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Volumn 67, Issue , 2013, Pages 1-13

Design, synthesis and anticonvulsant evaluation of N-(benzo[d]thiazol-2- ylcarbamoyl)-2-methyl-4-oxoquinazoline-3(4H)-carbothioamide derivatives: A hybrid pharmacophore approach

Author keywords

4 Oxoquinazoline 3(4H) carbothioamide; AMPA induced seizure; Anticonvulsant activity; Benzothiazole; Neuroprotection

Indexed keywords

4 AMINOBUTYRIC ACID; ALPHA AMINO 3 HYDROXY 5 METHYL 4 ISOXAZOLEPROPIONIC ACID; ANTICONVULSIVE AGENT; CARBAMAZEPINE; ETHOSUXIMIDE; PHENYTOIN; RILUZOLE;

EID: 84879807393     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.06.026     Document Type: Article
Times cited : (72)

References (51)
  • 1
    • 33746474680 scopus 로고    scopus 로고
    • Epilepsy: A review of selected clinical syndromes and advances in basic science
    • DOI 10.1038/sj.jcbfm.9600265, PII 9600265
    • C.E. Stafstrom, Epilepsy: a review of selected clinical syndromes and advances in basic science, J. Cereb. Blood Flow Metab. 26 (2006) 983-1004. (Pubitemid 44134073)
    • (2006) Journal of Cerebral Blood Flow and Metabolism , vol.26 , Issue.8 , pp. 983-1004
    • Stafstrom, C.E.1
  • 2
  • 3
    • 0345019797 scopus 로고    scopus 로고
    • New visions in the pharmacology of anticonvulsion
    • DOI 10.1016/S0014-2999(97)01514-8, PII S0014299997015148
    • W. Loscher, New visions in the pharmacology of anticonvulsion, Eur. J. Pharmacol. 342 (1998) 1-13. (Pubitemid 28131339)
    • (1998) European Journal of Pharmacology , vol.342 , Issue.1 , pp. 1-13
    • Loscher, W.1
  • 5
    • 0041866161 scopus 로고    scopus 로고
    • Newer anticonvulsants: Dosing strategies and cognition in treating patients with mood disorders and epilepsy
    • K.J.J. Meador, Newer anticonvulsants: dosing strategies and cognition in treating patients with mood disorders and epilepsy, Clin. Psychiatry 64 (2003) 30-34.
    • (2003) Clin. Psychiatry , vol.64 , pp. 30-34
    • Meador, K.J.J.1
  • 6
    • 33845914088 scopus 로고    scopus 로고
    • Novel anticonvulsant drugs
    • DOI 10.1016/j.pharmthera.2006.07.005, PII S0163725806001379
    • H. Stefan, T. Feuerstein, Novel anticonvulsant drugs, Pharmacol. Ther. 113 (2007) 165-183. (Pubitemid 46017070)
    • (2007) Pharmacology and Therapeutics , vol.113 , Issue.1 , pp. 165-183
    • Stefan, H.1    Feuerstein, T.J.2
  • 7
    • 33646144219 scopus 로고    scopus 로고
    • New Generation Anticonvulsants for the Treatment of Epilepsy in Children
    • DOI 10.1016/j.nurx.2006.01.013, PII S1545534306000320
    • E.J. Donner, O.C. Snead III, New generation anticonvulsants for the treatment of epilepsy in children, NeuroRX 3 (2006) 170-180. (Pubitemid 44081770)
    • (2006) NeuroRx , vol.3 , Issue.2 , pp. 170-180
    • Donner, E.J.1    Snead III, O.C.2
  • 8
    • 4644301804 scopus 로고    scopus 로고
    • Progress report on new antiepileptic drugs: A summary of the Seventh Eilat Conference (EILAT VII)
    • DOI 10.1016/j.eplepsyres.2004.07.010, PII S0920121104001457
    • M. Bialer, S.I. Johannessen, H.J. Kupferberg, R.H. Levy, E. Perucca, T. Tomson, Progress report on new antiepileptic drugs: a summary of the Seventh Eilat Conference (EILAT VII), Epilepsy Res. 61 (2004) 1-48. (Pubitemid 39296697)
    • (2004) Epilepsy Research , vol.61 , Issue.1-3 , pp. 1-48
    • Bialer, M.1    Johannessen, S.I.2    Kupferberg, H.J.3    Levy, R.H.4    Perucca, E.5    Tomson, T.6
  • 9
    • 1842858323 scopus 로고    scopus 로고
    • Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents
