-
1
-
-
0032912771
-
The glutamate receptor ion channels
-
DINGLEDINE R, BORGES K, BOWIE D, TRAYNELIS SF: The glutamate receptor ion channels. Pharmacol. Rev. (1999) 51(1):7-61.
-
(1999)
Pharmacol. Rev.
, vol.51
, Issue.1
, pp. 7-61
-
-
Dingledine, R.1
Borges, K.2
Bowie, D.3
Traynelis, S.F.4
-
3
-
-
0034059343
-
Pharmacology of AMPA/kainate receptor ligands and their therapeutic potential in neurological and psychiatric disorders
-
LEES GJ: Pharmacology of AMPA/kainate receptor ligands and their therapeutic potential in neurological and psychiatric disorders. Drugs (2000) 59 (1):33-78.
-
(2000)
Drugs
, vol.59
, Issue.1
, pp. 33-78
-
-
Lees, G.J.1
-
4
-
-
0037025273
-
The pharmacological manipulation of glutamate receptors and neuroprotection
-
STONE TW, ADDAE JI: The pharmacological manipulation of glutamate receptors and neuroprotection. Eur. J. Pharmacol. (2002) 447(2-3):285-296.
-
(2002)
Eur. J. Pharmacol.
, vol.447
, Issue.2-3
, pp. 285-296
-
-
Stone, T.W.1
Addae, J.I.2
-
5
-
-
0032486422
-
The tetrameric structure of a glutamate receptor channel
-
ROSENMUND C, STERN-BACH Y, STEVENS CF: The tetrameric structure of a glutamate receptor channel. Science (1998) 280(5369):1596-1599.
-
(1998)
Science
, vol.280
, Issue.5369
, pp. 1596-1599
-
-
Rosenmund, C.1
Stern-Bach, Y.2
Stevens, C.F.3
-
6
-
-
0029966280
-
Three-dimensional models of non-NMDA glutamate receptors
-
SUTCLIFFE MJ, WO ZG, OSWALD RE: Three-dimensional models of non-NMDA glutamate receptors. Biophys. J. (1996) 70(4):1575-1589.
-
(1996)
Biophys. J.
, vol.70
, Issue.4
, pp. 1575-1589
-
-
Sutcliffe, M.J.1
Wo, Z.G.2
Oswald, R.E.3
-
7
-
-
0031690238
-
Three-dimensional models of glutamate receptors
-
SUTCLIFFE MJ, SMEETON AH, WO ZG, OSWALD RE: Three-dimensional models of glutamate receptors. Biochem. Soc. Trans. (1998) 26(3):450-458.
-
(1998)
Biochem. Soc. Trans.
, vol.26
, Issue.3
, pp. 450-458
-
-
Sutcliffe, M.J.1
Smeeton, A.H.2
Wo, Z.G.3
Oswald, R.E.4
-
8
-
-
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 JR, LILJEFORS T et al.: 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. (2003) 46(2):214-221.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.2
, pp. 214-221
-
-
Hogner, A.1
Greenwood, J.R.2
Liljefors, T.3
-
9
-
-
0033636314
-
Mechanisms for activation and antagonism of an AMPA-sensitive glutamate receptor: Crystal structures of the GluR2 ligand binding core
-
ARMSTRONG N, GOUAUX E: Mechanisms for activation and antagonism of an AMPA-sensitive glutamate receptor: crystal structures of the GluR2 ligand binding core. Neuron (2000) 28(1):165-181.
-
(2000)
Neuron
, vol.28
, Issue.1
, pp. 165-181
-
-
Armstrong, N.1
Gouaux, E.2
-
11
-
-
0037167777
-
Novel quinolinone-phosphonic acid AMPA antagonists devoid of nephrotoxicity
-
CORDI AA, DESOS P, RUANO E et al.: Novel quinolinone-phosphonic acid AMPA antagonists devoid of nephrotoxicity. Farmaco, (2002) 57(10):787-802.
-
(2002)
Farmaco
, vol.57
, Issue.10
, pp. 787-802
-
-
Cordi, A.A.1
Desos, P.2
Ruano, E.3
-
12
-
-
0035860311
-
A potent AMPA/kainate receptor antagonist, YM-90K, attenuates the loss of N-acetylaspartate in the hippocampal CA1 area after transient unilateral forebrain ischemia in gerbils
-
NAKANO M, UEDA H, LI JY, MATSUMOTO M, YANAGIHARA T A potent AMPA/kainate receptor antagonist, YM-90K, attenuates the loss of N-acetylaspartate in the hippocampal CA1 area after transient unilateral forebrain ischemia in gerbils. Life Sci. (2001) 69(17):1983-1990.
