawhney, K.N.2    Legall, P.3    Conley, J.D.4    Robertson, D.W.5    Leander, J.D.6
  • 67
    • 0026077751 scopus 로고
    • Preparation and anticonvulsant activity of a series of functionalized α-heteroaromatic-substituted amino acids
    • Kohn H, Sawhney KN, LeGall P, Robertson DW, Leander JD (1991) Preparation and anticonvulsant activity of a series of functionalized α- heteroaromatic-substituted amino acids. J Med Chem 34:2444-2452
    • (1991) J Med Chem , vol.34 , pp. 2444-2452
    • Kohn, H.1    Sawhney, K.N.2    Legall, P.3    Robertson, D.W.4    Leander, J.D.5
  • 68
    • 0027443545 scopus 로고
    • Synthesis and anticonvulsant activities of α-heteroaromatic- αacetamido-N-benzylacetamide derivatives
    • Kohn H, Sawhney KH, Bardel P, Robertson DW, Leander JD (1993) Synthesis and anticonvulsant activities of α-heteroaromatic-αacetamido-N- benzylacetamide derivatives. J Med Chem 36: 3350-3360
    • (1993) J Med Chem , vol.36 , pp. 3350-3360
    • Kohn, H.1    Sawhney, K.H.2    Bardel, P.3    Robertson, D.W.4    Leander, J.D.5
  • 69
    • 0028307689 scopus 로고
    • Anticonvulsant properties of N-substituted α, α-diamino acid derivatives
    • Kohn H, Sawhney KN, Robertson DW, Leander JD (1994) Anticonvulsant properties of N-substituted α, α-diamino acid derivatives. J Pharm Sci 83:689-691
    • (1994) J Pharm Sci , vol.83 , pp. 689-691
    • Kohn, H.1    Sawhney, K.N.2    Robertson, D.W.3    Leander, J.D.4
  • 71
    • 0034598762 scopus 로고    scopus 로고
    • Early identification of refractory epilepsies
    • Kwan P, Brodie MJ (2000) Early identification of refractory epilepsies. New Engl J Med 342:314-319
    • (2000) New Engl J Med , vol.342 , pp. 314-319
    • Kwan, P.1    Brodie, M.J.2
  • 72
    • 0034841551 scopus 로고    scopus 로고
    • Functionalized amino acid anticonvulsants: Synthesis and pharmacological evaluation of conformationally restricted analogues
    • Le Tiran A, Stables JP, Kohn H (2001) Functionalized amino acid anticonvulsants: synthesis and pharmacological evaluation of conformationally restricted analogues. Bioorg Med Chem 9:2693-2708
    • (2001) Bioorg Med Chem , vol.9 , pp. 2693-2708
    • Le Tiran, A.1    Stables, J.P.2    Kohn, H.3
  • 73
    • 0037057588 scopus 로고    scopus 로고
    • Design and evaluation of affinity labels of functionalized amino acid anticonvulsants
    • Le Tiran A, Stables JP, Kohn H (2002) Design and evaluation of affinity labels of functionalized amino acid anticonvulsants. J Med Chem 45:4762-4773
    • (2002) J Med Chem , vol.45 , pp. 4762-4773
    • Le Tiran, A.1    Stables, J.P.2    Kohn, H.3
  • 74
    • 0343566431 scopus 로고    scopus 로고
    • The new drugs and strategies to manage epilepsy
    • Lopes Lima JM (2000) The new drugs and strategies to manage epilepsy. Curr Pharm Des 6:873-878
    • (2000) Curr Pharm des , vol.6 , pp. 873-878
    • Lopes Lima, J.M.1
  • 75
    • 0036499726 scopus 로고    scopus 로고
    • Current status and future directions in the pharmacotherapy of epilepsy
    • Loscher WC (2002) Current status and future directions in the pharmacotherapy of epilepsy. Trends Pharmacol Sci 23:113-118
    • (2002) Trends Pharmacol Sci , vol.23 , pp. 113-118