    • DOI 10.1016/S0223-5234(02)01389-2, PII S0223523402013892
    • A.V.K. Srivastava, A. Kumar, Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents, Eur. J. Med. Chem. 37 (2002) 873-882. (Pubitemid 35356423)
    • (2002) European Journal of Medicinal Chemistry , vol.37 , Issue.11 , pp. 873-882
    • Archana1    Srivastava, V.K.2    Kumar, A.3
  • 10
    • 1342300726 scopus 로고    scopus 로고
    • Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/ thiobarbituric acid as potent anticonvulsant agents
    • DOI 10.1016/j.bmc.2003.08.035
    • A.V.K. Srivastava, A. Kumar, Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/thiobarbituric acid as potent anticonvulsant agents, Bioorg. Med. Chem. 12 (2004) 1257-1264. (Pubitemid 38251316)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.5 , pp. 1257-1264
    • Archana1    Srivastava, V.K.2    Kumar, A.3
  • 11
    • 0025796651 scopus 로고
    • Synthesis and evaluation of some CNS depressant properties of 3-{2-[(5-aryl-1,3,4-oxadiazol-2yl)amino] acetamido}-2-methyl-4(3H)- quinazolinones
    • N. Ergenc, S. Buyuktimkin, G. Capan, G. Baktir, S. Rollas, Synthesis and evaluation of some CNS depressant properties of 3-{2-[(5-aryl-1,3,4-oxadiazol- 2yl)amino] acetamido}-2-methyl-4(3H)-quinazolinones, Pharmazie 46 (1991) 290-291.
    • (1991) Pharmazie , vol.46 , pp. 290-291
    • Ergenc, N.1    Buyuktimkin, S.2    Capan, G.3    Baktir, G.4    Rollas, S.5
  • 12
    • 51449122251 scopus 로고    scopus 로고
    • Design, synthesis and potential CNS activity of some novel 1-(4-substituted-phenyl)-3-(4-oxo-2-propyl-4H-quinazolin-3-yl)-urea
    • S.K. Kashaw, V. Kashaw, P. Mishra, N.K. Jain, Design, synthesis and potential CNS activity of some novel 1-(4-substituted-phenyl)-3-(4-oxo-2-propyl- 4H-quinazolin-3-yl)-urea, ARKIVOC xiv (2008) 17-26.
    • (2008) ARKIVOC , vol.14 , pp. 17-26
    • Kashaw, S.K.1    Kashaw, V.2    Mishra, P.3    Jain, N.K.4
  • 13
    • 84875917035 scopus 로고    scopus 로고
    • Synthesis, anticonvulsant, antioxidant and binding interaction of novel N-substituted methyl quinazoline-2,4(1H,3H)-dione derivatives to bovine serum albumin: A structure-activity relationship study, Spectrochim
    • M.K. Prashantha, M. Madaiaha, H.D. Revanasiddappaa, B. Veereshb, Synthesis, anticonvulsant, antioxidant and binding interaction of novel N-substituted methyl quinazoline-2,4(1H,3H)-dione derivatives to bovine serum albumin: a structure-activity relationship study, Spectrochim. Acta Part A: Mol. Biomol. Spectrosc. 110 (2013) 324-332.
    • (2013) Acta Part A: Mol. Biomol. Spectrosc. , vol.110 , pp. 324-332
    • Prashantha, M.K.1    Madaiaha, M.2    Revanasiddappaa, H.D.3    Veereshb, B.4
  • 14
    • 84857356050 scopus 로고    scopus 로고
    • Design and synthesis of novel 7-aminoquinazoline derivatives: Antitumor and anticonvulsant activities
    • A.S. El-Azab, K.E.H. ElTahir, Design and synthesis of novel 7-aminoquinazoline derivatives: antitumor and anticonvulsant activities, Bioorg. Med. Chem. 22 (2012) 1879-1885.
    • (2012) Bioorg. Med. Chem. , vol.22 , pp. 1879-1885
    • El-Azab, A.S.1    ElTahir, K.E.H.2
  • 17
    • 0016784677 scopus 로고
    • Synthesis of 2-(4-arylthiosemicarbazidocarbonylthio)benzothiazoles and their monamine oxidase inhibitory and anticonvulsant properties
    • S.P. Singh, R.S. Misra, S.S. Parmar, S.J. Brumleve, Synthesis of 2-(4-arylthiosemicarbazidocarbonylthio)benzothiazoles and their monamine oxidase inhibitory and anticonvulsant properties, J. Pharm. Sci. 64 (1975) 1245-1247.