-
(2001)
Life Sci.
, vol.69
, Issue.17
, pp. 1983-1990
-
-
Nakano, M.1
Ueda, H.2
Li, J.Y.3
Matsumoto, M.4
Yanagihara, T.5
-
14
-
-
13144306063
-
ZK-200775: A phosphonate quinoxalinedione AMPA antagonist for neuroprotection in stroke and trauma
-
TURSKI L, HUTH A, SHEARDOWN M et al.: ZK-200775: a phosphonate quinoxalinedione AMPA antagonist for neuroprotection in stroke and trauma. Proc. Natl. Acad. Sci. USA (1998) 95(18):10960-10965.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, Issue.18
, pp. 10960-10965
-
-
Turski, L.1
Huth, A.2
Sheardown, M.3
-
15
-
-
0036904876
-
AMPA antagonist ZK200775 in patients with acute ischemic stroke: Possible glial cell toxicity detected by monitoring of S-100B serum levels
-
ELTING JW SULTER GA, KASTE M et al.: AMPA antagonist ZK200775 in patients with acute ischemic stroke: possible glial cell toxicity detected by monitoring of S-100B serum levels. Stroke (2002) 33(12):2813-2818.
-
(2002)
Stroke
, vol.33
, Issue.12
, pp. 2813-2818
-
-
Elting, J.W.1
Sulter, G.A.2
Kaste, M.3
-
17
-
-
0141851403
-
Synthesis and AMPA receptor antagonistic activity of a novel class of quinoxalinecarboxylic acid with a substituted phenyl group at the C-7 position
-
TAKANO Y, SHIGA F, ASANO J, ANDO N, UCHIKI H, ANRAKU T Synthesis and AMPA receptor antagonistic activity of a novel class of quinoxalinecarboxylic acid with a substituted phenyl group at the C-7 position. Bioorg. Med Chem. Lett(2003) 13(20):3521-3525.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, Issue.20
, pp. 3521-3525
-
-
Takano, Y.1
Shiga, F.2
Asano, J.3
Ando, N.4
Uchiki, H.5
Anraku, T.6
-
18
-
-
0033048804
-
Synthesis, glycine/NMDA and AMPA binding activity of some new 2,5,6-trioxopyrazino[1,2,3-de]quinoxalines and of their restricted analogs 2,5-dioxo- and 4,5-(dioxoimidazo[1,5,4-de]quinoxalines
-
VARANO F, CATARZI D, COLOTTA V et al.: Synthesis, glycine/NMDA and AMPA binding activity of some new 2,5,6-trioxopyrazino[1,2,3-de]quinoxalines and of their restricted analogs 2,5-dioxo- and 4,5-(dioxoimidazo[1,5,4-de]quinoxalines.Arch. Pharm. (Weinheim) (1999) 332(6):201-207.
-
(1999)
Arch. Pharm. (Weinheim)
, vol.332
, Issue.6
, pp. 201-207
-
-
Varano, F.1
Catarzi, D.2
Colotta, V.3
-
19
-
-
0034687251
-
7-Chloro-4,5-dihydro,-8-(1,2,4-triazol-4-yl)-4-oxo-1,2,4-triazolo[l, 5-a]quinoxaline-2-carboxylates as novel highly selective AMPA receptor antagonists
-
CATARZI D, COLOTTA V, VARANO F et al: 7-Chloro-4,5-dihydro,-8-(1,2,4-triazol-4-yl)-4-oxo-1,2,4-triazolo[l, 5-a]quinoxaline-2-carboxylates as novel highly selective AMPA receptor antagonists. J. Med. Chem. (2000) 43(21):3824-3826.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.21
, pp. 3824-3826
-
-
Catarzi, D.1
Colotta, V.2
Varano, F.3
-
20
-
-
0035855816
-
Synthesis, ionotropic glutamate receptor binding affinity, and structure-activity relationships of a new set of 4,5-dihydro-8-heteroaryl-4-oxo-1,2,4-triazolo[1,5-a]quinoxaline-2- carboxylates analogues of TQX-173
-
CATARZI D, COLOTTA V, VARANO F et al.: Synthesis, ionotropic glutamate receptor binding affinity, and structure-activity relationships of a new set of 4,5-dihydro-8-heteroaryl-4-oxo-1,2,4-triazolo [1,5-a]quinoxaline-2-carboxylates analogues of TQX-173. J. Med. Chem. (2001) 44 (19):3157-3165.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.19