    • Loscher, W.C.1
  • 76
    • 4243308002 scopus 로고    scopus 로고
    • Searching of γ-amino- and γ-hydroxybutyric acid analogues with expected anticonvulsant activity
    • Malawska B (2001) Searching of γ-amino- and γ-hydroxybutyric acid analogues with expected anticonvulsant activity. Wiad Chem 55:377-402
    • (2001) Wiad Chem , vol.55 , pp. 377-402
    • Malawska, B.1
  • 77
    • 0038542930 scopus 로고    scopus 로고
    • Application of pharmacophore models for the design and synthesis of new anticonvulsant drugs
    • Malawska B (2003) Application of pharmacophore models for the design and synthesis of new anticonvulsant drugs. Mini Rev Med Chem 3:341-348
    • (2003) Mini Rev Med Chem , vol.3 , pp. 341-348
    • Malawska, B.1
  • 78
    • 0033055547 scopus 로고    scopus 로고
    • Search for new anticonvulsant compounds, Part 3. Synthesis, physicochemical properties, anticonvulsant activities and voltage-sensitive calcium channels affinity of N-substituted amides of α-(4- phenylpiperazine)-GABA
    • Malawska B, Antkiewicz-Michaluk L (1999) Search for new anticonvulsant compounds, Part 3. Synthesis, physicochemical properties, anticonvulsant activities and voltage-sensitive calcium channels affinity of N-substituted amides of α-(4-phenylpiperazine)-GABA. DiePharmazie 54:239-243
    • (1999) DiePharmazie , vol.54 , pp. 239-243
    • Malawska, B.1    Antkiewicz-Michaluk, L.2
  • 79
    • 0029035245 scopus 로고
    • Synthesis, physicochemical and pharmacological properties of new N-substituted amides of α-piperazine-γ-hydroxybutyric acid
    • Malawska B, Gobaille S (1995) Synthesis, physicochemical and pharmacological properties of new N-substituted amides of α-piperazine- γ-hydroxybutyric acid. DiePharmazie 50:390-393
    • (1995) DiePharmazie , vol.50 , pp. 390-393
    • Malawska, B.1    Gobaille, S.2
  • 80
    • 40949152365 scopus 로고    scopus 로고
    • Brivaracetam: A new drug in development for epilepsy and neuropathic pain
    • Malawska B, Kulig K (2008) Brivaracetam: a new drug in development for epilepsy and neuropathic pain. Exp Opin Investig Drugs 17(3):361-369
    • (2008) Exp Opin Investig Drugs , vol.17 , Issue.3 , pp. 361-369
    • Malawska, B.1    Kulig, K.2
  • 81
    • 0028828388 scopus 로고
    • Search for new anticonvulsant compounds. Part 1: Synthesis, physicochemical and anticonvulsant properties of new derivatives of α-amino-γ-phthalimidobutyric acid
    • Malawska B, Zejc A (1995) Search for new anticonvulsant compounds. Part 1: Synthesis, physicochemical and anticonvulsant properties of new derivatives of α-amino-γ-phthalimidobutyric acid. DiePharmazie 50:722-755
    • (1995) DiePharmazie , vol.50 , pp. 722-755
    • Malawska, B.1    Zejc, A.2
  • 82
    • 0030790189 scopus 로고    scopus 로고
    • Search for new anticonvulsant compounds. Part 2: Structure-activity relationship studies of new N-substituted amides of α-piperazinec- hydroxybutyric acid as active anticonvulsants
    • Malawska B, Kulig K, Ciechanowicz-Rutkowska M (1997) Search for new anticonvulsant compounds. Part 2: Structure-activity relationship studies of new N-substituted amides of α-piperazinec-hydroxybutyric acid as active anticonvulsants. Arch Pharm Pharm Med Chem 330:91-99