    • (1975) J. Pharm. Sci. , vol.64 , pp. 1245-1247
    • Singh, S.P.1    Misra, R.S.2    Parmar, S.S.3    Brumleve, S.J.4
  • 18
    • 77955440451 scopus 로고    scopus 로고
    • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) antagonists: From bench to bedside
    • H. Mattes, D. Carcache, H.O. Kalkman, M. Koller, alpha-Amino-3-hydroxy-5- methyl-4-isoxazolepropionic acid (AMPA) antagonists: from bench to bedside, J. Med. Chem. 53 (2010) 5367-5382.
    • (2010) J. Med. Chem. , vol.53 , pp. 5367-5382
    • Mattes, H.1    Carcache, D.2    Kalkman, H.O.3    Koller, M.4
  • 19
    • 0035179658 scopus 로고    scopus 로고
    • NMDA Receptor regulation of memory and behavior in humans
    • DOI 10.1002/hipo.1069
    • J.W. Newcomer, J.H. Krystal, NMDA receptor regulation of memory and behavior in humans, Hippocampus 11 (2001) 529-542. (Pubitemid 33100374)
    • (2001) Hippocampus , vol.11 , Issue.5 , pp. 529-542
    • Newcomer, J.W.1    Krystal, J.H.2
  • 20
    • 80051794718 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant evaluation of some novel 4(3H)-quinazolinones
    • A.S. El-Azab, K.E.H. ElTahir, M.S. Attia, Synthesis and anticonvulsant evaluation of some novel 4(3H)-quinazolinones, Monatsh. Chem. 142 (2011) 837-848.
    • (2011) Monatsh. Chem. , vol.142 , pp. 837-848
    • El-Azab, A.S.1    ElTahir, K.E.H.2    Attia, M.S.3
  • 21
    • 0039736616 scopus 로고
    • Evaluation of anticonvulsant activity of 2,3 di-substituted quinazolones: A new class of anticonvulsant drugs
    • M.L. Gujral, K.N. Sareen, R.P.E. Kohli, Evaluation of anticonvulsant activity of 2,3 di-substituted quinazolones: a new class of anticonvulsant drugs, Ind. J. Med. Res. 45 (1957) 207-210.
    • (1957) Ind. J. Med. Res. , vol.45 , pp. 207-210
    • Gujral, M.L.1    Sareen, K.N.2    Kohli, R.P.E.3
  • 22
    • 79961078010 scopus 로고
    • Potential anticonvulsants: Synthesis of 2,3-substituted 4-quinazolones & quinazolo-4-thiones
    • A.P. Bhaduri, N.M. Khanna, M.L. Dhar, Potential anticonvulsants: synthesis of 2,3-substituted 4-quinazolones & quinazolo-4-thiones, Ind. J. Chem. 2 (1964) 159-161.
    • (1964) Ind. J. Chem. , vol.2 , pp. 159-161
    • Bhaduri, A.P.1    Khanna, N.M.2    Dhar, M.L.3
  • 23
    • 84655164783 scopus 로고
    • Synthesis of 6-halogenated. 2,3-Disubstituted-4-quinazolinones III
    • S.R. Salimath, N.M.J. Patelshah, Synthesis of 6-halogenated. 2,3-Disubstituted-4-quinazolinones III, Ind. Chem. Soc. 33 (1956) 140-146.
    • (1956) Ind. Chem. Soc. , vol.33 , pp. 140-146
    • Salimath, S.R.1    Patelshah, N.M.J.2
  • 24
    • 84655175048 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant evaluation of some new2, 3,8-trisubstituted-4(3H)-quinazoline derivatives
    • A.S. El-Azab, K.E.H. ElTahir, Synthesis and anticonvulsant evaluation of some new2, 3,8-trisubstituted-4(3H)-quinazoline derivatives, Bioorg. Med. Chem. Lett. 22 (2012) 327-333.