, pp. 3157-3165
-
-
Catarzi, D.1
Colotta, V.2
Varano, F.3
-
21
-
-
0346100347
-
Synthesis and biological evaluation of analogues of 7-chloro-4,5-dihydro-4-oxo-8-(1,2,4-triazol-4-yl)-1,2,4- triazolo[1,5-a]quinoxaline-2-carboxylic acid (TQX-173) as novel selective AMPA receptor antagonists
-
CATARZI D, COLOTTA V, VARANO F et al.: Synthesis and biological evaluation of analogues of 7-chloro-4,5-dihydro-4- oxo-8-(1,2,4-triazol-4-yl)-1,2,4-triazolo[1,5-a]quinoxaline- 2-carboxylic acid (TQX-173) as novel selective AMPA receptor antagonists. J. Med. Chem. (2004) 47(1):262-272.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.1
, pp. 262-272
-
-
Catarzi, D.1
Colotta, V.2
Varano, F.3
-
22
-
-
0037186487
-
Synthesis and biological evaluation of a new set of pyrazolo[1,5-c]quinazoline-2-carboxylates as novel excitatory amino acid antagonists
-
VARANO F, CATARZI D, COLOTTA V et al.: Synthesis and biological evaluation of a new set of pyrazolo[1,5-c]quinazoline-2-carboxylates as novel excitatory amino acid antagonists. J. Med. Chem. (2002) 45(5):1035-1044.
-
(2002)
J. Med. Chem.
, vol.45
, Issue.5
, pp. 1035-1044
-
-
Varano, F.1
Catarzi, D.2
Colotta, V.3
-
23
-
-
1842740287
-
3-Hydroxy-quinazoline-2,4-dione as a useful scaffold to obtain selective Gly/NMDA and AMPA receptor antagonists
-
COLOTTA V, CATARZI D, VARANO F et al.: 3-Hydroxy-quinazoline-2,4-dione as a useful scaffold to obtain selective Gly/NMDA and AMPA receptor antagonists. Bioorg. Med. Chem. Lett (2004) 14(9):2345-2349.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, Issue.9
, pp. 2345-2349
-
-
Colotta, V.1
Catarzi, D.2
Varano, F.3
-
24
-
-
17344388678
-
8-Methylureido-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e] pyrazines: Highly potent in vivo AMPA antagonists
-
MIGNANI S, BOHME GA, BOIREAU A et al.: 8-Methylureido-4, 5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e] pyrazines: highly potent in vivo AMPA antagonists. Bioorg. Med. Chem. Lett. (2000) 10(6):591-596.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, Issue.6
, pp. 591-596
-
-
Mignani, S.1
Bohme, G.A.2
Boireau, A.3
-
25
-
-
0034658574
-
4,10-Dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives: Highly potent and selective AMPA receptors antagonists with in vivo activity
-
STUTZMANN JM, BOHME GA, BOIREAU A et al.: 4,10-Dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives: highly potent and selective AMPA receptors antagonists with in vivo activity. Bioorg. Med. Chem. Lett. (2000) 10(10):1133-1137.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, Issue.10
, pp. 1133-1137
-
-
Stutzmann, J.M.1
Bohme, G.A.2
Boireau, A.3
-
26
-
-
0033859991
-
8-Methylureido-10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e] pyrazine-4-ones: Highly in vivo potent and selective AMPA receptor antagonists
-
JIMONET P, CHEVE M, BOHME GA et al.: 8-Methylureido- 10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-ones: highly in vivo potent and selective AMPA receptor antagonists. Bioorg. Med. Chem. (2000) 8(8):2211-2217.
-
(2000)
Bioorg. Med. Chem.