    • (1997) Arch Pharm Pharm Med Chem , vol.330 , pp. 91-99
    • Malawska, B.1    Kulig, K.2    Ciechanowicz-Rutkowska, M.3
  • 83
    • 0033052762 scopus 로고    scopus 로고
    • Anticonvulsant activities and voltage-sensitive calcium channels receptor affinity of substituted N-benzylamides of γ-amino- and γ-hydroxybutyric acid
    • Malawska B, Kulig K, Antkiewicz-Michaluk L, Cliffe I, Porter R, Misra A (1999) Anticonvulsant activities and voltage-sensitive calcium channels receptor affinity of substituted N-benzylamides of γ-amino- and γ-hydroxybutyric acid. Arch Pharm Pharm Med Chem 332:167-174
    • (1999) Arch Pharm Pharm Med Chem , vol.332 , pp. 167-174
    • Malawska, B.1    Kulig, K.2    Antkiewicz-Michaluk, L.3    Cliffe, I.4    Porter, R.5    Misra, A.6
  • 84
    • 0344308307 scopus 로고    scopus 로고
    • Comparison of chromatographically determined values of the lipophilicity of anticonvulsant active N-substituted amides of α-arylalkylamine- chydroxybutyric acid with values estimated by computational methods
    • Malawska B, Kulig K, Bendieck E (2003) Comparison of chromatographically determined values of the lipophilicity of anticonvulsant active N-substituted amides of α-arylalkylamine-chydroxybutyric acid with values estimated by computational methods. J Planar Chromatogr 16:390-395
    • (2003) J Planar Chromatogr , vol.16 , pp. 390-395
    • Malawska, B.1    Kulig, K.2    Bendieck, E.3
  • 85
    • 0347761409 scopus 로고    scopus 로고
    • Investigation into new anticonvulsant derivatives of α-subsituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds
    • Malawska B, Kulig K, Spiewak A, Stables JP (2004) Investigation into new anticonvulsant derivatives of α-subsituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds. Bioorg Med Chem 12:625-632
    • (2004) Bioorg Med Chem , vol.12 , pp. 625-632
    • Malawska, B.1    Kulig, K.2    Spiewak, A.3    Stables, J.P.4
  • 86
    • 35048836884 scopus 로고    scopus 로고
    • Design, synthesis and pharmacological evaluation of alpha-substituted N-benzylamides of gamma-hydroxybutyric acid with potential GABAergic activity. Part 6: Search for new anticonvulsant compounds
    • Malawska B, Kulig K, Gajda J, Szczeblewski D, Musial A, Wieckowski K, Maciag D, Stables JP (2007) Design, synthesis and pharmacological evaluation of alpha-substituted N-benzylamides of gamma-hydroxybutyric acid with potential GABAergic activity. Part 6: Search for new anticonvulsant compounds. Acta Pol Pharm 64(2):127-137
    • (2007) Acta Pol Pharm , vol.64 , Issue.2 , pp. 127-137
    • Malawska, B.1    Kulig, K.2    Gajda, J.3    Szczeblewski, D.4    Musial, A.5    Wieckowski, K.6    MacIag, D.7    Stables, J.P.8
  • 87
    • 0031745318 scopus 로고    scopus 로고
    • Evaluation of some 2-substituted derivatives of xanthone for anticonvulsant properties
    • Marona H (1998a) Evaluation of some 2-substituted derivatives of xanthone for anticonvulsant properties. DiePharmazie 53:405-409
    • (1998) DiePharmazie , vol.53 , pp. 405-409
    • Marona, H.1
  • 88
    • 0031668466 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant effects of some aminoalkanolic derivatives of xanthone