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 327-333
    • El-Azab, A.S.1    ElTahir, K.E.H.2
  • 25
    • 0019459495 scopus 로고
    • GABA-benzodiazepine-barbiturate receptor interaction
    • R.W.J. Olsen, GABA-benzodiazepine-barbiturate receptor interaction, J. Neurochem. 27 (1981) 1-3.
    • (1981) J. Neurochem. , vol.27 , pp. 1-3
    • Olsen, R.W.J.1
  • 26
    • 0023757524 scopus 로고
    • Pentylenetetrazole inhibits glutamate dehydrogenase and aspartate aminotransferase, and stimulates GABA aminotransferase in homogenates from rat cerebral cortex
    • L. Lacoste, S. Bartolucci, J.C. Lapointe, Pentylenetetrazole inhibits glutamate dehydrogenase and aspartate aminotransferase, and stimulates GABA amino transferase in homogenates from rat cerebral cortex, Can. J. Physiol. Pharmacol. 66 (1988) 1135-1138. (Pubitemid 18259797)
    • (1988) Canadian Journal of Physiology and Pharmacology , vol.66 , Issue.9 , pp. 1135-1138
    • Lacoste, L.1    Bartolucci, S.2    Lapointe, J.3
  • 27
    • 0024494416 scopus 로고
    • The role of the nigrotegmental GABAergic pathway in the propagation of pentylenetetrazol-induced seizures
    • DOI 10.1016/0006-8993(89)90212-6
    • R. Okada, H. Negishi, The role of the nigrotegmental GABAergic pathway in the propagation of pentylenetetrazole-induced seizures, Brain Res. 480 (1989) 383-387. (Pubitemid 19050241)
    • (1989) Brain Research , vol.480 , Issue.1-2 , pp. 383-387
    • Okada, R.1    Negishi, N.2    Nagaya, H.3
  • 28
    • 0033748227 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones
    • S.N. Pandeya, P. Yogeeswari, J.P. Stables, Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones, Eur. J. Med. Chem. 35 (2000) 879-886.
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 879-886
    • Pandeya, S.N.1    Yogeeswari, P.2    Stables, J.P.3
  • 29
    • 0036501108 scopus 로고    scopus 로고
    • Anticonvulsant and neurotoxicity evaluation of some 6- chlorobenzothiazolyl-2-thiosemicarbazones
    • DOI 10.1016/S0223-5234(02)01338-7, PII S0223523402013387
    • P. Yogeeswari, D. Sriram, L.R.J. Suniljit, S.S. Kumar, J.P. Stables, Anticonvulsant and neurotoxicity evaluation of some 6-chlorobenzothiazolyl-2- thiosemicarbazones, Eur. J. Med. Chem. 37 (2002) 231-236. (Pubitemid 34251186)
    • (2002) European Journal of Medicinal Chemistry , vol.37 , Issue.3 , pp. 231-236
    • Yogeeswari, P.1    Sriram, D.2    Sunil, J.L.R.J.3    Kumar, S.S.4    Stables, J.P.5
  • 30
    • 79952701822 scopus 로고    scopus 로고
    • Synthesis, anticonvulsant and toxicity screening of thiazolyl-thiadiazole derivatives
    • N. Siddiqui, W. Ahsan, Synthesis, anticonvulsant and toxicity screening of thiazolyl-thiadiazole derivatives, Med. Chem. Res. 20 (2011) 216-226.
    • (2011) Med. Chem. Res. , vol.20 , pp. 216-226
    • Siddiqui, N.1    Ahsan, W.2
  • 31
    • 77949442787 scopus 로고    scopus 로고
    • Synthesis and preliminary screening of benzothiazol-2-yl thiadiazole derivatives for anticonvulsant activity
    • N. Siddiqui, A. Rana, S.A. Khan, S.E. Haque, M.F. Arshad, S. Ahmed, W. Ahsan, Synthesis and preliminary screening of benzothiazol-2-yl thiadiazole derivatives for anticonvulsant activity, Acta Pharm. 59 (2009) 441-451.
    • (2009) Acta Pharm. , vol.59 , pp. 441-451
    • Siddiqui, N.1    Rana, A.2    Khan, S.A.3    Haque, S.E.4    Arshad, M.F.5    Ahmed, S.6    Ahsan, W.7
  • 32
    • 33947436462 scopus 로고
    • A new synthesis of 4-quinazolones
    • H.W. Grimmel, A. Guentin, A new synthesis of 4-quinazolones, J. Am. Chem. Soc. 68 (1946) 542-543.