, vol.8
, Issue.8
, pp. 2211-2217
-
-
Jimonet, P.1
Cheve, M.2
Bohme, G.A.3
-
27
-
-
0034684750
-
Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2-a]indeno[1,2-e]pyrazin-8-and-9-carboxylic (acetic) acid AMPA antagonists
-
PRATT J, JIMONET P, BOHME GA et al.: Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2-a]indeno[1,2-e]pyrazin-8- and-9-carboxylic (acetic) acid AMPA antagonists. Bioorg. Med. Chem. Lett (2000) 10(24):2749-2754.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, Issue.24
, pp. 2749-2754
-
-
Pratt, J.1
Jimonet, P.2
Bohme, G.A.3
-
28
-
-
0035931586
-
Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin- 2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action
-
JIMONET P, BOHME GA, BOUQUEREL J et al.: Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin- 2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action. Bioorg. Med. Chem. Lett. (2001) 11(2):127-132.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.2
, pp. 127-132
-
-
Jimonet, P.1
Bohme, G.A.2
Bouquerel, J.3
-
29
-
-
0035821370
-
Synthesis of anticonvulsive AMPA antagonists: 4-oxo-10-substituted-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives
-
STUTZMANN JM, BOHME GA, BOIREAU A et al.: Synthesis of anticonvulsive AMPA antagonists: 4-oxo-10-substituted-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives. Bioorg. Med. Chem. Lett (2001) 11(9):1205-1210.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.9
, pp. 1205-1210
-
-
Stutzmann, J.M.1
Bohme, G.A.2
Boireau, A.3
-
30
-
-
18344378047
-
9-Carboxymethyl-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one-2- carboxyl ic acid (RPR-117824): Selective anticonvulsive and neuroprotective AMPA antagonist
-
MIGNANI S, BOHME GA, BIRRAUX G et al.: 9-Carboxymethyl-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one-2- carboxyl ic acid (RPR-117824): selective anticonvulsive and neuroprotective AMPA antagonist. Bioorg. Med. Chem. (2002) 10(5):1627-1637.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, Issue.5
, pp. 1627-1637
-
-
Mignani, S.1
Bohme, G.A.2
Birraux, G.3
-
31
-
-
0037362504
-
Structural requirements for novel willardiine derivatives acting as AMPA and kainate receptor antagonists
-
MORE JC, TROOP HM, DOLMAN NP, JANE DE: Structural requirements for novel willardiine derivatives acting as AMPA and kainate receptor antagonists. Br. J. Pharmacol. (2003) 138(6):1093-1100
-
(2003)
Br. J. Pharmacol.
, vol.138
, Issue.6
, pp. 1093-1100
-
-
More, J.C.1
Troop, H.M.2
Dolman, N.P.3
Jane, D.E.4
-
32
-
-
0032510841
-
2+ permeability and joro spider toxin sensitivity of AMPA and kainate receptors on cerebellar granule cells
-
2+ permeability and joro spider toxin sensitivity of AMPA and kainate receptors on cerebellar granule cells. Eur. J. Pharmacol. (1998) 351(1):131-138.
-
(1998)
Eur. J. Pharmacol.
, vol.351
, Issue.1
, pp. 131-138
-
-
Savidge, J.R.1
Bristow, D.R.2
-
33
-
-
0030814058
-
2+-Permeable AMPA receptors in cultured rat hippocampal neurons
-
2+-Permeable AMPA receptors in cultured rat hippocampal neurons. Neurosci. Res. (1997) 29(1):27-36.
-
(1997)
Neurosci. Res.
, vol.29
, Issue.1
, pp. 27-36
-
-
Koike, M.1
Iino, M.2
Ozawa, S.3
-
38
-
-
0027404879
-
GYKI 52466, a 2,3-benzodiazepine, is a highly selective, noncompetitive antagonist of AMPA/kainate receptor responses
-
DONEVAN SD, ROGAWSKI MA: GYKI 52466, a 2,3-benzodiazepine, is a highly selective, noncompetitive antagonist of AMPA/kainate receptor responses. Neuron (1993) 10(1):51-59.
-
(1993)
Neuron
, vol.10
, Issue.1
, pp. 51-59
-
-
Donevan, S.D.1
Rogawski, M.A.2
-
39
-
-
0027942174
-
Non-N-methyl-D-aspartate receptor antagonism by 3-N-substituted 2,3-benzodiazepines: Relationship to anticonvulsant activity
-
DONEVAN SD, YAMAGUCHI S, ROGAWSKI MA: Non-N-methyl-D-aspartate receptor antagonism by 3-N-substituted 2,3-benzodiazepines: relationship to anticonvulsant activity. J. Pharmacol. Exp. Ther (1994) 271(1):25-29.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.271
, Issue.1
, pp. 25-29
-
-
Donevan, S.D.1
Yamaguchi, S.2
Rogawski, M.A.3
-
40
-
-
0034782149
-
Talampanel. Antiepileptic, neuroprotectant, skeletal muscle relaxant
-
ANDRÁSI F: Talampanel. Antiepileptic, neuroprotectant, skeletal muscle relaxant. Drugs Fut. (2001) 26(8):754-756.
