-
2
-
-
58049103433
-
The history of the pharmacology and cloning of ionotropic glutamate receptors and the development of idiosyncratic nomenclature
-
Lodge, D. (2009) The history of the pharmacology and cloning of ionotropic glutamate receptors and the development of idiosyncratic nomenclature Neuropharmacology 56, 6-21
-
(2009)
Neuropharmacology
, vol.56
, pp. 6-21
-
-
Lodge, D.1
-
4
-
-
58849132420
-
Subtype Selective Kainic Acid Receptor Agonists: Discovery and Approaches to Rational Design
-
Bunch, L. and Krogsgaard-Larsen, P. (2009) Subtype Selective Kainic Acid Receptor Agonists: Discovery and Approaches to Rational Design Med. Res. Rev. 29, 3-28
-
(2009)
Med. Res. Rev.
, vol.29
, pp. 3
-
-
Bunch, L.1
Krogsgaard-Larsen, P.2
-
6
-
-
58049126584
-
A nomenclature for ligand-gated ion channels
-
Collingridge, G. L., Olsen, R. W., Peters, J., and Spedding, M. (2009) A nomenclature for ligand-gated ion channels Neuropharmacology 56, 2-5
-
(2009)
Neuropharmacology
, vol.56
, pp. 2
-
-
Collingridge, G.L.1
Olsen, R.W.2
Peters, J.3
Spedding, M.4
-
9
-
-
0026686374
-
Involvement of neurotransmitters in the nucleus tractus solitarii in cardiovascular regulation
-
van Giersbergen, P. L., Palkovits, M., and De Jong, W. (1992) Involvement of neurotransmitters in the nucleus tractus solitarii in cardiovascular regulation Physiol. Rev. 72, 789-824
-
(1992)
Physiol. Rev.
, vol.72
, pp. 789
-
-
Van Giersbergen, P.L.1
Palkovits, M.2
De Jong, W.3
-
10
-
-
0026524357
-
A glutamate receptor channel with high-affinity for domoate and kainate
-
Sommer, B., Burnashev, N., Verdoorn, T. A., Keinanen, K., Sakmann, B., and Seeburg, P. H. (1992) A glutamate receptor channel with high-affinity for domoate and kainate EMBO J. 11, 1651-1656
-
(1992)
EMBO J.
, vol.11
, pp. 1651
-
-
Sommer, B.1
Burnashev, N.2
Verdoorn, T.A.3
Keinanen, K.4
Sakmann, B.5
Seeburg, P.H.6
-
11
-
-
0033216120
-
Heteromeric kainate receptors formed by the coassembly of GluR5, GluR6, and GluR7
-
Cui, C. H. and Mayer, M. L. (1999) Heteromeric kainate receptors formed by the coassembly of GluR5, GluR6, and GluR7 J. Neurosci. 19, 8281-8291
-
(1999)
J. Neurosci.
, vol.19
, pp. 8281
-
-
Cui, C.H.1
Mayer, M.L.2
-
12
-
-
0026530085
-
The KA-2 subunit of excitatory amino-acid receptors shows widespread expression in brain and forms ion channels with distantly related subunits
-
Herb, A., Burnashev, N., Werner, P., Sakmann, B., Wisden, W., and Seeburg, P. H. (1992) The KA-2 subunit of excitatory amino-acid receptors shows widespread expression in brain and forms ion channels with distantly related subunits Neuron 8, 775-785
-
(1992)
Neuron
, vol.8
, pp. 775
-
-
Herb, A.1
Burnashev, N.2
Werner, P.3
Sakmann, B.4
Wisden, W.5
Seeburg, P.H.6
-
13
-
-
0028144152
-
Molecular cloning, expression, and pharmacological characterization of humEAA1, a human kainate receptor subunit
-
Kamboj, R. K., Schoepp, D. D., Nutt, S., Shekter, L., Korczak, B., True, R. A., Rampersad, V., Zimmerman, D. M., and Wosnick, M. A. (1994) Molecular cloning, expression, and pharmacological characterization of humEAA1, a human kainate receptor subunit J. Neurochem. 62, 1-9
-
(1994)
J. Neurochem.
, vol.62
, pp. 1
-
-
Kamboj, R.K.1
Schoepp, D.D.2
Nutt, S.3
Shekter, L.4
Korczak, B.5
True, R.A.6
Rampersad, V.7
Zimmerman, D.M.8
Wosnick, M.A.9
-
14
-
-
0027062868
-
Molecular structure and pharmacological characterization of humEAA2, a novel human kainate receptor subunit
-
Kamboj, R. K., Schoepp, D. D., Nutt, S., Shekter, L., Korczak, B., True, R. A., Zimmerman, D. M., and Wosnick, M. A. (1992) Molecular structure and pharmacological characterization of humEAA2, a novel human kainate receptor subunit Mol. Pharmacol. 42, 10-15
-
(1992)
Mol. Pharmacol.
, vol.42
, pp. 10
-
-
Kamboj, R.K.1
Schoepp, D.D.2
Nutt, S.3
Shekter, L.4
Korczak, B.5
True, R.A.6
Zimmerman, D.M.7
Wosnick, M.A.8
-
15
-
-
67650096698
-
GLUK1 receptor antagonists and hippocampal mossy fiber function
-
Nistico, R., Dargan, S., Fitzjohn, S. M., Lodge, D., Jane, D. E., Collingridge, G. L., and Bortolotto, Z. A. (2009) GLUK1 receptor antagonists and hippocampal mossy fiber function Int. Rev. Neurobiol. 85, 13-27
-
(2009)
Int. Rev. Neurobiol.
, vol.85
, pp. 13
-
-
Nistico, R.1
Dargan, S.2
Fitzjohn, S.M.3
Lodge, D.4
Jane, D.E.5
Collingridge, G.L.6
Bortolotto, Z.A.7
-
16
-
-
0032977199
-
Kainate receptors: Subunits, synaptic localization and function
-
Chittajallu, R., Braithwaite, S. P., Clarke, V. R. J., and Henley, J. M. (1999) Kainate receptors: subunits, synaptic localization and function Trends Pharmacol. Sci. 20, 26-35
-
(1999)
Trends Pharmacol. Sci.
, vol.20
, pp. 26
-
-
Chittajallu, R.1
Braithwaite, S.P.2
Clarke, V.R.J.3
Henley, J.M.4
-
17
-
-
0036244815
-
Kainate receptor agonists, antagonists and allosteric modulators
-
Bleakman, D., Gates, M. R., Ogden, A. M., and Mackowiak, M. (2002) Kainate receptor agonists, antagonists and allosteric modulators Curr. Pharm. Design 8, 873-885
-
(2002)
Curr. Pharm. Design
, vol.8
, pp. 873
-
-
Bleakman, D.1
Gates, M.R.2
Ogden, A.M.3
MacKowiak, M.4
-
18
-
-
0032192550
-
Neuropharmacology of AMPA and kainate receptors
-
Bleakman, D. and Lodge, D. (1998) Neuropharmacology of AMPA and kainate receptors Neuropharmacology 37, 1187-1204
-
(1998)
Neuropharmacology
, vol.37
, pp. 1187
-
-
Bleakman, D.1
Lodge, D.2
-
19
-
-
0034952688
-
Molecular physiology of kainate receptors
-
Lerma, J., Paternain, A. V., Rodriguez-Moreno, A., and Lopez-Garcia, J. C. (2001) Molecular physiology of kainate receptors Physiol. Rev. 81, 971-998
-
(2001)
Physiol. Rev.
, vol.81
, pp. 971
-
-
Lerma, J.1
Paternain, A.V.2
Rodriguez-Moreno, A.3
Lopez-Garcia, J.C.4
-
20
-
-
0038380386
-
Roles and rules of kainate receptors in synaptic transmission
-
Lerma, J. (2003) Roles and rules of kainate receptors in synaptic transmission Nat. Rev. Neurosci. 4, 481
-
(2003)
Nat. Rev. Neurosci.
, vol.4
, pp. 481
-
-
Lerma, J.1
-
21
-
-
26444526243
-
Kainate receptors and mossy fiber LTP
-
Bortolotto, Z. A., Nistico, R., More, J. C., Jane, D. E., and Collingridge, G. L. (2005) Kainate receptors and mossy fiber LTP Neurotoxicology 26, 769-777
-
(2005)
Neurotoxicology
, vol.26
, pp. 769
-
-
Bortolotto, Z.A.1
Nistico, R.2
More, J.C.3
Jane, D.E.4
Collingridge, G.L.5
-
22
-
-
13844266202
-
Crystal structures of the GluR5 and GluR6 ligand binding cores: Molecular mechanisms underlying kainate receptor selectivity
-
DOI 10.1016/j.neuron.2005.01.031
-
Mayer, M. L. (2005) Crystal structures of the GluR5 and GluR6 ligand binding cores: Molecular mechanisms underlying kainate receptor selectivity Neuron 45, 539-552 (Pubitemid 40249866)
-
(2005)
Neuron
, vol.45
, Issue.4
, pp. 539-552
-
-
Mayer, M.L.1
-
23
-
-
0025040913
-
Glutamate receptor channels in rat DRG neurons: Activation by kainate and quisqualate and blockade of desensitization by con A
-
DOI 10.1016/0896-6273(90)90163-A
-
Huettner, J. E. (1990) Glutamate receptor channels in rat DRG neurons: activation by kainate and quisqualate and blockade of desensitization by Con A Neuron 5, 255-266 (Pubitemid 20294977)
-
(1990)
Neuron
, vol.5
, Issue.3
, pp. 255-266
-
-
Huettner, J.E.1
-
24
-
-
34347251253
-
NMDA receptors in preBotzinger complex neurons can drive respiratory rhythm independent of AMPA receptors
-
Morgado-Valle, C. and Feldman, J. L. (2007) NMDA receptors in preBotzinger complex neurons can drive respiratory rhythm independent of AMPA receptors J.Physiol. (Oxford, U.K.) 582, 359-368
-
(2007)
J.Physiol. (Oxford, U.K.)