    • (1946) J. Am. Chem. Soc. , vol.68 , pp. 542-543
    • Grimmel, H.W.1    Guentin, A.2
  • 33
    • 0033556619 scopus 로고    scopus 로고
    • Synthesis of 2-heterosubstituted quinazolinone atropisomeric phosphine ligands by direct lithiation of a 2-unsubstituted quinazolinone system
    • DOI 10.1016/S0957-4166(98)00496-0, PII S0957416698004960
    • X. Dai, S. Virgil, Synthesis of 2-heterosubstituted quinazolinone atropisomeric phosphine ligands by direct lithiation of a 2-unsubstituted quinazolinone system, Tetrahedron: Asymmetry 10 (1999) 25-29. (Pubitemid 29089204)
    • (1999) Tetrahedron Asymmetry , vol.10 , Issue.1 , pp. 25-29
    • Dai, X.1    Virgil, S.2
  • 34
    • 57949102174 scopus 로고    scopus 로고
    • Synthesis of some novel N4-(naphtha[1,2-d]thiazol-2-yl)semicarbazides as potential anticonvulsants
    • F. Azam, I.A. Alkskas, S.L. Khora, O. Prakash, Synthesis of some novel N4-(naphtha[1,2-d]thiazol-2-yl)semicarbazides as potential anticonvulsants, Eur. J. Med. Chem. 44 (2009) 203-211.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 203-211
    • Azam, F.1    Alkskas, I.A.2    Khora, S.L.3    Prakash, O.4
  • 36
    • 0021611548 scopus 로고
    • Antiepileptic drug development program
    • R.J. Porter, J.J. Cereghino, G.D. Gladding, B.J. Hessie, H.J. Kupferberg, B. Scoville, B.G. White, Antiepileptic drug development program, Cleve. Clin. Q. 51 (1984) 293-305. (Pubitemid 14038030)
    • (1984) Cleveland Clinic Quarterly , vol.51 , Issue.2 , pp. 293-305
    • Porter, R.J.1    Cereghino, J.J.2    Gladding, G.D.3
  • 38
    • 84951384024 scopus 로고
    • A simplified method of evaluating dose-effect experiments
    • J.T. Litchfield, F.A. Wilcoxon, A simplified method of evaluating dose-effect experiments, J. Pharmacol. Exp. Ther. 96 (1949) 99-113.
    • (1949) J. Pharmacol. Exp. Ther. , vol.96 , pp. 99-113
    • Litchfield, J.T.1    Wilcoxon, F.A.2
  • 40
    • 70449177837 scopus 로고
    • A note on a simple apparatus for detecting neurological deficit in rats and mice
    • N.W. Dunham, T.A. Miya, A note on a simple apparatus for detecting neurological deficit in rats and mice, J. Am. Pharm. Assoc. Sci. 46 (1957) 208-209.
    • (1957) J. Am. Pharm. Assoc. Sci. , vol.46 , pp. 208-209
    • Dunham, N.W.1    Miya, T.A.2
  • 41
    • 0000397013 scopus 로고
    • Comparative assay of antiepileptic drugs by psychomotor seizure test and minimal electroshock threshold test
    • W.C. Brown, D.O. Schiffman, E.A. Swinyard, L.S. Goodman, Comparative assay of antiepileptic drugs by psychomotor seizure test and minimal electroshock threshold test, J. Pharmacol. Exp. Ther. 107 (1953) 273-283.