-
(2001)
Drugs Fut.
, vol.26
, Issue.8
, pp. 754-756
-
-
Andrási, F.1
-
41
-
-
0036751653
-
Negative allosteric modulation of AMPA-preferring receptors by the selective isomer GYKI 53784 (LY303070), a specific non-2 competitive AMPA antagonist
-
RUEL J, GUITTON MJ, PUELL JL: Negative allosteric modulation of AMPA-preferring receptors by the selective isomer GYKI 53784 (LY303070), a specific non-2 competitive AMPA antagonist. CNS Drug Rev. (2002) 8(3):235-254.
-
(2002)
CNS Drug Rev.
, vol.8
, Issue.3
, pp. 235-254
-
-
Ruel, J.1
Guitton, M.J.2
Puell, J.L.3
-
42
-
-
0034899184
-
Comparison of anticonvulsive and acute neuroprotective activity of three 2,3-benzodiazepine compounds, GM 52466, GYKI 53405, and GYKI 53655
-
SZABADOS T, GIGLER G, GACSALYI I, GYERTYAN I, LEVAY G: Comparison of anticonvulsive and acute neuroprotective activity of three 2,3-benzodiazepine compounds, GM 52466, GYKI 53405, and GYKI 53655. Brain Res. Bull. (2001) 55(3):387-391.
-
(2001)
Brain Res. Bull.
, vol.55
, Issue.3
, pp. 387-391
-
-
Szabados, T.1
Gigler, G.2
Gacsalyi, I.3
Gyertyan, I.4
Levay, G.5
-
43
-
-
0037108004
-
Protective effect of the antiepileptic drug candidate talampanel against AMPA-induced striatal neurotoxicity in neonatal rats
-
VILAGI I, TAKACS J, GULYAS-KOVACS A, BANCZEROWSKI-PELYHE I, TARNAWA I: Protective effect of the antiepileptic drug candidate talampanel against AMPA-induced striatal neurotoxicity in neonatal rats. Brain Res. Bull. (2002) 59(1):35-40.
-
(2002)
Brain Res. Bull.
, vol.59
, Issue.1
, pp. 35-40
-
-
Vilagi, I.1
Takacs, J.2
Gulyas-Kovacs, A.3
Banczerowski-Pelyhe, I.4
Tarnawa, I.5
-
44
-
-
0035935132
-
Solid-phase Friedel-Crafts acylation on polystyrene resins-synthesis of antiepiletic 1-aryl-3,5-dihydro-4H-2,3-benzodiazepin- 4-ones
-
BEVACQUA F, BASSO A, GITTO R, BRADLEY M, CHIMIRRI A: Solid-phase Friedel-Crafts acylation on polystyrene resins-synthesis of antiepiletic 1-aryl-3,5-dihydro-4H-2,3-benzodiazepin-4-ones. Tetrahedron Lett. (2001) 42(43):7683-7685.
-
(2001)
Tetrahedron Lett.
, vol.42
, Issue.43
, pp. 7683-7685
-
-
Bevacqua, F.1
Basso, A.2
Gitto, R.3
Bradley, M.4
Chimirri, A.5
-
45
-
-
0343527472
-
Structural analogues of some highly active non-competitive AMPA antagonists
-
HAMORI T, SOLYOM S, BERZSENYI P, ANDRASI F, TARNAWA I: Structural analogues of some highly active non-competitive AMPA antagonists. Bioorg. Med. Chem. Lett. (2000) 10(9):899-902.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, Issue.9
, pp. 899-902
-
-
Hamori, T.1
Solyom, S.2
Berzsenyi, P.3
Andrasi, F.4
Tarnawa, I.5
-
46
-
-
0036178207
-
Design and development of 2,3-benzodiazepine (CFM) noncompetitive AMPA receptor antagonists
-
GITTO R, ZAPPAL M, DE SG, CHIMIRRI A: Design and development of 2,3-benzodiazepine (CFM) noncompetitive AMPA receptor antagonists. Farmaco (2002) 57(2):129-134.
-
(2002)
Farmaco
, vol.57
, Issue.2
, pp. 129-134
-
-
Gitto, R.1
Zappal, M.2
De, S.G.3
Chimirri, A.4
-
47
-
-
0034787038
-
Research on new AMPA antagonists of 2,3-benzodiazepine type
-
SOLYOM S: Research on new AMPA antagonists of 2,3-benzodiazepine type. Pharmazie (2001) 56(Suppl.1)S62-66.
