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With respect to our first finding of the derivatives, see: Sakamoto, S.; Ohmori, J.; Shimizu-Sasamata, M.; Okada, M.; Hidaka, K. Pat. Appl. WO 93/20077, 1993. On the other hand, another series of heterocyclic-fused quinoxalinones were found as glycine and glycine/AMPA antagonists by Ely Lilly (McQuaid, L. A.; Mitch, C. H.; Ornstein, P. L.; Schoepp, M. D. D.; Smith, E. C. R. Pat. Appl. US 5196421, 1993), ICI (Jackson, P. F.; Davenport, T. W.; Resch, J. F.; Lehr, G. S.; Pullan, L. M. Tricyclic Quinoxalines as Ligands for the Strychnine-insensitive Glycine Site. Bioorg. Med. Chem. Lett. 1991, 1, 751-756), and Novo Nordisk (Jacobsen, P.; Nielsen, F. E. Pat. Appl. WO 93/06103, 1993) independently around the same time.
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With respect to our first finding of the derivatives, see: Sakamoto, S.; Ohmori, J.; Shimizu-Sasamata, M.; Okada, M.; Hidaka, K. Pat. Appl. WO 93/20077, 1993. On the other hand, another series of heterocyclic-fused quinoxalinones were found as glycine and glycine/AMPA antagonists by Ely Lilly (McQuaid, L. A.; Mitch, C. H.; Ornstein, P. L.; Schoepp, M. D. D.; Smith, E. C. R. Pat. Appl. US 5196421, 1993), ICI (Jackson, P. F.; Davenport, T. W.; Resch, J. F.; Lehr, G. S.; Pullan, L. M. Tricyclic Quinoxalines as Ligands for the Strychnine-insensitive Glycine Site. Bioorg. Med. Chem. Lett. 1991, 1, 751-756), and Novo Nordisk (Jacobsen, P.; Nielsen, F. E. Pat. Appl. WO 93/06103, 1993) independently around the same time.
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Ohmori, J.; Shimizu-Sasamata, M.; Okada, M.; Kawasaki, S.; Togami, J.; Murase, K.; Sakamoto, S. Synthesis and Structure-Activity Relationships of Excitatory Amino Acid Receptor (AMPA subtype) Antagonist 2. Presented at the 113th Meeting of the Pharmaceutical Society of Japan, March 1993; Abstract 29PB10-07.
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(1993)
113th Meeting of the Pharmaceutical Society of Japan
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Ohmori, J.1
Shimizu-Sasamata, M.2
Okada, M.3
Kawasaki, S.4
Togami, J.5
Murase, K.6
Sakamoto, S.7
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34
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0026746060
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Synthesis and Excitatory Amino Acid Pharmacology of a Series of Heterocyclic-Fused Quinoxalinones and Quinazolinones
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McQuaid, L. A.; Smith, E. C. R.; South, K. K.; Mitch, C. H.; Schoepp, M. D. D.; True, B. A.; Calligaro, D. O.; O'Malley, P. J.; Lodge, D.; Ornstein, P. L. Synthesis and Excitatory Amino Acid Pharmacology of a Series of Heterocyclic-Fused Quinoxalinones and Quinazolinones. J. Med. Chem. 1992, 35, 3319-3324.
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J. Med. Chem.
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McQuaid, L.A.1
Smith, E.C.R.2
South, K.K.3
Mitch, C.H.4
Schoepp, M.D.D.5
True, B.A.6
Calligaro, D.O.7
O'Malley, P.J.8
Lodge, D.9
Ornstein, P.L.10
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35
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0027331481
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3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory Amino Acid Antagonists Acting at Glycine-Site NMDA and (RS)-α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors
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Carting, W. R.; Leeson, P. D.; Moore, K. W.; Smith, J. D.; Moyes, C. R.; Mawer, I. M.; Thomas, S.; Chan, T.; Baker, R.; Foster, A. C.; Grimwood, S.; Kemp, J. A.; Marshall, G. R.; Tricklebank, M. D.; Saywell, K. L. 3-Nitro-3,4-dihydro-2(1H)-quinolones. Excitatory Amino Acid Antagonists Acting at Glycine-Site NMDA and (RS)-α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid Receptors. J. Med. Chem. 1993, 36, 3397-3408.