, vol.582
, pp. 359
-
-
Morgado-Valle, C.1
Feldman, J.L.2
-
25
-
-
2342483183
-
LY293558, a novel AMPA/GluR5 antagonist, is efficacious and well-tolerated in acute migraine
-
Sang, C. N., Ramadan, N. M., Wallihan, R. G., Chappell, A. S., Freitag, F. G., Smith, T. R., Silberstein, S. D., Johnson, K. W., Phebus, L. A., Bleakman, D., Ornstein, P. L., Arnold, B., Tepper, S. J., and Vandenhende, F. (2004) LY293558, a novel AMPA/GluR5 antagonist, is efficacious and well-tolerated in acute migraine Cephalalgia 24, 596-602
-
(2004)
Cephalalgia
, vol.24
, pp. 596
-
-
Sang, C.N.1
Ramadan, N.M.2
Wallihan, R.G.3
Chappell, A.S.4
Freitag, F.G.5
Smith, T.R.6
Silberstein, S.D.7
Johnson, K.W.8
Phebus, L.A.9
Bleakman, D.10
Ornstein, P.L.11
Arnold, B.12
Tepper, S.J.13
Vandenhende, F.14
-
26
-
-
0034059343
-
Pharmacology of AMPA/kainate receptor ligands and their therapeutic potential in neurological and psychiatric disorders
-
Lees, G. J. (2000) Pharmacology of AMPA/kainate receptor ligands and their therapeutic potential in neurological and psychiatric disorders Drugs 59, 33-78 (Pubitemid 30150572)
-
(2000)
Drugs
, vol.59
, Issue.1
, pp. 33-78
-
-
Lees, G.J.1
-
27
-
-
0031771639
-
AMPA/kainate antagonist LY293558 reduces capsaicin-evoked hyperalgesia but not pain in normal skin in humans
-
Sang, C. N., Hostetter, M. P., Gracely, R. H., Chappell, A. S., Schoepp, D. D., Lee, G., Whitcup, S., Caruso, R., and Max, M. B. (1998) AMPA/kainate antagonist LY293558 reduces capsaicin-evoked hyperalgesia but not pain in normal skin in humans Anesthesiology 89, 1060-1067
-
(1998)
Anesthesiology
, vol.89
, pp. 1060
-
-
Sang, C.N.1
Hostetter, M.P.2
Gracely, R.H.3
Chappell, A.S.4
Schoepp, D.D.5
Lee, G.6
Whitcup, S.7
Caruso, R.8
Max, M.B.9
-
28
-
-
0030770855
-
Pharmacokinetics and safety of the novel amino-3-hydroxy-5- methylisoxazole-4-propionate receptor antagonist YM90K in healthy men
-
Umemura, K., Kondo, K., Ikeda, Y., Teraya, Y., Yoshida, H., Homma, M., Uematsu, T., and Nakashima, M. (1997) Pharmacokinetics and safety of the novel amino-3-hydroxy-5-methylisoxazole-4-propionate receptor antagonist YM90K in healthy men J. Clin. Pharmacol. 37, 719-727
-
(1997)
J. Clin. Pharmacol.
, vol.37
, pp. 719
-
-
Umemura, K.1
Kondo, K.2
Ikeda, Y.3
Teraya, Y.4
Yoshida, H.5
Homma, M.6
Uematsu, T.7
Nakashima, M.8
-
29
-
-
0030858441
-
Effects of ventrolateral medullary AMPA-receptor antagonism on pressor response during muscle contraction
-
Kobayashi, T., Caringi, D., Mokler, D. J., and Ally, A. (1997) Effects of ventrolateral medullary AMPA-receptor antagonism on pressor response during muscle contraction Am. J. Physiol. Heart Circ. Physiol. 272, H2774-H2781
-
(1997)
Am. J. Physiol. Heart Circ. Physiol.
, vol.272
, pp. 2774
-
-
Kobayashi, T.1
Caringi, D.2
Mokler, D.J.3
Ally, A.4
-
30
-
-
0028821928
-
Modulation of learning-processes by ionotropic glutamate-receptor ligands
-
Danysz, W., Zajaczkowski, W., and Parsons, C. G. (1995) Modulation of learning-processes by ionotropic glutamate-receptor ligands Behav. Pharmacol. 6, 455-474
-
(1995)
Behav. Pharmacol.
, vol.6
, pp. 455
-
-
Danysz, W.1
Zajaczkowski, W.2
Parsons, C.G.3
-
31
-
-
2442657949
-
Metabotropic regulation of intrinsic excitability by synaptic activation of kainate receptors
-
Melyan, Z., Lancaster, B., and Wheal, H. V. (2004) Metabotropic regulation of intrinsic excitability by synaptic activation of kainate receptors J. Neurosci. 24, 4530-4534
-
(2004)
J. Neurosci.
, vol.24
, pp. 4530
-
-
Melyan, Z.1
Lancaster, B.2
Wheal, H.V.3
-
32
-
-
30744465646
-
Distinct subunits in heteromeric kainate receptors mediate ionotropic and metabotropic function at hippocampal mossy fiber synapses
-
Ruiz, A., Sachidhanandam, S., Utvik, J. K., Coussen, F., and Mulle, C. (2005) Distinct subunits in heteromeric kainate receptors mediate ionotropic and metabotropic function at hippocampal mossy fiber synapses J. Neurosci. 25, 11710-11718
-
(2005)
J. Neurosci.
, vol.25
, pp. 11710
-
-
Ruiz, A.1
Sachidhanandam, S.2
Utvik, J.K.3
Coussen, F.4
Mulle, C.5
-
33
-
-
0032499277
-
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice
-
Mulle, C., Sailer, A., Perez-Otano, I., Dickinson-Anson, H., Castillo, P. E., Bureau, I., Maron, C., Gage, F. H., Mann, J. R., Bettler, B., and Heinemann, S. F. (1998) Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice Nature 392, 601-605
-
(1998)
Nature
, vol.392
, pp. 601
-
-
Mulle, C.1
Sailer, A.2
Perez-Otano, I.3
Dickinson-Anson, H.4
Castillo, P.E.5
Bureau, I.6
Maron, C.7
Gage, F.H.8
Mann, J.R.9
Bettler, B.10
Heinemann, S.F.11
-
34
-
-
0031425189
-
Topical Review: Glutamate in Neurologic Diseases
-
Bittigau, P. and Ikonomidou, C. (1997) Topical Review: Glutamate in Neurologic Diseases J. Child Neurol. 12, 471-485
-
(1997)
J. Child Neurol.
, vol.12
, pp. 471
-
-
Bittigau, P.1
Ikonomidou, C.2
-
35
-
-
0030670737
-
Is High Extracellular Glutamate the Key to Excitotoxicity in Traumatic Brain Injury?
-
Obrenovitch, T. P. and Urenjak, J. (1997) Is High Extracellular Glutamate the Key to Excitotoxicity in Traumatic Brain Injury? J. Neurotrauma 14, 677-698
-
(1997)
J. Neurotrauma
, vol.14
, pp. 677
-
-
Obrenovitch, T.P.1
Urenjak, J.2
-
36
-
-
0031853680
-
Changes in the extracellular levels of glutamate and aspartate during ischemia and hypoglycemia - Effects of hypothermia
-
Boris-Moller, F. and Wieloch, T. (1998) Changes in the extracellular levels of glutamate and aspartate during ischemia and hypoglycemia-Effects of hypothermia Exp. Brain Res. 121, 277-284
-
(1998)
Exp. Brain Res.
, vol.121
, pp. 277
-
-
Boris-Moller, F.1
Wieloch, T.2
-
37
-
-
0032543142
-
Real-time measurement of ischemia-evoked glutamate release in the cerebral cortex of four and eleven vessel rat occlusion models
-
Caragine, L. P., Park, H. K., Diaz, F. G., and Phillis, J. W. (1998) Real-time measurement of ischemia-evoked glutamate release in the cerebral cortex of four and eleven vessel rat occlusion models Brain Res. 793, 255-264
-
(1998)
Brain Res.
, vol.793
, pp. 255
-
-
Caragine, L.P.1
Park, H.K.2
Diaz, F.G.3
Phillis, J.W.4
-
38
-
-
0030933984
-
Distribution of kainate receptor subunit mRNAs in human hippocampus, neocortex and cerebellum, and bilateral reduction of hippocampal GluR6 and KA2 transcripts in schizophrenia
-
Porter, R. H. P., Eastwood, S. L., and Harrison, P. J. (1997) Distribution of kainate receptor subunit mRNAs in human hippocampus, neocortex and cerebellum, and bilateral reduction of hippocampal GluR6 and KA2 transcripts in schizophrenia Brain Res. 751, 217-231
-
(1997)
Brain Res.