    • (1953) J. Pharmacol. Exp. Ther. , vol.107 , pp. 273-283
    • Brown, W.C.1    Schiffman, D.O.2    Swinyard, E.A.3    Goodman, L.S.4
  • 42
    • 0035652290 scopus 로고    scopus 로고
    • Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy
    • DOI 10.1016/S0920-1211(01)00302-3, PII S0920121101003023
    • M.E. Barton, B.D. Klein, H.H. Wolf, H.S. White, Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy, Epilepsy Res. 47 (2001) 217-227. (Pubitemid 34008465)
    • (2001) Epilepsy Research , vol.47 , Issue.3 , pp. 217-227
    • Barton, M.E.1    Klein, B.D.2    Wolf, H.H.3    White, H.S.4
  • 43
    • 3042816099 scopus 로고    scopus 로고
    • A receptors protect against partial seizures induced by 6-Hz electrical stimulation in mice
    • DOI 10.1111/j.0013-9580.2004.04504.x
    • R.F. Kaminski, M.R. Livingood, M.A. Rogawski, Allopregnanolone analogs that positively modulate GABA receptors protect against partial seizures induced by 6-Hz electrical stimulation in mice, Epilepsia 45 (2004) 864-867. (Pubitemid 38890989)
    • (2004) Epilepsia , vol.45 , Issue.7 , pp. 864-867
    • Kaminski, R.M.1    Livingood, M.R.2    Rogawski, M.A.3
  • 44
    • 33644982586 scopus 로고    scopus 로고
    • 2,4-Dimethoxyphenyl semicarbazones with anticonvulsant activity against three animal models of seizure: Synthesis and pharmacological evaluation
    • R. Thirumurugan, D. Sriram, A. Saxena, J.P. Stables, P. Yogeeswari, 2,4-Dimethoxyphenyl semicarbazones with anticonvulsant activity against three animal models of seizure: synthesis and pharmacological evaluation, Bioorg. Med. Chem. 14 (2006) 3106-3112.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 3106-3112
    • Thirumurugan, R.1    Sriram, D.2    Saxena, A.3    Stables, J.P.4    Yogeeswari, P.5
  • 45
    • 0344389594 scopus 로고
    • Evidence for increased serum glutamic oxalacetic transaminase (SGO-T) activity following graded myocardial infarcts in dogs
    • I. Nydick, F. Wrobelewski, J.S. Ladue, Evidence for increased serum glutamic oxalacetic transaminase (SGO-T) activity following graded myocardial infarcts in dogs, Circulation 22 (1955) 161-163.
    • (1955) Circulation , vol.22 , pp. 161-163
    • Nydick, I.1    Wrobelewski, F.2    Ladue, J.S.3
  • 46
    • 66349129125 scopus 로고
    • A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases
    • S. Reitman, S. Frankel, A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases, Am. J. Clin. Pathol. 28 (1957) 56-58.
    • (1957) Am. J. Clin. Pathol. , vol.28 , pp. 56-58
    • Reitman, S.1    Frankel, S.2
  • 47
    • 0347880244 scopus 로고
    • Academic Press, New York
    • E. Roberts, Methods in Enzymology, vol. VI, Academic Press, New York, 1962, p. 612.
    • (1962) Methods in Enzymology , vol.6 , pp. 612
    • Roberts, E.1
  • 48
    • 0028021395 scopus 로고
    • Excitatory amino acid neurotransmission through both NMDA and non-NMDA receptors is involved in the anticonvulsant activity of felbamate in DBA/2 mice
    • G.B. De Sarro, E. Ongini, R. Bertorelli, U. Aguglia, A. De Sarro, Excitatory amino acid neurotransmission through both NMDA and non-NMDA receptors is involved in the anticonvulsant activity of felbamate in DBA:2 mice, Eur. J. Pharmacol. 262 (1994) 11-19. (Pubitemid 24271831)
    • (1994) European Journal of Pharmacology , vol.262 , Issue.1-2 , pp. 11-19
    • De Sarro, G.1    Ongini, E.2    Bertorelli, R.3    Aguglia, U.4    De Sarro, A.5
  • 49
    • 0027404879 scopus 로고
    • GYKI 52466, a 2,3-benzodiazepine, is a highly selective, noncompetitive antagonist of AMPA/kainate receptor responses
    • DOI 10.1016/0896-6273(93)90241-I
    • S.D. Donevan, M.A. Rogawski, GYKI 52466, a 2,3-benzodiazepine, is a highly selective, non-competitive antagonist of AMPA: kainate receptor responses, Neuron 10 (1993) 51-59. (Pubitemid 23045425)
    • (1993) Neuron , vol.10 , Issue.1 , pp. 51-59
    • Donevan, S.D.1    Rogawski, M.A.2
  • 50
    • 0027176541 scopus 로고
    • Therapeutic potential of excitatory amino acid antagonists: Channel blockers and 2,3-benzodiazepines
    • M.A. Rogawski, Therapeutic potential of excitatory amino acid antagonists: channel blockers and 2,3-benzodiazepines, Trends Pharmacol. Sci. 14 (1993) 325-331. (Pubitemid 23282161)
    • (1993) Trends in Pharmacological Sciences , vol.14 , Issue.9 , pp. 325-331
    • Rogawski, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.