    • Marona H (1998b) Synthesis and anticonvulsant effects of some aminoalkanolic derivatives of xanthone. DiePharmazie 53:672-676
    • (1998) DiePharmazie , vol.53 , pp. 672-676
    • Marona, H.1
  • 89
    • 1342290973 scopus 로고    scopus 로고
    • Preliminary evaluation of anticonvulsant activity of some 4-(benzyloxy)-benzamides
    • Marona H, Szneler E (2003) Preliminary evaluation of anticonvulsant activity of some 4-(benzyloxy)-benzamides. Acta Pol Pharm 60: 477-480
    • (2003) Acta Pol Pharm , vol.60 , pp. 477-480
    • Marona, H.1    Szneler, E.2
  • 90
    • 2642611955 scopus 로고    scopus 로고
    • Aminoalkanolic derivatives of xanthone with potential antiepileptic activity
    • Marona H, Gorka Z, Szneler E (1998) Aminoalkanolic derivatives of xanthone with potential antiepileptic activity. DiePharmazie 53:219-223
    • (1998) DiePharmazie , vol.53 , pp. 219-223
    • Marona, H.1    Gorka, Z.2    Szneler, E.3
  • 91
    • 0034938217 scopus 로고    scopus 로고
    • Pharmacological properties of some aminoalkanolic derivatives of xanthone
    • Marona H, Pȩkala E, Filipek B, Macie GD, Szneler E (2001) Pharmacological properties of some aminoalkanolic derivatives of xanthone. DiePharmazie 56:567-572
    • (2001) DiePharmazie , vol.56 , pp. 567-572
    • Marona, H.1    Pȩkala, E.2    Filipek, B.3    MacIe, G.D.4    Szneler, E.5
  • 93
    • 0034189473 scopus 로고    scopus 로고
    • New anti-epileptic drugs for the 21st century
    • McCabe PH (2000) New anti-epileptic drugs for the 21st century. Expert Opin Pharmacother 1:633-674
    • (2000) Expert Opin Pharmacother , vol.1 , pp. 633-674
    • McCabe, P.H.1
  • 94
    • 0033600245 scopus 로고    scopus 로고
    • Emerging Insights into the genesis of epilepsy
    • McNamara JO (1999) Emerging Insights into the genesis of epilepsy. Nature 399:A15-A22
    • (1999) Nature , vol.399
    • McNamara, J.O.1
  • 95
    • 0035695262 scopus 로고    scopus 로고
    • Influence of new γ-aminobutyric acid amide derivatives and its pthalimide precursors on the central nervous system activity in mice
    • Mendyk A, Salat K, Librowski T, Czarnecki T, Malawska B (2001) Influence of new γ-aminobutyric acid amide derivatives and its pthalimide precursors on the central nervous system activity in mice. Pol J Pharmacol 53:689-693
    • (2001) Pol J Pharmacol , vol.53 , pp. 689-693
    • Mendyk, A.1    Salat, K.2    Librowski, T.3    Czarnecki, T.4    Malawska, B.5
  • 96
    • 0035667269 scopus 로고    scopus 로고
    • Future prospects for the drug treatment of epilepsy
    • Nicolson A, Leach JP (2001) Future prospects for the drug treatment of epilepsy. CNS Drugs 15:955-968
    • (2001) CNS Drugs , vol.15 , pp. 955-968
    • Nicolson, A.1    Leach, J.P.2
  • 97
    • 0242551675 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant properties of new N-[(4-arylpiperazin-1-yl)- methyl] derivatives of 3-aryl pyrrolidine-2,5-dione and 2-aza-spiro [4.4] nonane-1,3-dione
    • Obniska J, Zagorska A (2003) Synthesis and anticonvulsant properties of new N-[(4-arylpiperazin-1-yl)-methyl] derivatives of 3-aryl pyrrolidine-2,5- dione and 2-aza-spiro [4.4] nonane-1,3-dione. Farmaco 58:1227-1234