, vol.751
, pp. 217
-
-
Porter, R.H.P.1
Eastwood, S.L.2
Harrison, P.J.3
-
39
-
-
0029779837
-
Upregulation of spinal glutamate receptors in chronic pain
-
Harris, J. A., Corsi, M., Quartaroli, M., Arban, R., and Bentivoglio, M. (1996) Upregulation of spinal glutamate receptors in chronic pain Neuroscience 74, 7-12
-
(1996)
Neuroscience
, vol.74
, pp. 7
-
-
Harris, J.A.1
Corsi, M.2
Quartaroli, M.3
Arban, R.4
Bentivoglio, M.5
-
40
-
-
0033352862
-
AMPA receptor-PDZ interactions in facilitation of spinal sensory synapses
-
Li, P., Kerchner, G. A., Sala, C., Wei, F., Huettner, J. E., Sheng, M., and Zhuo, M. (1999) AMPA receptor-PDZ interactions in facilitation of spinal sensory synapses Nature Neurosci. 2, 972-977
-
(1999)
Nature Neurosci.
, vol.2
, pp. 972
-
-
Li, P.1
Kerchner, G.A.2
Sala, C.3
Wei, F.4
Huettner, J.E.5
Sheng, M.6
Zhuo, M.7
-
41
-
-
0032543576
-
Silent glutamatergic synapses and nociception in mammalian spinal cord
-
Li, P. and Zhuo, M. (1998) Silent glutamatergic synapses and nociception in mammalian spinal cord Nature 393, 695-698
-
(1998)
Nature
, vol.393
, pp. 695
-
-
Li, P.1
Zhuo, M.2
-
43
-
-
0037179709
-
Ethyl (3S,4aR,6S,8aR)-6-(4-ethoxycarbonylimidazol-1-ylmethyl) decahydroiso-quin oline-3-carboxylic ester: A prodrug of a GluR5 kainate receptor antagonist active in two animal models of acute migraine
-
Filla, S. A., Winter, M. A., Johnson, K. W., Bleakman, D., Bell, M. G., Bleisch, T. J., Castano, A. M., Clemens-Smith, A., del Prado, M., Dieckman, D. K., Dominguez, E., Escribano, A., Ho, K. H., Hudziak, K. J., Katofiasc, M. A., Martinez-Perez, J. A., Mateo, A., Mathes, B. M., Mattiuz, E. L., Ogden, A. M. L., Phebus, L. A., Stack, D. R., Stratford, R. E., and Ornstein, P. L. (2002) Ethyl (3S,4aR,6S,8aR)-6-(4-ethoxycarbonylimidazol-1-ylmethyl)decahydroiso-quin oline-3-carboxylic ester: A prodrug of a GluR5 kainate receptor antagonist active in two animal models of acute migraine J. Med. Chem. 45, 4383-4386
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4383
-
-
Filla, S.A.1
Winter, M.A.2
Johnson, K.W.3
Bleakman, D.4
Bell, M.G.5
Bleisch, T.J.6
Castano, A.M.7
Clemens-Smith, A.8
Del Prado, M.9
Dieckman, D.K.10
Dominguez, E.11
Escribano, A.12
Ho, K.H.13
Hudziak, K.J.14
Katofiasc, M.A.15
Martinez-Perez, J.A.16
Mateo, A.17
Mathes, B.M.18
Mattiuz, E.L.19
Ogden, A.M.L.20
Phebus, L.A.21
Stack, D.R.22
Stratford, R.E.23
Ornstein, P.L.24
more..
-
44
-
-
17744387125
-
Ionotropic and metabotropic glutamate receptor structure and pharmacology
-
Kew, J. N. C. and Kemp, J. A. (2005) Ionotropic and metabotropic glutamate receptor structure and pharmacology Psychopharmacology 179, 4-29
-
(2005)
Psychopharmacology
, vol.179
, pp. 4
-
-
Kew, J.N.C.1
Kemp, J.A.2
-
45
-
-
33750711044
-
Chemistry, biological properties and SAR analysis of quinoxalinones
-
Carta, A., Piras, S., Loriga, G., and Paglietti, G. (2006) Chemistry, biological properties and SAR analysis of quinoxalinones Mini-Rev. Med Chem 6, 1179-1200
-
(2006)
Mini-Rev. Med Chem
, vol.6
, pp. 1179
-
-
Carta, A.1
Piras, S.2
Loriga, G.3
Paglietti, G.4
-
46
-
-
0037448433
-
Competitive antagonism of AMPA receptors by ligands of different classes: Crystal structure of ATPO bound to the GluR2 ligand-binding core, in comparison with DNQX
-
Hogner, A., Greenwood, J. R., Liljefors, T., Lunn, M. L., Egebjerg, J., Larsen, I. K., Gouaux, E., and Kastrup, J. S. (2003) Competitive antagonism of AMPA receptors by ligands of different classes: Crystal structure of ATPO bound to the GluR2 ligand-binding core, in comparison with DNQX J. Med. Chem. 46, 214-221
-
(2003)
J. Med. Chem.
, vol.46
, pp. 214
-
-
Hogner, A.1
Greenwood, J.R.2
Liljefors, T.3
Lunn, M.L.4
Egebjerg, J.5
Larsen, I.K.6
Gouaux, E.7
Kastrup, J.S.8
-
47
-
-
0033636314
-
Mechanisms for activation and antagonism of an AMPA-Sensitive glutamate receptor: Crystal structures of the GluR2 ligand binding core
-
Armstrong, N. and Gouaux, E. (2000) Mechanisms for activation and antagonism of an AMPA-Sensitive glutamate receptor: Crystal structures of the GluR2 ligand binding core Neuron 28, 165-181
-
(2000)
Neuron
, vol.28
, pp. 165
-
-
Armstrong, N.1
Gouaux, E.2
-
48
-
-
0025117827
-
2,3-Dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline: A neuroprotectant for cerebral ischemia
-
Sheardown, M. J., Nielsen, E. O., Hansen, A. J., Jacobsen, P., and Honore, T. (1990) 2,3-Dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline: a neuroprotectant for cerebral ischemia Science 247, 571-574
-
(1990)
Science
, vol.247
, pp. 571
-
-
Sheardown, M.J.1
Nielsen, E.O.2
Hansen, A.J.3
Jacobsen, P.4
Honore, T.5
-
49
-
-
0029924437
-
Antagonist pharmacology of kainate- and alpha-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid-preferring receptors
-
Wilding, T. J. and Huettner, J. E. (1996) Antagonist pharmacology of kainate- and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-preferring receptors Mol. Pharmacol. 49, 540-546
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 540
-
-
Wilding, T.J.1
Huettner, J.E.2
-
50
-
-
1642296618
-
Pharmacological characterization of glutamatergic agonists and antagonists at recombinant human homomeric and heteromeric kainate receptors in vitro
-
Alt, A., Weiss, B., Ogden, A. M., Knauss, J. L., Oler, J., Ho, K., Large, T. H., and Bleakman, D. (2004) Pharmacological characterization of glutamatergic agonists and antagonists at recombinant human homomeric and heteromeric kainate receptors in vitro Neuropharmacology 46, 793-806
-
(2004)
Neuropharmacology
, vol.46
, pp. 793
-
-
Alt, A.1
Weiss, B.2
Ogden, A.M.3
Knauss, J.L.4
Oler, J.5
Ho, K.6
Large, T.H.7
Bleakman, D.8
-
51
-
-
0028607564
-
Stable expression of a functional GluR6 homomeric glutamate receptor channel in mammalian cells
-
Tygesen, C. K., Rasmussen, J. S., Jones, S. V., Hansen, A., Hansen, K., and Andersen, P. H. (1994) Stable expression of a functional GluR6 homomeric glutamate receptor channel in mammalian cells Proc. Natl. Acad. Sci. U.S.A. 91, 13018-13022
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 13018
-
-
Tygesen, C.K.1
Rasmussen, J.S.2
Jones, S.V.3
Hansen, A.4
Hansen, K.5
Andersen, P.H.6
-
52
-
-
58049104342
-
Antagonism of recombinant and native GluK3-containing kainate receptors
-
Perrais, D., Pinheiro, P. S., Jane, D. E., and Mulle, C. (2009) Antagonism of recombinant and native GluK3-containing kainate receptors Neuropharmacology 56, 131-140
-
(2009)
Neuropharmacology
, vol.56
, pp. 131
-
-
Perrais, D.1
Pinheiro, P.S.2
Jane, D.E.3
Mulle, C.4
-
53
-
-
0028618158
-
Molecular characterization of the human EAA5 (GluR7) receptor: A high-affinity kainate receptor with novel potential RNA editing sites
-
Nutt, S. L., Hoo, K. H., Rampersad, V., Deverill, R. M., Elliott, C. E., Fletcher, E. J., Adams, S. L., Korczak, B., Foldes, R. L., and Kamboj, R. K. (1994) Molecular characterization of the human EAA5 (GluR7) receptor: a high-affinity kainate receptor with novel potential RNA editing sites Recept. Channels 2, 315-326
-
(1994)
Recept. Channels
, vol.2
, pp. 315
-
-
Nutt, S.L.1
Hoo, K.H.2
Rampersad, V.3
Deverill, R.M.4
Elliott, C.E.5
Fletcher, E.J.6
Adams, S.L.7
Korczak, B.8
Foldes, R.L.9
Kamboj, R.K.10
-
54
-
-
0031862305
-
Kainate GluR5 receptor subtype mediates the nociceptive response to formalin in the rat
-
Simmons, R. M. A., Li, D. L., Hoo, K. H., Deverill, M., Ornstein, P. L., and Iyengar, S. (1998) Kainate GluR5 receptor subtype mediates the nociceptive response to formalin in the rat Neuropharmacology 37, 25-36
-
(1998)
Neuropharmacology
, vol.37
, pp. 25
-
-
Simmons, R.M.A.1
Li, D.L.2
Hoo, K.H.3
Deverill, M.4
Ornstein, P.L.5
Iyengar, S.6
-
55
-
-
0003494069
-
-
In. (, Ed.), pp - 97, 129-152, Academic Press, London
-
Nordholm, L. S. M. and Honoré, T. (1997) In Excitatory amino acids: Clinical results with antagonists. (Herrling, P. L., Ed.), pp 89 - 97, 129-152, Academic Press, London.