-
(2001)
Pharmazie
, vol.56
, Issue.SUPPL. 1
-
-
Solyom, S.1
-
48
-
-
0035952284
-
Synthesis and anticonvulsant activity of novel and potent 1-aryl-7,8-methylenedioxy-1,2,3,5-tetrahydro-4H-2,3-benzodiazepin- 4-one
-
GRASSO S, DE SARRO G, DE SARRO A et al.: Synthesis and anticonvulsant activity of novel and potent 1-aryl-7,8-methylenedioxy-1,2,3,5-tetrahydro-4H-2,3-benzodiazepin- 4-ones. Bioorg. Med. Chem. Lett (2001) 11(4):463-466.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.4
, pp. 463-466
-
-
Grasso, S.1
De Sarro, G.2
De Sarro, A.3
-
49
-
-
0037031608
-
Group III mGlu receptor agonists potentiate the anticonvulsant effect of AMPA and NMDA receptor block
-
DE SARRO G, CHIMIRRI A, MELDRUM BS: Group III mGlu receptor agonists potentiate the anticonvulsant effect of AMPA and NMDA receptor block. Eur. J. Pharmacol. (2002) 451(1):55-61.
-
(2002)
Eur. J. Pharmacol.
, vol.451
, Issue.1
, pp. 55-61
-
-
De Sarro, G.1
Chimirri, A.2
Meldrum, B.S.3
-
50
-
-
0343168061
-
New non competitive AMPA antagonists
-
ABRAHAM G, SOLYOM S, CSUZDI E et a;.: New non competitive AMPA antagonists. Bioorg. Med. Chem. (2000) 8(8):2127-2143.
-
(2000)
Bioorg. Med. Chem.
, vol.8
, Issue.8
, pp. 2127-2143
-
-
Abraham, G.1
Solyom, S.2
Csuzdi, E.3
-
51
-
-
0034649560
-
Synthesis and evaluation of pharmacological and pharmacokinetic properties of 11H-[1,2,4]triazolo[4,5-c][2,3]benzodiazepin-3(2H)-ones
-
ZAPPALA M, GITTO R, BEVACQUA F et al.: Synthesis and evaluation of pharmacological and pharmacokinetic properties of 11H-[1,2,4]triazolo[4,5-c][2,3]benzodiazepin-3(2H)-ones. J. Med. Chem. (2000) 43(25):4834-4839.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.25
, pp. 4834-4839
-
-
Zappala, M.1
Gitto, R.2
Bevacqua, F.3
-
52
-
-
0036753715
-
Synthesis and pharmacological properties of new 3-ethoxycarbonyl-11H-[1,2,4]triazolo[4,5-c][2,3]benzodiazepines
-
CHIMIRRI A, GITTO R, QUARTARONE S, ORLANDO V, DE SARRO A, DE SARRO GB: Synthesis and pharmacological properties of new 3-ethoxycarbonyl-11H-[1,2,4]triazolo[4,5-c][2,3]benzodiazepines. Farmaco (2002) 57(9):759-763.
-
(2002)
Farmaco
, vol.57
, Issue.9
, pp. 759-763
-
-
Chimirri, A.1
Gitto, R.2
Quartarone, S.3
Orlando, V.4
De Sarro, A.5
De Sarro, G.B.6
-
53
-
-
0042231981
-
Synthesis and evaluation of pharmacological properties of novel annelated 2,3-benzodiazepine derivatives
-
GITTO R, ORLANDO V, QUARTARONE S et al.: Synthesis and evaluation of pharmacological properties of novel annelated 2,3-benzodiazepine derivatives. J. Med. Chem. (2003) 46(17):3758-3761.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.17
, pp. 3758-3761
-
-
Gitto, R.1
Orlando, V.2
Quartarone, S.3
-
55
-
-
0033593926
-
Allosteric modulators of the AMPA receptor: Novel 6-substituted dihydrophthalazines
-
PEI XF, STURGESS MA, VALENZUELA CF, MACCECCHINI ML: Allosteric modulators of the AMPA receptor: novel 6-substituted dihydrophthalazines. Bioorg. Med. Chem. Lett. (1999) 9(4):539-542.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, Issue.4
, pp. 539-542
-
-
Pei, X.F.1
Sturgess, M.A.2
Valenzuela, C.F.3
Maccecchini, M.L.4
-
56
-
-
0030034762
-
Substituted 1,2-dihydrophthalazines: Potent, selective, and noncompetitive inhibitors of the AMPA receptor
-
PELLETIER JC, HESSON DP, JONES KA, COSTA AM: Substituted 1,2-dihydrophthalazines: potent, selective, and noncompetitive inhibitors of the AMPA receptor. J. Med. Chem. (1996) 39(2):343-346.