    • (2003) Farmaco , vol.58 , pp. 1227-1234
    • Obniska, J.1    Zagorska, A.2
  • 98
    • 0031947068 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant properties of new N-piperazinylalkyl imides of succinic acid
    • Obniska J, Kulig K, Zejc A (1998) Synthesis and anticonvulsant properties of new N-piperazinylalkyl imides of succinic acid. Acta Pol Pharm 55:223-231
    • (1998) Acta Pol Pharm , vol.55 , pp. 223-231
    • Obniska, J.1    Kulig, K.2    Zejc, A.3
  • 99
    • 0033618470 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant properties of new N-pyridyl derivatives of 3-phenyland 3,3-diphenyl-succinimides
    • Obniska J, Zejc A, Karolak-Wojciechowska J (1999) Synthesis and anticonvulsant properties of new N-pyridyl derivatives of 3-phenyland 3,3-diphenyl-succinimides. Farmaco 54:423-429
    • (1999) Farmaco , vol.54 , pp. 423-429
    • Obniska, J.1    Zejc, A.2    Karolak-Wojciechowska, J.3
  • 100
    • 0036563216 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant properties of new 1-phenyl and 1-phenylamino-3-phenylpyrrolidine-2,5-dione derivatives
    • Obniska J, Zejc A, Zagorska A (2002) Synthesis and anticonvulsant properties of new 1-phenyl and 1-phenylamino-3-phenylpyrrolidine-2,5-dione derivatives. Acta Pol Pharm 59:209-213
    • (2002) Acta Pol Pharm , vol.59 , pp. 209-213
    • Obniska, J.1    Zejc, A.2    Zagorska, A.3
  • 101
    • 0036769051 scopus 로고    scopus 로고
    • Synthesis of isatin semicarbazones as novel anticonvulsants-role of hydrogen
    • Pandeya SN, Raja AS (2002) Synthesis of isatin semicarbazones as novel anticonvulsants-role of hydrogen. J Pharm Sci 5(3): 266-271
    • (2002) J Pharm Sci , vol.5 , Issue.3 , pp. 266-271
    • Pandeya, S.N.1    Raja, A.S.2
  • 102
    • 0032763055 scopus 로고    scopus 로고
    • Evaluation of p-nitrophenyl substituted semicarbazones for anticonvulsant properties
    • Pandeya SN, Ponnilavarasan I, Pandey A, Lakhan R, Stables JP (1999) Evaluation of p-nitrophenyl substituted semicarbazones for anticonvulsant properties. DiePharmazie 54:923-925
    • (1999) DiePharmazie , vol.54 , pp. 923-925
    • Pandeya, S.N.1    Ponnilavarasan, I.2    Pandey, A.3    Lakhan, R.4    Stables, J.P.5
  • 103
    • 0033754195 scopus 로고    scopus 로고
    • Anticonvulsant activity of p-chlorophenyl substituted aryl semicarbazones - The role of primary terminal amino group
    • Pandeya SN, Mishra V, Ponnilavarasan I, Stables JP (2000a) Anticonvulsant activity of p-chlorophenyl substituted aryl semicarbazones - The role of primary terminal amino group. Pol J Pharmacol 52:283-290
    • (2000) Pol J Pharmacol , vol.52 , pp. 283-290
    • Pandeya, S.N.1    Mishra, V.2    Ponnilavarasan, I.3    Stables, J.P.4
  • 104
    • 0033748227 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones
    • Pandeya SN, Yogeeswari P, Stables JP (2000b) Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones. Eur J Med Chem 35:879-886
    • (2000) Eur J Med Chem , vol.35 , pp. 879-886
    • Pandeya, S.N.1    Yogeeswari, P.2    Stables, J.P.3
  • 105
    • 0035109635 scopus 로고    scopus 로고
    • Design of semicarbazones and their bio-isosteric analogues as potential anticonvulsants