-
(1997)
Excitatory Amino Acids: Clinical Results with Antagonists
, pp. 89
-
-
Nordholm, L.S.M.1
Honoré, T.2
Herrling, P.L.3
-
56
-
-
0032801717
-
Pharmacological characterization of a GluR6 kainate receptor in cultured hippocampal neurons
-
Bleakman, D., Ogden, A. M., Ornstein, P. L., and Hoo, K. (1999) Pharmacological characterization of a GluR6 kainate receptor in cultured hippocampal neurons Eur. J. Pharmacol. 378, 331-337
-
(1999)
Eur. J. Pharmacol.
, vol.378
, pp. 331
-
-
Bleakman, D.1
Ogden, A.M.2
Ornstein, P.L.3
Hoo, K.4
-
57
-
-
0026532928
-
Quinoxaline derivatives - Structure-activity-relationships and physiological implications of inhibition of N-methyl-D-aspartate and non-N-methyl-D-aspartate receptor-mediated currents and synaptic potentials
-
Randle, J. C. R., Guet, T., Bobichon, C., Moreau, C., Curutchet, P., Lambolez, B., Decarvalho, L. P., Cordi, A., and Lepagnol, J. M. (1992) Quinoxaline derivatives-structure-activity-relationships and physiological implications of inhibition of N-methyl-D-aspartate and non-N-methyl-D-aspartate receptor-mediated currents and synaptic potentials Mol. Pharmacol. 41, 337-345
-
(1992)
Mol. Pharmacol.
, vol.41
, pp. 337
-
-
Randle, J.C.R.1
Guet, T.2
Bobichon, C.3
Moreau, C.4
Curutchet, P.5
Lambolez, B.6
Decarvalho, L.P.7
Cordi, A.8
Lepagnol, J.M.9
-
58
-
-
0026579124
-
Competitive inhibition by NBQX of kainate/AMPA receptor currents and excitatory synaptic potentials: Importance of 6-nitro substitution
-
Randle, J. C., Guet, T., Cordi, A., and Lepagnol, J. M. (1992) Competitive inhibition by NBQX of kainate/AMPA receptor currents and excitatory synaptic potentials: importance of 6-nitro substitution Eur. J. Pharmacol. 215, 237-244
-
(1992)
Eur. J. Pharmacol.
, vol.215
, pp. 237
-
-
Randle, J.C.1
Guet, T.2
Cordi, A.3
Lepagnol, J.M.4
-
59
-
-
0032950289
-
A new pyrrolyl-quinoxalinedione series of non-NMDA glutamate receptor antagonists: Pharmacological characterization and comparison with NBQX and valproate in the kindling model of epilepsy
-
Löscher, W., Lehmann, H., Behl, B., Seemann, D., Teschendorf, H. J., Hofmann, H. P., Lubisch, W., Höger, T., Lemaire, H. G., and Gross, G. (1999) A new pyrrolyl-quinoxalinedione series of non-NMDA glutamate receptor antagonists: pharmacological characterization and comparison with NBQX and valproate in the kindling model of epilepsy Eur. J. Neurosci. 11, 250-262
-
(1999)
Eur. J. Neurosci.
, vol.11
, pp. 250
-
-
Löscher, W.1
Lehmann, H.2
Behl, B.3
Seemann, D.4
Teschendorf, H.J.5
Hofmann, H.P.6
Lubisch, W.7
Höger, T.8
Lemaire, H.G.9
Gross, G.10
-
60
-
-
0030989187
-
Pyrrolylquinoxalinediones: The importance of pyrrolic substitution on AMPA receptor binding
-
Lubisch, W., Behl, B., and Hofmann, H. P. (1997) Pyrrolylquinoxalinediones: The importance of pyrrolic substitution on AMPA receptor binding Bioorg. Med. Chem. Lett. 7, 1101-1106
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 1101
-
-
Lubisch, W.1
Behl, B.2
Hofmann, H.P.3
-
61
-
-
0030868167
-
Pyrrolylquinoxalinediones: Dicarboxylates as highly potent AMPA receptor antagonists
-
Lubisch, W., Behl, B., Hofmann, H. P., and Teschendorf, H. J. (1997) Pyrrolylquinoxalinediones: Dicarboxylates as highly potent AMPA receptor antagonists Bioorg. Med. Chem. Lett. 7, 2441-2446
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2441
-
-
Lubisch, W.1
Behl, B.2
Hofmann, H.P.3
Teschendorf, H.J.4
-
62
-
-
0030568133
-
Pyrrolylquinoxalinediones: A new class of AMPA receptor antagonists
-
Lubisch, W., Behl, B., and Hofmann, H. P. (1996) Pyrrolylquinoxalinediones: A new class of AMPA receptor antagonists Bioorg. Med. Chem. Lett. 6, 2887-2892
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 2887
-
-
Lubisch, W.1
Behl, B.2
Hofmann, H.P.3
-
63
-
-
0034844797
-
Inhibitors of AMPA and kainate receptors
-
Madsen, U., Stensbol, T. B., and Krogsgaard-Larsen, P. (2001) Inhibitors of AMPA and kainate receptors Curr. Med. Chem. 8, 1291-1301
-
(2001)
Curr. Med. Chem.
, vol.8
, pp. 1291
-
-
Madsen, U.1
Stensbol, T.B.2
Krogsgaard-Larsen, P.3
-
64
-
-
0037135991
-
Pyrrolylquinoxalinediones carrying a piperazine residue represent highly potent and selective ligands to the homomeric kainate receptor GluR5
-
Lubisch, W., Behl, B., Henn, C., Hofmann, H. P., Reeb, J., Regner, F., and Vierling, M. (2002) Pyrrolylquinoxalinediones carrying a piperazine residue represent highly potent and selective ligands to the homomeric kainate receptor GluR5 Bioorg. Med. Chem. Lett. 12, 2113-2116
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 2113
-
-
Lubisch, W.1
Behl, B.2
Henn, C.3
Hofmann, H.P.4
Reeb, J.5
Regner, F.6
Vierling, M.7
-
65
-
-
0028169790
-
Selective block of recombinant glur6 receptors by NS-102, a novel non-NMDA receptor antagonist
-
Verdoorn, T. A., Johansen, T. H., Drejer, J., and Nielsen, E. O. (1994) Selective block of recombinant glur6 receptors by NS-102, a novel non-NMDA receptor antagonist Eur. J. Pharmacol. 269, 43-49
-
(1994)
Eur. J. Pharmacol.
, vol.269
, pp. 43
-
-
Verdoorn, T.A.1
Johansen, T.H.2
Drejer, J.3
Nielsen, E.O.4
-
66
-
-
79951834044
-
Selective displacement of low affinity tritiated kainate binding correlates with antagonism of domoic acid toxicity
-
Nielsen, E. O., Johansen, T. H., Tasker, R. A. R., Strain, S. M., Jensen, L. H., Watjen, F., and Drejer, J. (1992) Selective displacement of low affinity tritiated kainate binding correlates with antagonism of domoic acid toxicity Soc. Neurosci. Abstr. 18, 86
-
(1992)
Soc. Neurosci. Abstr.
, vol.18
, pp. 86
-
-
Nielsen, E.O.1
Johansen, T.H.2
Tasker, R.A.R.3
Strain, S.M.4
Jensen, L.H.5
Watjen, F.6
Drejer, J.7
-
67
-
-
0033550946
-
NS-257, a novel competitive AMPA receptor antagonist, interacts with kainate and NMDA receptors
-
Nijholt, I., Blank, T., Grafelmann, B., Cepok, S., Kugler, H., and Spiess, J. (1999) NS-257, a novel competitive AMPA receptor antagonist, interacts with kainate and NMDA receptors Brain Res. 821, 374-382
-
(1999)
Brain Res.