-
(1996)
J. Med. Chem.
, vol.39
, Issue.2
, pp. 343-346
-
-
Pelletier, J.C.1
Hesson, D.P.2
Jones, K.A.3
Costa, A.M.4
-
57
-
-
4344688172
-
Novel sulfur containing dihydrophthalazine antagonists of AMPA receptors
-
220th ACS Meeting. Washington DC, USA MEDI 212
-
LI BQ PEI XF, MACCECCHINI M: Novel sulfur containing dihydrophthalazine antagonists of AMPA receptors. 220th ACS Meeting. Washington DC, USA (2000) MEDI 212.
-
(2000)
-
-
Li, B.Q.1
Pei, X.F.2
Maccecchini, M.3
-
58
-
-
0033943607
-
Synthesis and pharmacological evaluation of 4-aryl-6,7-dimethoxyphthalazines as anticonvulsant agents
-
GITTO R, CHIMIRRI A, ZAPPALA M, DE SARRO G, DE SARRO, A. Synthesis and pharmacological evaluation of 4-aryl-6,7-dimethoxyphthalazines as anticonvulsant agents. Med. Chem. Res. (2000) 10(1):1-10.
-
(2000)
Med. Chem. Res.
, vol.10
, Issue.1
, pp. 1-10
-
-
Gitto, R.1
Chimirri, A.2
Zappala, M.3
De Sarro, G.4
De Sarro, A.5
-
59
-
-
0034721136
-
Synthesis and anticonvulsant activity of novel and potent 6,7-methylenedioxyphthalazin-1(2H)-ones
-
GRASSO S, DE SARRO G, DE SARRO A et al.: Synthesis and anticonvulsant activity of novel and potent 6,7-methylenedioxyphthalazin-1(2H)-ones. J. Med. Chem. (2000) 43 (15):2851-2859.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.15
, pp. 2851-2859
-
-
Grasso, S.1
De Sarro, G.2
De Sarro, A.3
-
60
-
-
0035942523
-
Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: Structure-activity relationship of the C-2 side chain tether
-
CHENARD BL, WELCH WM, BLAKE JF et al.: Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: structure-activity relationship of the C-2 side chain tether. J. Med. Chem. (2001) 44(11):1710-1717.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.11
, pp. 1710-1717
-
-
Chenard, B.L.1
Welch, W.M.2
Blake, J.F.3
-
61
-
-
0034608633
-
Methaqualone derivatives are potent noncompetitive AMPA receptor antagonists
-
CHENARD BL, MENNITI FS, PAGNOZZI MJ, SHENK KD, EWING FE, WELCH VIM: Methaqualone derivatives are potent noncompetitive AMPA receptor antagonists. Bioorg. Med. Chem. Lett. (2000) 10(11):1203-1205.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, Issue.11
, pp. 1203-1205
-
-
Chenard, B.L.1
Menniti, F.S.2
Pagnozzi, M.J.3
Shenk, K.D.4
Ewing, F.E.5
Welch, V.I.M.6
-
62
-
-
0037229785
-
CP-465,022, a selective noncompetitive AM PA receptor antagonist, blocks AMPA receptors but is not neuroprotective in vivo
-
MENNITI FS, BUCHAN AM, CHENARD BL et al.: CP-465,022, a selective noncompetitive AM PA receptor antagonist, blocks AMPA receptors but is not neuroprotective in vivo. Stroke (2003) 34(1):171-176.
-
(2003)
Stroke
, vol.34
, Issue.1
, pp. 171-176
-
-
Menniti, F.S.1
Buchan, A.M.2
Chenard, B.L.3
-
63
-
-
0036166553
-
Functional characterization of CP-465,022, a selective, noncompetitive AMPA receptor antagonist
-
LAZZARO JT, PATERNAIN AV, LERMA J et al.: Functional characterization of CP-465,022, a selective, noncompetitive AMPA receptor antagonist. Neuropharmacology (2002) 42(2):143-153.