    • Pandeya SN, Manjula H, Stables JP (2001a) Design of semicarbazones and their bio-isosteric analogues as potential anticonvulsants. DiePharmazie 56:121-124
    • (2001) DiePharmazie , vol.56 , pp. 121-124
    • Pandeya, S.N.1    Manjula, H.2    Stables, J.P.3
  • 106
    • 0035178865 scopus 로고    scopus 로고
    • Anticonvulsant and neurotoxicity evaluation of 5-(un)-substituted isatinimino derivatives
    • Pandeya SN, Sriram D, Yogeeswari P, Stables JP (2001b) Anticonvulsant and neurotoxicity evaluation of 5-(un)-substituted isatinimino derivatives. DiePharmazie 56:875-876
    • (2001) DiePharmazie , vol.56 , pp. 875-876
    • Pandeya, S.N.1    Sriram, D.2    Yogeeswari, P.3    Stables, J.P.4
  • 107
    • 0037367011 scopus 로고    scopus 로고
    • Design and synthesis of semicarbazones and their bio-isosteric analogues as potent anticonvulsants: The role of hydrogen bonging
    • Pandeya SN, Agarwal AK, Singh A, Stables JP (2003) Design and synthesis of semicarbazones and their bio-isosteric analogues as potent anticonvulsants: the role of hydrogen bonging. Acta Pharm 53:15-24
    • (2003) Acta Pharm , vol.53 , pp. 15-24
    • Pandeya, S.N.1    Agarwal, A.K.2    Singh, A.3    Stables, J.P.4
  • 109
    • 0029936701 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of some amino acid derivatives. Part 2: Derivatives of Gly, Ala, Leu, Pro, Trp, Phe (4Cl), Ala (α-Me)
    • Paruszewski R, Rostafinska-Suchar G, Strupinska M, Jaworski P, Winiecka I, Stables JP (1996b) Synthesis and anticonvulsant activity of some amino acid derivatives. Part 2: Derivatives of Gly, Ala, Leu, Pro, Trp, Phe (4Cl), Ala (α-Me). DiePharmazie 51:212-215
    • (1996) DiePharmazie , vol.51 , pp. 212-215
    • Paruszewski, R.1    Rostafinska-Suchar, G.2    Strupinska, M.3    Jaworski, P.4    Winiecka, I.5    Stables, J.P.6
  • 110
    • 0342514579 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of some amino acid derivatives. Part 3: Derivatives of Ala, Arg, Tzl, Gly and χabu
    • Paruszewski R, Rostafinska-Suchar G, Strupinska M, Winiecka I, Stables JP (2000) Synthesis and anticonvulsant activity of some amino acid derivatives. Part 3: Derivatives of Ala, Arg, Tzl, Gly and χAbu. DiePharmazie 55:27-30
    • (2000) DiePharmazie , vol.55 , pp. 27-30
    • Paruszewski, R.1    Rostafinska-Suchar, G.2    Strupinska, M.3    Winiecka, I.4    Stables, J.P.5
  • 113
    • 84861880471 scopus 로고    scopus 로고
    • The fourth multidisciplinary conferences on drug research Gdańsk-Sobieszewo Book of abstract P-129 Patsalos PN (1999) Ant-epileptic drugs: Newly licensed and under development
    • Paruszewski R, Rostafinska-Suchar G, Strupinska M, Stables JP(2004) The fourth multidisciplinary conferences on drug research, Gdańsk-Sobieszewo, Book of abstract P-129 Patsalos PN (1999) Ant-epileptic drugs: newly licensed and under development. Curr Opin Inv Drugs 1:549-562
    • (2004) Curr Opin Inv Drugs , vol.1 , pp. 549-562
    • Paruszewski, R.1    Rostafinska-Suchar, G.2    Strupinska, M.3    Stables, J.P.4
  • 114
    • 0036150267 scopus 로고    scopus 로고
    • Marketed new antiepileptic drugs: Are they better than old-generation agents?