, vol.821
, pp. 374
-
-
Nijholt, I.1
Blank, T.2
Grafelmann, B.3
Cepok, S.4
Kugler, H.5
Spiess, J.6
-
68
-
-
2542439966
-
In Vitro Characterization of 5-Carboxyl-2,4-di-benzamidobenzoic Acid (NS3763), a Noncompetitive Antagonist of GLUK5 Receptors
-
Christensen, J. K., Varming, T., Ahring, P. K., Jorgensen, T. D., and Nielsen, E. O. (2004) In Vitro Characterization of 5-Carboxyl-2,4-di- benzamidobenzoic Acid (NS3763), a Noncompetitive Antagonist of GLUK5 Receptors J. Pharmacol. Exp. Ther. 309, 1003-1010
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.309
, pp. 1003
-
-
Christensen, J.K.1
Varming, T.2
Ahring, P.K.3
Jorgensen, T.D.4
Nielsen, E.O.5
-
69
-
-
33644828489
-
The Structure of a Mixed GluR2 Ligand-binding Core Dimer in Complex with (S)-Glutamate and the Antagonist (S)-NS1209
-
Kasper, C., Pickering, D. S., Mirza, O., Olsen, L., Kristensen, A. S., Greenwood, J. R., Liljefors, T., Schousboe, A., Wätjen, F., Gajhede, M., Sigurskjold, B. W., and Kastrup, J. S. (2006) The Structure of a Mixed GluR2 Ligand-binding Core Dimer in Complex with (S)-Glutamate and the Antagonist (S)-NS1209 J. Mol. Biol. 357, 1184-1201
-
(2006)
J. Mol. Biol.
, vol.357
, pp. 1184
-
-
Kasper, C.1
Pickering, D.S.2
Mirza, O.3
Olsen, L.4
Kristensen, A.S.5
Greenwood, J.R.6
Liljefors, T.7
Schousboe, A.8
Wätjen, F.9
Gajhede, M.10
Sigurskjold, B.W.11
Kastrup, J.S.12
-
70
-
-
33947188651
-
Effect of novel AMPA antagonist, NS1209, on status epilepticus: An experimental study in rat
-
Pitkänen, A., Mathiesen, C., Rønn, L. C. B., Møller, A., and Nissinen, J. (2007) Effect of novel AMPA antagonist, NS1209, on status epilepticus: An experimental study in rat Epilepsy Res. 74, 45-54
-
(2007)
Epilepsy Res.
, vol.74
, pp. 45
-
-
Pitkänen, A.1
Mathiesen, C.2
Rønn, L.C.B.3
Møller, A.4
Nissinen, J.5
-
71
-
-
63849275646
-
The Efficacy of the AMPA Receptor Antagonist NS1209 and Lidocaine in Nerve Injury Pain: A Randomized, Double-Blind, Placebo-Controlled, Three-Way Crossover Study
-
Gormsen, L., Finnerup, N. B., Almqvist, P. M., and Jensen, T. S. (2009) The Efficacy of the AMPA Receptor Antagonist NS1209 and Lidocaine in Nerve Injury Pain: A Randomized, Double-Blind, Placebo-Controlled, Three-Way Crossover Study Anesth. Analg. 108, 1311-1319
-
(2009)
Anesth. Analg.
, vol.108
, pp. 1311
-
-
Gormsen, L.1
Finnerup, N.B.2
Almqvist, P.M.3
Jensen, T.S.4
-
72
-
-
0029979667
-
Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahyd roisdoquinoline-3 carboxylic-acid
-
Bleakman, R., Schoepp, D. D., Ballyk, B., Bufton, H., Sharpe, E. F., Thomas, K., Ornstein, P. L., and Kamboj, R. K. (1996) Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahyd roisdoquinoline-3 carboxylic-acid Mol. Pharmacol. 49, 581-585
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 581
-
-
Bleakman, R.1
Schoepp, D.D.2
Ballyk, B.3
Bufton, H.4
Sharpe, E.F.5
Thomas, K.6
Ornstein, P.L.7
Kamboj, R.K.8
-
73
-
-
0027296719
-
3SR,4aRS,6RS,8aRS)-6-[2-(1H-Tetrazol-5-yl)ethyl]decahydroisoquinoline-3- carboxylic acid: A structurally novel, systemically active, competitive AMPA receptor antagonist
-
Ornstein, P. L., Arnold, M. B., Augenstein, N. K., Lodge, D., Leander, J. D., and Schoepp, D. D. (1993) 3SR,4aRS,6RS,8aRS)-6-[2-(1H-Tetrazol-5-yl)ethyl] decahydroisoquinoline-3-carboxylic acid: a structurally novel, systemically active, competitive AMPA receptor antagonist J. Med. Chem. 36, 2046-2048
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2046
-
-
Ornstein, P.L.1
Arnold, M.B.2
Augenstein, N.K.3
Lodge, D.4
Leander, J.D.5
Schoepp, D.D.6
-
74
-
-
0029122303
-
In-vitro and in vivo antagonism of AMPA receptor activation by (3S,4AR,6R,8AR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahydroisoquinoline-3 -carboxylic acid
-
Schoepp, D. D., Lodge, D., Bleakman, D., Leander, J. D., Tizzano, J. P., Wright, R. A., Palmer, A. J., Salhoff, C. R., and Ornstein, P. L. (1995) In-vitro and in vivo antagonism of AMPA receptor activation by (3S,4AR,6R,8AR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahydroisoquinoline-3 -carboxylic acid Neuropharmacology 34, 1159-1168
-
(1995)
Neuropharmacology
, vol.34
, pp. 1159
-
-
Schoepp, D.D.1
Lodge, D.2
Bleakman, D.3
Leander, J.D.4
Tizzano, J.P.5
Wright, R.A.6
Palmer, A.J.7
Salhoff, C.R.8
Ornstein, P.L.9
-
75
-
-
0030483692
-
Activity of 2,3-benzodiazepines at native rat and recombinant human glutamate receptors in vitro: Stereospecificity and selectivity profiles
-
Bleakman, D., Ballyk, B. A., Schoepp, D. D., Palmer, A. J., Bath, C. P., Sharpe, E. F., Woolley, M. L., Bufton, H. R., Kamboj, R. K., Tarnawa, I., and Lodge, D. (1996) Activity of 2,3-benzodiazepines at native rat and recombinant human glutamate receptors in vitro: Stereospecificity and selectivity profiles Neuropharmacology 35, 1689-1702
-
(1996)
Neuropharmacology
, vol.35
, pp. 1689
-
-
Bleakman, D.1
Ballyk, B.A.2
Schoepp, D.D.3
Palmer, A.J.4
Bath, C.P.5
Sharpe, E.F.6
Woolley, M.L.7
Bufton, H.R.8
Kamboj, R.K.9
Tarnawa, I.10
Lodge, D.11
-
76
-
-
0035959984
-
A structure-based design approach to the development of novel, reversible AChE inhibitors
-
Doucet-Personeni, C., Bentley, P. D., Fletcher, R. J., Kinkaid, A., Kryger, G., Pirard, B., Taylor, A., Taylor, R., Taylor, J., Viner, R., Silman, I., Sussman, J. L., Greenblatt, H. M., and Lewis, T. (2001) A structure-based design approach to the development of novel, reversible AChE inhibitors J. Med. Chem. 44, 3203-3215
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3203
-
-
Doucet-Personeni, C.1
Bentley, P.D.2
Fletcher, R.J.3
Kinkaid, A.4
Kryger, G.5
Pirard, B.6
Taylor, A.7
Taylor, R.8
Taylor, J.9
Viner, R.10
Silman, I.11
Sussman, J.L.12
Greenblatt, H.M.13
Lewis, T.14
-
77
-
-
0032701106
-
Antipsychotic-like effect of the AMPA receptor antagonist LY326325 as indicated by suppression of conditioned avoidance response in the rat
-
Mathe, J. M., Fagerquist, M. V., and Svensson, T. H. (1999) Antipsychotic-like effect of the AMPA receptor antagonist LY326325 as indicated by suppression of conditioned avoidance response in the rat J. Neural Transm. 106, 1003-1009
-
(1999)
J. Neural Transm.
, vol.106
, pp. 1003
-
-
Mathe, J.M.1
Fagerquist, M.V.2
Svensson, T.H.3
-
78
-
-
0032077972
-
The putative AMPA receptor antagonist, LY326325, produces anxiolytic-like effects without altering locomotor activity in rats
-
Kotlinska, J. and Liljequist, S. (1998) The putative AMPA receptor antagonist, LY326325, produces anxiolytic-like effects without altering locomotor activity in rats Pharmacol., Biochem. Behav. 60, 119-124
-
(1998)
Pharmacol., Biochem. Behav.