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J. Med. Chem.
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Carting, W.R.1
Leeson, P.D.2
Moore, K.W.3
Smith, J.D.4
Moyes, C.R.5
Mawer, I.M.6
Thomas, S.7
Chan, T.8
Baker, R.9
Foster, A.C.10
Grimwood, S.11
Kemp, J.A.12
Marshall, G.R.13
Tricklebank, M.D.14
Saywell, K.L.15
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36
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85069099836
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The Neurotoxicity of Kainic Acid in the Culture System of Rat Hippocampal Neuron
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(a) Yamaguchi, T.; Ono, K.; Kohara, A. The Neurotoxicity of Kainic Acid in the Culture System of Rat Hippocampal Neuron. J. Neurochem. 1993, 32, 86-87.
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Yamaguchi, T.1
Ono, K.2
Kohara, A.3
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37
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85069095631
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Kainate Excitotoxicity Is Mediated by AMPA- but Not Kainate-preferring Receptors in Embryonic Rat Hippocampal Cultures
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accepted for publication
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(b) Ohno, K.; Okada, M.; Tsutsumi, R.; Kohara, A.; Yamaguchi, T. Kainate Excitotoxicity Is Mediated by AMPA-But Not Kainate-preferring Receptors in Embryonic Rat Hippocampal Cultures. Neurochem. Int. accepted for publication.
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Neurochem. Int.
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Ohno, K.1
Okada, M.2
Tsutsumi, R.3
Kohara, A.4
Yamaguchi, T.5
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38
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85069090850
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YM900 [6-(1H-imidazol-1-yl)-7-nitro-2,3(1H,4H)-quinoxalinedione] Antagonizes Non-NMDA Receptor-mediated Neurotoxicity in Rat Primary Hippocampal Cultures
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Washington DC, November
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Ono, K.; Okada, M.; Sakamoto, S.; Yamaguchi, T. YM900 [6-(1H-imidazol-1-yl)-7-nitro-2,3(1H,4H)-quinoxalinedione] Antagonizes Non-NMDA Receptor-mediated Neurotoxicity in Rat Primary Hippocampal Cultures. Presented at the 23rd Annual Meeting of the Society for Neuroscience, Washington DC, November 1993.
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(1993)
23rd Annual Meeting of the Society for Neuroscience
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Ono, K.1
Okada, M.2
Sakamoto, S.3
Yamaguchi, T.4
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39
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0030586774
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Characterization of YM90K, a Selective and Potent Antagonist of AMPA Receptors, in Rat Cortical mRNA-injected Xenopus Oocytes
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Okada, M.; Kohara, A.; Yamaguchi, T. Characterization of YM90K, a Selective and Potent Antagonist of AMPA Receptors, in Rat Cortical mRNA-injected Xenopus Oocytes. Eur. J. Pharmacol. 1996, 309, 299-306.
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Okada, M.1
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A Semiempirical Molecular Orbital Program
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Stewart, J. J. P. A Semiempirical Molecular Orbital Program. J. Comput.-Aided Mol. Des. 1990, 4, 1-105.
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Stewart, J.J.P.1
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Selective Hydrogenation of Polynitroaromatic Derivatives with Nobel Metal Catalysts in the Presence of Catalytic Amounts of Iron
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Theodoridis, G.; Manfredi, M. C.; Krebs, J. D. Selective Hydrogenation of Polynitroaromatic Derivatives with Nobel Metal Catalysts in the Presence of Catalytic Amounts of Iron. Tetrahedron Lett. 1990, 31, 43, 6141-6144.
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