    • Perucca E (2002) Marketed new antiepileptic drugs: are they better than old-generation agents? Ther Drug Monit 24:74-80
    • (2002) Ther Drug Monit , vol.24 , pp. 74-80
    • Perucca, E.1
  • 115
    • 0021744762 scopus 로고
    • Potential anticonvulsants. IX. Some isatin hydrazones and related compounds
    • Popp FD (1984) Potential anticonvulsants. IX. Some isatin hydrazones and related compounds. J Heteroc Chem 21:1641-1645
    • (1984) J Heteroc Chem , vol.21 , pp. 1641-1645
    • Popp, F.D.1
  • 118
  • 119
    • 0032918385 scopus 로고    scopus 로고
    • Clinical aspects and biological bases of drug-resistant epilepsies
    • Regesta G, Tanganelli P (1999) Clinical aspects and biological bases of drug-resistant epilepsies. Epilepsy Res 34:109-122
    • (1999) Epilepsy Res , vol.34 , pp. 109-122
    • Regesta, G.1    Tanganelli, P.2
  • 120
    • 0025639165 scopus 로고
    • Anticonvulsant activity of 3-oxo-5-substituted benzylidene-6-methyl-(4H)- 2-pyridazinylacetamides and 2-pyridazinylacetylhydrazides
    • Rubat C, Coudert P, Refouvelet B, Tronche P, Bastide P, Bastide P (1990) Anticonvulsant activity of 3-oxo-5-substituted benzylidene-6-methyl-(4H)-2- pyridazinylacetamides and 2-pyridazinylacetylhydrazides. Chem Pharm Bull 38(11):3009-3013
    • (1990) Chem Pharm Bull , vol.38 , Issue.11 , pp. 3009-3013
    • Rubat, C.1    Coudert, P.2    Refouvelet, B.3    Tronche, P.4    Bastide, P.5    Bastide, P.6
  • 121
    • 0036968741 scopus 로고    scopus 로고
    • Influence of new γ-hydroxybutyric acid amide analogues on the central nervous system activity in mice
    • Salat K, Mendyk A, Librowski T, Czarnecki R, Malawska B (2002) Influence of new γ-hydroxybutyric acid amide analogues on the central nervous system activity in mice. Pol J Pharmacol 54:731-736
    • (2002) Pol J Pharmacol , vol.54 , pp. 731-736
    • Salat, K.1    Mendyk, A.2    Librowski, T.3    Czarnecki, R.4    Malawska, B.5
  • 122
    • 0029000782 scopus 로고
    • Development in anticonvulsants
    • Jucker E (ed). Birkhauser Verlag, Basel Boston Berlin
    • Saxena AK, Saxena M (1995) Development in anticonvulsants. In: Jucker E (ed) Progress in drug research, vol 44. Birkhauser Verlag, Basel Boston Berlin, pp 185-291
    • (1995) Progress in Drug Research , vol.44 , pp. 185-291
    • Saxena, A.K.1    Saxena, M.2
  • 124
    • 0037142302 scopus 로고    scopus 로고
    • Quantitative structure-activity relationships analysis of functionalized amino acid anticonvulsant agents using k nearest neighbor and simulated annealing PLS methods
    • Shen M, Le Tiran A, Xiao Y, Golbraikh A, Kohn H, Tropsha A (2002) Quantitative structure-activity relationships analysis of functionalized amino acid anticonvulsant agents using k nearest neighbor and simulated annealing PLS methods. J Med Chem 45:2811-2823
    • (2002) J Med Chem , vol.45 , pp. 2811-2823
    • Shen, M.1    Le Tiran, A.2    Xiao, Y.3    Golbraikh, A.4    Kohn, H.5    Tropsha, A.6
  • 125
    • 3843141802 scopus 로고    scopus 로고
    • Tetramethylcyclopropyl analogue of a leading antiepileptic drug, valproic acid. Synthesis and evaluation of anticonvulsant activity of its amide derivatives
    • Sobol E, Bialer M, Yagen B (2004) Tetramethylcyclopropyl analogue of a leading antiepileptic drug, valproic acid. Synthesis and evaluation of anticonvulsant activity of its amide derivatives. J Med Chem 47(17):4316-4326