, vol.60
, pp. 119
-
-
Kotlinska, J.1
Liljequist, S.2
-
79
-
-
0033581849
-
Kainate receptors are involved in synaptic plasticity
-
Bartolotto and Clarke, Z. A. (1999) Kainate receptors are involved in synaptic plasticity Nature 402, 297
-
(1999)
Nature
, vol.402
, pp. 297
-
-
Bartolotto1
Clarke, Z.A.2
-
80
-
-
0033581849
-
Kainate receptors are involved in synaptic plasticity
-
Bortolotto, Z. A., Clarke, V. R. J., Delany, C. M., Parry, M. C., Smolders, I., Vignes, M., Ho, K. H., Miu, P., Brinton, B. T., Fantaske, R., Ogden, A., Gates, M., Ornstein, P. L., Lodge, D., Bleakman, D., and Collingridge, G. L. (1999) Kainate receptors are involved in synaptic plasticity Nature 402, 297-301
-
(1999)
Nature
, vol.402
, pp. 297
-
-
Bortolotto, Z.A.1
Clarke, V.R.J.2
Delany, C.M.3
Parry, M.C.4
Smolders, I.5
Vignes, M.6
Ho, K.H.7
Miu, P.8
Brinton, B.T.9
Fantaske, R.10
Ogden, A.11
Gates, M.12
Ornstein, P.L.13
Lodge, D.14
Bleakman, D.15
Collingridge, G.L.16
-
81
-
-
0036321170
-
Antagonists of GLU(K5)-containing kainate receptors prevent pilocarpine-induced limbic seizures
-
Smolders, I., Bortolotto, Z. A., Clarke, V. R. J., Warre, R., Khan, G. M., O'Neill, M. J., Ornstein, P. L., Bleakman, D., Ogden, A., Weiss, B., Stables, J. P., Ho, K. H., Ebinger, G., Collingridge, G. L., Lodge, D., and Michotte, Y. (2002) Antagonists of GLU(K5)-containing kainate receptors prevent pilocarpine-induced limbic seizures Nat. Neurosci. 5, 796-804
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 796
-
-
Smolders, I.1
Bortolotto, Z.A.2
Clarke, V.R.J.3
Warre, R.4
Khan, G.M.5
O'Neill, M.J.6
Ornstein, P.L.7
Bleakman, D.8
Ogden, A.9
Weiss, B.10
Stables, J.P.11
Ho, K.H.12
Ebinger, G.13
Collingridge, G.L.14
Lodge, D.15
Michotte, Y.16
-
82
-
-
34247571364
-
Anxiolytic-like effects through a GLUKS kainate receptor mechanism
-
Alt, A., Weiss, B., Ornstein, P. L., Gleason, S. D., Bleakman, D., Stratford, R. E., and Witkin, J. M. (2007) Anxiolytic-like effects through a GLUKS kainate receptor mechanism Neuropharmacology 52, 1482-1487
-
(2007)
Neuropharmacology
, vol.52
, pp. 1482
-
-
Alt, A.1
Weiss, B.2
Ornstein, P.L.3
Gleason, S.D.4
Bleakman, D.5
Stratford, R.E.6
Witkin, J.M.7
-
83
-
-
0030863091
-
A hippocampal GluR5 kainate receptor regulating inhibitory synaptic transmission
-
Clarke, V. R. J. and Ballyk, B. A. (1997) A hippocampal GluR5 kainate receptor regulating inhibitory synaptic transmission Nature 389, 599
-
(1997)
Nature
, vol.389
, pp. 599
-
-
Clarke, V.R.J.1
Ballyk, B.A.2
-
84
-
-
0032191984
-
Decahydroisoquinolines: Novel competitive AMPA/kainate antagonists with neuroprotective effects in global cerebral ischaemia
-
O'Neill, M. J., Bond, A., Ornstein, P. L., Ward, M. A., Hicks, C. A., Hoo, K., Bleakman, D., and Lodge, D. (1998) Decahydroisoquinolines: novel competitive AMPA/kainate antagonists with neuroprotective effects in global cerebral ischaemia Neuropharmacology 37, 1211-1222
-
(1998)
Neuropharmacology
, vol.37
, pp. 1211
-
-
O'Neill, M.J.1
Bond, A.2
Ornstein, P.L.3
Ward, M.A.4
Hicks, C.A.5
Hoo, K.6
Bleakman, D.7
Lodge, D.8
-
85
-
-
0032191263
-
The GluR5 subtype of kainate receptor regulates excitatory synaptic transmission in areas CA1 and CA3 of the rat hippocampus
-
Vignes, M., Clarke, V. R. J., Parry, M. J., Bleakman, D., Lodge, D., Ornstein, P. L., and Collingridge, G. L. (1998) The GluR5 subtype of kainate receptor regulates excitatory synaptic transmission in areas CA1 and CA3 of the rat hippocampus Neuropharmacology 37, 1269-1277
-
(1998)
Neuropharmacology
, vol.37
, pp. 1269
-
-
Vignes, M.1
Clarke, V.R.J.2
Parry, M.J.3
Bleakman, D.4
Lodge, D.5
Ornstein, P.L.6
Collingridge, G.L.7
-
86
-
-
33749033388
-
Antiallodynic and Antihyperalgesic Effects of Selective Competitive GLUK5 (GluR5) Ionotropic Glutamate Receptor Antagonists in the Capsaicin and Carrageenan Models in Rats
-
Jones, C. K., Alt, A., Ogden, A. M., Bleakman, D., Simmons, R. M. A., Iyengar, S., Dominguez, E., Ornstein, P. L., and Shannon, H. E. (2006) Antiallodynic and Antihyperalgesic Effects of Selective Competitive GLUK5 (GluR5) Ionotropic Glutamate Receptor Antagonists in the Capsaicin and Carrageenan Models in Rats J. Pharmacol. Exp. Ther. 319, 396-404
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.319
, pp. 396
-
-
Jones, C.K.1
Alt, A.2
Ogden, A.M.3
Bleakman, D.4
Simmons, R.M.A.5
Iyengar, S.6
Dominguez, E.7
Ornstein, P.L.8
Shannon, H.E.9
-
87
-
-
33746027410
-
Pharmacological characterization of the competitive GLU(K5) receptor antagonist decahydroisoquinoline LY466195 in vitro and in vivo
-
Weiss, B., Alt, A., Ogden, A. M., Gates, M., Dieckman, D. K., Clemens-Smith, A., Ho, K. H., Jarvie, K., Rizkalla, G., Wright, R. A., Calligaro, D. O., Schoepp, D., Mattiuz, E. L., Stratford, R. E., Johnson, B., Salhoff, C., Katofiasc, M., Phebus, L. A., Schenck, K., Cohen, M., Filla, S. A., Ornstein, P. L., Johnson, K. W., and Bleakman, D. (2006) Pharmacological characterization of the competitive GLU(K5) receptor antagonist decahydroisoquinoline LY466195 in vitro and in vivo J. Pharmacol. Exp. Ther. 318, 772-781
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.318
, pp. 772
-
-
Weiss, B.1
Alt, A.2
Ogden, A.M.3
Gates, M.4
Dieckman, D.K.5
Clemens-Smith, A.6
Ho, K.H.7
Jarvie, K.8
Rizkalla, G.9
Wright, R.A.10
Calligaro, D.O.11
Schoepp, D.12
Mattiuz, E.L.13
Stratford, R.E.14
Johnson, B.15
Salhoff, C.16
Katofiasc, M.17
Phebus, L.A.18
Schenck, K.19
Cohen, M.20
Filla, S.A.21
Ornstein, P.L.22
Johnson, K.W.23
Bleakman, D.24
more..
-
88
-
-
77649300068
-
LY466195, a clinically active compound in the acute treatment of migraine, inhibits activation in the trigeminocervical complex and the ventroposteromedial thalamus after nociceptive trigeminovascular activation
-
Andreou, A. P. and Goadsby, P. J. (2009) LY466195, a clinically active compound in the acute treatment of migraine, inhibits activation in the trigeminocervical complex and the ventroposteromedial thalamus after nociceptive trigeminovascular activation Cephalalgia 29, 132-132
-
(2009)
Cephalalgia
, vol.29
, pp. 132
-
-
Andreou, A.P.1
Goadsby, P.J.2
-
89
-
-
0027715150
-
Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin A
-
Partin, K. M., Patneau, D. K., Winters, C. A., Mayer, M. L., and Buonanno, A. (1993) Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin A Neuron 11, 1069-1082
-
(1993)
Neuron
, vol.11
, pp. 1069
-
-
Partin, K.M.1
Patneau, D.K.2
Winters, C.A.3
Mayer, M.L.4
Buonanno, A.5
-
90
-
-
21244432731
-
Two Prodrugs of Potent and Selective GluR5 Kainate Receptor Antagonists Actives in Three Animal Models of Pain
-
Dominguez, E., Iyengar, S., Shannon, H. E., Bleakman, D., Alt, A., Arnold, B. M., Bell, M. G., Bleisch, T. J., Buckmaster, J. L., Castano, A. M., Del Prado, M., Escribano, A., Filla, S. A., Ho, K. H., Hudziak, K. J., Jones, C. K., Martinez-Perez, J. A., Mateo, A., Mathes, B. M., Mattiuz, E. L., Ogden, A. M. L., Simmons, R. M. A., Stack, D. R., Stratford, R. E., Winter, M. A., Wu, Z., and Ornstein, P. L. (2005) Two Prodrugs of Potent and Selective GluR5 Kainate Receptor Antagonists Actives in Three Animal Models of Pain J. Med. Chem. 48, 4200-4203
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4200
-
-
Dominguez, E.1
Iyengar, S.2
Shannon, H.E.3
Bleakman, D.4
Alt, A.5
Arnold, B.M.6
Bell, M.G.7
Bleisch, T.J.8
Buckmaster, J.L.9
Castano, A.M.10
Del Prado, M.11
Escribano, A.12
Filla, S.A.13
Ho, K.H.14
Hudziak, K.J.15
Jones, C.K.16
Martinez-Perez, J.A.17
Mateo, A.18
Mathes, B.M.19
Mattiuz, E.L.20
Ogden, A.M.L.21
Simmons, R.M.A.22
Stack, D.R.23
Stratford, R.E.24
Winter, M.A.25
Wu, Z.26
Ornstein, P.L.27
more..