    • (2004) J Med Chem , vol.47 , Issue.17 , pp. 4316-4326
    • Sobol, E.1    Bialer, M.2    Yagen, B.3
  • 126
    • 0035997040 scopus 로고    scopus 로고
    • Anticonvulsant activity of hydrazones, Schiff and Mannich bases of isatin derivatives
    • Sridhar SK, Pandeya S, Stables JP, Ramesh A (2002) Anticonvulsant activity of hydrazones, Schiff and Mannich bases of isatin derivatives. Eur J Pharm Sc 16:129-132
    • (2002) Eur J Pharm Sc , vol.16 , pp. 129-132
    • Sridhar, S.K.1    Pandeya, S.2    Stables, J.P.3    Ramesh, A.4
  • 127
    • 1842858323 scopus 로고    scopus 로고
    • Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents
    • Srivastava AVK, Kumar A (2002) Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents. Eur J Med Chem 37:873-882
    • (2002) Eur J Med Chem , vol.37 , pp. 873-882
    • Srivastava, A.V.K.1    Kumar, A.2
  • 128
    • 1342300726 scopus 로고    scopus 로고
    • Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/ thiobarbituric acid as potent anticonvulsant agents
    • Srivastava AVK, Kumar A (2004) Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/thiobarbituric acid as potent anticonvulsant agents. Bioorg Med Chem 12:1257-1264
    • (2004) Bioorg Med Chem , vol.12 , pp. 1257-1264
    • Srivastava, A.V.K.1    Kumar, A.2
  • 129
    • 0031776867 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors. Metal complexes of heterocyclic sulfonamides: A new class of strong topical intraocular pressure-lowering agents with potential use as antiglaucoma drugs
    • Supuran CT, Mincione F, Scozzafava A, Briganti F, Mincione G, Ilies MA (1998) Carbonic anhydrase inhibitors. Metal complexes of heterocyclic sulfonamides: a new class of strong topical intraocular pressure-lowering agents with potential use as antiglaucoma drugs. Eur J Med Chem 33:247-254
    • (1998) Eur J Med Chem , vol.33 , pp. 247-254
    • Supuran, C.T.1    Mincione, F.2    Scozzafava, A.3    Briganti, F.4    Mincione, G.5    Ma, I.6
  • 131
    • 0037413350 scopus 로고    scopus 로고
    • N-, α-, and β-substituted 3aminopropionic acids: Design, syntheses and antiseizure activities
    • Tan CYK, Wainman D, Weaver DF (2003) N-, α-, and β-substituted 3aminopropionic acids: design, syntheses and antiseizure activities. Bioorg Med Chem 11:113-121
    • (2003) Bioorg Med Chem , vol.11 , pp. 113-121
    • Tan, C.Y.K.1    Wainman, D.2    Weaver, D.F.3
  • 133
    • 0036501108 scopus 로고    scopus 로고
    • Anticonvulsant and neurotoxicity evaluation of some 6- chlorobenzothiazolyl-2-thiosemicarbazones
    • Yogeeswari P, Sriram D, Sunil JLR, Kumar SS, Stables JP (2002) Anticonvulsant and neurotoxicity evaluation of some 6-chlorobenzothiazolyl-2- thiosemicarbazones. Eur J Med Chem 37: 231-236
    • (2002) Eur J Med Chem , vol.37 , pp. 231-236
    • Yogeeswari, P.1    Sriram, D.2    Jlr, S.3    Kumar, S.S.4    Stables, J.P.5
  • 135
    • 84861843017 scopus 로고
    • Valproic acid ester with antiepileptic and anticonvulsant activity and pharmaceutical compositions there from
    • Zemp J et al (1984) Valproic acid ester with antiepileptic and anticonvulsant activity and pharmaceutical compositions there from. United States Patent 4442124
    • (1984) United States Patent 4442124
    • Zemp, J.1


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