-
91
-
-
34147135568
-
Synthesis and Pharmacological Characterization of N3-Substituted Willardiine Derivatives: Role of the Substituent at the 5-Position of the Uracil Ring in the Development of Highly Potent and Selective GLUK5 Kainate Receptor Antagonists
-
Dolman, N. P., More, J. C. A., Alt, A., Knauss, J. L., Pentikäinen, O. T., Glasser, C. R., Bleakman, D., Mayer, M. L., Collingridge, G. L., and Jane, D. E. (2007) Synthesis and Pharmacological Characterization of N3-Substituted Willardiine Derivatives: Role of the Substituent at the 5-Position of the Uracil Ring in the Development of Highly Potent and Selective GLUK5 Kainate Receptor Antagonists J. Med. Chem. 50, 1558-1570
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1558
-
-
Dolman, N.P.1
More, J.C.A.2
Alt, A.3
Knauss, J.L.4
Pentikäinen, O.T.5
Glasser, C.R.6
Bleakman, D.7
Mayer, M.L.8
Collingridge, G.L.9
Jane, D.E.10
-
92
-
-
33646134848
-
Structure-Activity Relationship Studies on N3-Substituted Willardiine Derivatives Acting as AMPA or Kainate Receptor Antagonists
-
Dolman, N. P., More, J. C. A., Alt, A., Knauss, J. L., Troop, H. M., Bleakman, D., Collingridge, G. L., and Jane, D. E. (2006) Structure-Activity Relationship Studies on N3-Substituted Willardiine Derivatives Acting as AMPA or Kainate Receptor Antagonists J. Med. Chem. 49, 2579-2592
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2579
-
-
Dolman, N.P.1
More, J.C.A.2
Alt, A.3
Knauss, J.L.4
Troop, H.M.5
Bleakman, D.6
Collingridge, G.L.7
Jane, D.E.8
-
93
-
-
2542422824
-
Characterisation of UBP296: A novel, potent and selective kainate receptor antagonist
-
More, J. C. A., Nistico, R., Dolman, N. P., Clarke, V. R. J., Alt, A. J., Ogden, A. M., Buelens, F. P., Troop, H. M., Kelland, E. E., Pilato, F., Bleakman, D., Bortolotto, Z. A., Collingridge, G. L., and Jane, D. E. (2004) Characterisation of UBP296: a novel, potent and selective kainate receptor antagonist Neuropharmacology 47, 46-64
-
(2004)
Neuropharmacology
, vol.47
, pp. 46
-
-
More, J.C.A.1
Nistico, R.2
Dolman, N.P.3
Clarke, V.R.J.4
Alt, A.J.5
Ogden, A.M.6
Buelens, F.P.7
Troop, H.M.8
Kelland, E.E.9
Pilato, F.10
Bleakman, D.11
Bortolotto, Z.A.12
Collingridge, G.L.13
Jane, D.E.14
-
94
-
-
33645321641
-
Glutamate receptors at atomic resolution
-
Mayer, M. L. (2006) Glutamate receptors at atomic resolution Nature 440, 456-462
-
(2006)
Nature
, vol.440
, pp. 456-462
-
-
Mayer, M.L.1
-
95
-
-
28244465987
-
Synthesis and pharmacology of willardiine derivatives acting as antagonists of kainate receptors
-
Dolman, N. P., Troop, H. M., More, J. C., Alt, A., Knauss, J. L., Nistico, R., Jack, S., Morley, R. M., Bortolotto, Z. A., Roberts, P. J., Bleakman, D., Collingridge, G. L., and Jane, D. E. (2005) Synthesis and pharmacology of willardiine derivatives acting as antagonists of kainate receptors J. Med. Chem. 48, 7867-7881
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7867
-
-
Dolman, N.P.1
Troop, H.M.2
More, J.C.3
Alt, A.4
Knauss, J.L.5
Nistico, R.6
Jack, S.7
Morley, R.M.8
Bortolotto, Z.A.9
Roberts, P.J.10
Bleakman, D.11
Collingridge, G.L.12
Jane, D.E.13
-
96
-
-
0036898034
-
The novel antagonist 3-CBW discriminates between kainate receptors expressed on neonatal rat motoneurones and those on dorsal root C-fibres
-
More, J. C. A., Troop, H. M., and Jane, D. E. (2002) The novel antagonist 3-CBW discriminates between kainate receptors expressed on neonatal rat motoneurones and those on dorsal root C-fibres Br. J. Pharmacol. 137, 1125-1133
-
(2002)
Br. J. Pharmacol.
, vol.137
, pp. 1125
-
-
More, J.C.A.1
Troop, H.M.2
Jane, D.E.3
-
97
-
-
66149128065
-
Mechanisms of Antagonism of the GluR2 AMPA Receptor: Structure and Dynamics of the Complex of Two Willardiine Antagonists with the Glutamate Binding Domain
-
Ahmed, A. H., Thompson, M. D., Fenwick, M. K., Romero, B., Loh, A. P., Jane, D. E., Sondermann, H., and Oswald, R. E. (2009) Mechanisms of Antagonism of the GluR2 AMPA Receptor: Structure and Dynamics of the Complex of Two Willardiine Antagonists with the Glutamate Binding Domain Biochemistry 48, 3894-3903
-
(2009)
Biochemistry
, vol.48
, pp. 3894
-
-
Ahmed, A.H.1
Thompson, M.D.2
Fenwick, M.K.3
Romero, B.4
Loh, A.P.5
Jane, D.E.6
Sondermann, H.7
Oswald, R.E.8
-
98
-
-
0037362504
-
Structural requirements for novel willardiine derivatives acting as AMPA and kainate receptor antagonists
-
More, J. C. A., Troop, H. M., Dolman, N. P., and Jane, D. E. (2003) Structural requirements for novel willardiine derivatives acting as AMPA and kainate receptor antagonists Br. J. Pharmacol. 138, 1093
-
(2003)
Br. J. Pharmacol.
, vol.138
, pp. 1093
-
-
More, J.C.A.1
Troop, H.M.2
Dolman, N.P.3
Jane, D.E.4
-
99
-
-
33847421781
-
Inhibition of kainate receptors reduces the frequency of hippocampal theta oscillations
-
Huxter, J. R., Zinyuk, L. E., Roloff, E. V. L., Clarke, V. R. J., Dolman, N. P., More, J. C. A., Jane, D. E., Collingridge, G. L., and Muller, R. U. (2007) Inhibition of kainate receptors reduces the frequency of hippocampal theta oscillations J. Neurosci. 27, 2212-2223
-
(2007)
J. Neurosci.
, vol.27
, pp. 2212
-
-
Huxter, J.R.1
Zinyuk, L.E.2
Roloff, E.V.L.3
Clarke, V.R.J.4
Dolman, N.P.5
More, J.C.A.6
Jane, D.E.7
Collingridge, G.L.8
Muller, R.U.9
-
100
-
-
58049127893
-
ACET is a highly potent and specific kainate receptor antagonist: Characterisation and effects on hippocampal mossy fibre function
-
Dargan, S. L., Clarke, V. R. J., Alushin, G. M., Sherwood, J. L., Nistico, R., Bortolotto, Z. A., Ogden, A. M., Bleakman, D., Doherty, A. J., Lodge, D., Mayer, M. L., Fitzjohn, S. M., Jane, D. E., and Collingridge, G. L. (2009) ACET is a highly potent and specific kainate receptor antagonist: Characterisation and effects on hippocampal mossy fibre function Neuropharmacology 56, 121-130
-
(2009)
Neuropharmacology
, vol.56
, pp. 121
-
-
Dargan, S.L.1
Clarke, V.R.J.2
Alushin, G.M.3
Sherwood, J.L.4
Nistico, R.5
Bortolotto, Z.A.6
Ogden, A.M.7
Bleakman, D.8
Doherty, A.J.9
Lodge, D.10
Mayer, M.L.11
Fitzjohn, S.M.12
Jane, D.E.13
Collingridge, G.L.14
-
101
-
-
58049096661
-
Kainate receptors: Pharmacology, function and therapeutic potential
-
Jane, D. E., Lodge, D., and Collingridge, G. L. (2009) Kainate receptors: Pharmacology, function and therapeutic potential Neuropharmacology 56, 90-113
-
(2009)
Neuropharmacology
, vol.56
, pp. 90
-
-
Jane, D.E.1
Lodge, D.2
Collingridge, G.L.3
-
102
-
-
79951847471
-
Discovery of a New Class of Ionotropic Glutamate Receptor Antagonists by the Rational Design of (2 S,3 R)-3-(3-Carboxyphenyl)-pyrrolidine-2-carboxylic Acid
-
DOI: 10.1021/cn100093f
-
Larsen, A. M., Venskutonyté, R., Nielsen, B., Pickering, D. S., and Bunch, L. (2010) Discovery of a New Class of Ionotropic Glutamate Receptor Antagonists by the Rational Design of (2 S,3 R)-3-(3-Carboxyphenyl)-pyrrolidine- 2-carboxylic Acid, ACS Chem. Neurosci. DOI: 10.1021/cn100093f.
-
(2010)
ACS Chem. Neurosci.
-
-
Larsen, A.M.1
Venskutonyté, R.2
Nielsen, B.3
Pickering, D.S.4
Bunch, L.5
-
103
-
-
0033618477
-
Asymmetric synthesis of some substituted-3-phenyl prolines
-
Micheli, F., Di Fabio, R., and Marchioro, C. (1999) Asymmetric synthesis of some substituted-3-phenyl prolines Farmaco 54, 461-464
-
(1999)
Farmaco
, vol.54
, pp. 461
-
-
Micheli, F.1
Di Fabio, R.2
Marchioro, C.3
-
104
-
-
0032731808
-
Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5- tert -butyl-3-(phosphonomethoxy)-4- isoxazolyl]propionic acid
-
Moller, E. H., Egebjerg, J., Brehm, L., Stensbol, T. B., Johansen, T. N., Madsen, U., and Krogsgaard-Larsen, P. (1999) Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5- tert -butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid Chirality 11, 752-759
-
(1999)
Chirality
, vol.11
, pp. 752
-
-
Moller, E.H.1
Egebjerg, J.2
Brehm, L.3
Stensbol, T.B.4
Johansen, T.N.5
Madsen, U.6
Krogsgaard-Larsen, P.7
-
105
-
-
34548512475
-
Partial agonism and antagonism of the ionotropic glutamate receptor iGLuR5 - Structures of the ligand-binding core in complex with domoic acid and 2-amino-3-[5- tert -butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid
-
Hald, H., Naur, P., Pickering, D. S., Sprogoe, D., Madsen, U., Timmermann, D. B., Ahring, P. K., Liljefors, T., Schousboe, A., Egebjerg, J., Gajhede, M., and Kastrup, J. S. (2007) Partial agonism and antagonism of the ionotropic glutamate receptor iGLuR5-Structures of the ligand-binding core in complex with domoic acid and 2-amino-3-[5- tert -butyl-3-(phosphonomethoxy)-4- isoxazolyl]propionic acid J. Biol. Chem. 282, 25726-25736
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 25726
-
-
Hald, H.1
Naur, P.2
Pickering, D.S.3
Sprogoe, D.4
Madsen, U.5
Timmermann, D.B.6
Ahring, P.K.7
Liljefors, T.8
Schousboe, A.9
Egebjerg, J.10
Gajhede, M.11
Kastrup, J.S.12
-
106
-
-
68649117410
-
3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands
-
Szymanska, E., Pickering, D. S., Nielsen, B., and Johansen, T. N. (2009) 3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands Bioorg. Med. Chem. 17, 6390-6401
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6390
-
-
Szymanska, E.1
Pickering, D.S.2
Nielsen, B.3
Johansen, T.N.4
-
107
-
-
0031965689
-
Antagonist properties of a phosphono isoxazole amino acid at glutamate R1-4 (R, S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid receptor subtypes
-
Wahl, P., Anker, C., Traynelis, S. F., Egebjerg, J., Rasmussen, J. S., Krogsgaard-Larsen, P., and Madsen, U. (1998) Antagonist properties of a phosphono isoxazole amino acid at glutamate R1-4 (R, S)-2-amino-3-(3-hydroxy-5- methyl-4-isoxazolyl)propionic acid receptor subtypes Mol. Pharmacol. 53, 590-596
-
(1998)
Mol. Pharmacol.
, vol.53
, pp. 590
-
-
Wahl, P.1
Anker, C.2
Traynelis, S.F.3
Egebjerg, J.4
Rasmussen, J.S.5
Krogsgaard-Larsen, P.6
Madsen, U.7
-
108
-
-
0021965017
-
Depressant Actions of Gamma-D-Glutamylaminomethyl Sulfonate (Gams) on Amino Acid-Induced and Synaptic Excitation in the Cat Spinal-Cord
-
Davies, J. and Watkins, J. C. (1985) Depressant Actions of Gamma-D-Glutamylaminomethyl Sulfonate (Gams) on Amino Acid-Induced and Synaptic Excitation in the Cat Spinal-Cord Brain Res. 327, 113-120
-
(1985)
Brain Res.
, vol.327
, pp. 113
-
-
Davies, J.1
Watkins, J.C.2
-
109
-
-
0021688291
-
Phosphono dipeptides and piperazine derivatives as antagonists of amino acid-included and synaptic excitation in mammalian and amphibian spinal-cord
-
Davies, J., Jones, A. W., Sheardown, M. J., Smith, D. A. S., and Watkins, J. C. (1984) Phosphono dipeptides and piperazine derivatives as antagonists of amino acid-included and synaptic excitation in mammalian and amphibian spinal-cord Neurosci. Lett. 52, 79-84
-
(1984)
Neurosci. Lett.
, vol.52
, pp. 79
-
-
Davies, J.1
Jones, A.W.2
Sheardown, M.J.3
Smith, D.A.S.4
Watkins, J.C.5
-
111
-
-
0026596597
-
Signal transduction and pharmacological characteristics of a metabotropic glutamate receptor, mGluR1, in transfected CHO cells
-
Aramori, I. and Nakanishi, S. (1992) Signal transduction and pharmacological characteristics of a metabotropic glutamate receptor, mGluR1, in transfected CHO cells Neuron 8, 757-765
-
(1992)
Neuron
, vol.8
, pp. 757
-
-
Aramori, I.1
Nakanishi, S.2
-
112
-
-
0027183405
-
Gamma-D-glutamylaminomethyl sulfonic-acid (GAMS) distinguishes kainic acid-induced from AMPA-induced responses in xenopus-oocytes expressing chick brain glutamate receptors
-
Zhou, N., Hammerland, L. G., and Parks, T. N. (1993) Gamma-D- glutamylaminomethyl sulfonic-acid (GAMS) distinguishes kainic acid-induced from AMPA-induced responses in xenopus-oocytes expressing chick brain glutamate receptors Neuropharmacology 32, 767-775
-
(1993)
Neuropharmacology
, vol.32
, pp. 767
-
-
Zhou, N.1
Hammerland, L.G.2
Parks, T.N.3
-
113
-
-
0022912434
-
Parallel antagonism of synaptic transmission and kainate/quisqualate responses in the hippocampus by piperazine-2,3-dicarboxylic acid analogs
-
Ganong, A. H., Jones, A. W., Watkins, J. C., and Cotman, C. W. (1986) Parallel antagonism of synaptic transmission and kainate/quisqualate responses in the hippocampus by piperazine-2,3-dicarboxylic acid analogs J. Neurosci. 6, 930-937
-
(1986)
J. Neurosci.
, vol.6
, pp. 930
-
-
Ganong, A.H.1
Jones, A.W.2
Watkins, J.C.3
Cotman, C.W.4
-
114
-
-
0023180475
-
A comparison of excitatory amino-acid antagonists acting at primary afferent c-fibers and motoneurons of the isolated spinal-cord of the rat
-
Evans, R. H., Evans, S. J., Pook, P. C., and Sunter, D. C. (1987) A comparison of excitatory amino-acid antagonists acting at primary afferent c-fibers and motoneurons of the isolated spinal-cord of the rat Br. J. Pharmacol. 91, 531-537
-
(1987)
Br. J. Pharmacol.
, vol.91
, pp. 531
-
-
Evans, R.H.1
Evans, S.J.2
Pook, P.C.3
Sunter, D.C.4
-
115
-
-
0027486072
-
Neuropharmacology of quinolinic and kynurenic acids
-
Stone, T. W. (1993) Neuropharmacology of quinolinic and kynurenic acids Pharmacol. Rev. 45, 309-379 (Pubitemid 23292874)
-
(1993)
Pharmacological Reviews
, vol.45
, Issue.3
, pp. 309-379
-
-
Stone, T.W.1
-
116
-
-
14444285260
-
Novel Systemically Active Antagonists of the Glycine Site of the N-Methyl-D-aspartate Receptor: Electrophysiological, Biochemical and Behavioral Characterization
-
Parsons, C. G., Danysz, W., Quack, G. n., Hartmann, S., Lorenz, B., Wollenburg, C., Baran, L., Przegalinski, E., Kostowski, W., Krzascik, P., Chizh, B., and Max. Headley, P. (1997) Novel Systemically Active Antagonists of the Glycine Site of the N-Methyl-D-aspartate Receptor: Electrophysiological, Biochemical and Behavioral Characterization J. Pharmacol. Exp. Ther. 283, 1264-1275
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.283
, pp. 1264
-
-
Parsons, C.G.1
Danysz, W.2
Quack, G.N.3
Hartmann, S.4
Lorenz, B.5
Wollenburg, C.6
Baran, L.7
Przegalinski, E.8
Kostowski, W.9
Krzascik, P.10
Chizh, B.11
Max. Headley, P.12
-
117
-
-
0024564076
-
A glycine site associated with N-methyl-D-aspartic acid receptors: Characterization and identification of a new class of antagonists
-
Kessler, M., Terramani, T., and Lynch, G. (1989) A glycine site associated with N-methyl-D-aspartic acid receptors: characterization and identification of a new class of antagonists J. Neurochem. 52, 1319-1328
-
(1989)
J. Neurochem.
, vol.52
, pp. 1319
-
-
Kessler, M.1
Terramani, T.2
Lynch, G.3
-
118
-
-
59149090373
-
Pharmacological Manipulation of Kynurenic Acid: Potential in the Treatment of Psychiatric Disorders
-
Erhardt, S., Olsson, S. K., and Engberg, G. r. (2009) Pharmacological Manipulation of Kynurenic Acid: Potential in the Treatment of Psychiatric Disorders CNS Drugs 23, 91-101
-
(2009)
CNS Drugs
, vol.23
, pp. 91
-
-
Erhardt, S.1
Olsson, S.K.2
Engberg, G.R.3
|