-
(2002)
Neuropharmacology
, vol.42
, Issue.2
, pp. 143-153
-
-
Lazzaro, J.T.1
Paternain, A.V.2
Lerma, J.3
-
64
-
-
0035931552
-
Atropisomeric quinazolin-4-one derivatives are potent noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists
-
WELCH WM, EWING FE, HUANG J et al.: Atropisomeric quinazolin-4-one derivatives are potent noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists. Bioorg. Med Chem. Lett (2001) 11 (2):177-181.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, Issue.2
, pp. 177-181
-
-
Welch, W.M.1
Ewing, F.E.2
Huang, J.3
-
65
-
-
0033675261
-
Characterization of the binding site for a novel class of noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonists
-
MENNITI FS, CHENARD BL, COLLINS MB et al.: Characterization of the binding site for a novel class of noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonists. Mol. Pharmacol. (2000) 58(6):1310-1317.
-
(2000)
Mol. Pharmacol.
, vol.58
, Issue.6
, pp. 1310-1317
-
-
Menniti, F.S.1
Chenard, B.L.2
Collins, M.B.3
-
66
-
-
0038613421
-
Functional characterization of YM928, a novel moncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist
-
OHNO K, TSUTSUMI R, MATSUMOTO N et al.: Functional characterization of YM928, a novel moncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist. J. Pharmacol. Exp. Ther. (2003) 306 (1):66-72.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.306
, Issue.1
, pp. 66-72
-
-
Ohno, K.1
Tsutsumi, R.2
Matsumoto, N.3
-
67
-
-
9144262953
-
Effects of 2-[N-(4-chlorophenyl)-N-methylamino]-4H-pyrido[3.2-e]-1,3- thiazin-4-one (YM928), an orally active α -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonist, in models of generalized epileptic seizure in mice and rats
-
YAMASHITA H, OHNO K, AMADA Y et al.: Effects of 2-[N-(4-chlorophenyl)-N-methylamino]-4H-pyrido[3.2-e]-1,3- thiazin-4-one (YM928), an orally active α -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonist, in models of generalized epileptic seizure in mice and rats. J. Pharmacol. Exp. Ther. (2004) 308(1):127-133.
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.308
, Issue.1
, pp. 127-133
-
-
Yamashita, H.1
Ohno, K.2
Amada, Y.3
-
68
-
-
0036628390
-
Irampanel Boehringer Ingelheim
-
FEIGIN V: Irampanel Boehringer Ingelheim. Curr. Opin. Investig. Drugs (2002) 3(6):908-910.
-
(2002)
Curr. Opin. Investig. Drugs
, vol.3
, Issue.6
, pp. 908-910
-
-
Feigin, V.1
-
71
-
-
0037413584
-
Discovery of a novel and highly potent noncompetitive AMPA receptor antagonist
-
GITTO R, BARRECA ML, DE LUCA L et al.: Discovery of a novel and highly potent noncompetitive AMPA receptor antagonist. J. Med. Chem. (2003) 46(1):197-200.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.1
, pp. 197-200
-
-
Gitto, R.1
Barreca, M.L.2
De Luca, L.3
-
72
-
-
1642498133
-
Synthesis and anticonvulsant properties of tetrahydroisoquinoline derivatives
-
GITTO R, CARUSO R, ORLANDO V et al.: Synthesis and anticonvulsant properties of tetrahydroisoquinoline derivatives. Farmaco (2004) 59(1):7-12.
-
(2004)
Farmaco
, vol.59
, Issue.1
, pp. 7-12
-
-
Gitto, R.1
Caruso, R.2
Orlando, V.3
-
73
-
-
0347915541
-
Comparative anticonvulsant activity of N-acetyl-1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives in rodents
-
FERRERI G, CHIMIRRI A, RUSSO E et al.: Comparative anticonvulsant activity of N-acetyl-1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives in rodents. Pharmacol. Biochem. Behav. (2004) 77(1):85-94.
-
(2004)
Pharmacol. Biochem. Behav.
, vol.77
, Issue.1
, pp. 85-94
-
-
Ferreri, G.1
Chimirri, A.2
Russo, E.3
-
74
-
-
0037318781
-
Binding modes of noncompetitive AMPA antagonists: A computational approach
-
DE LUCA L, MACCHIARULO A, COSTANTINO G et al.: Binding modes of noncompetitive AMPA antagonists: a computational approach. Farmaco (2003) 58(2):107-113.
-
(2003)
Farmaco
, vol.58
, Issue.2
, pp. 107-113
-
-
De Luca, L.1
Macchiarulo, A.2
Costantino, G.3
-
75
-
-
0037365448
-
Pharmacophore modeling as an efficient tool in the discovery of novel noncompetitive AMPA receptor antagonists
-
BARRECA ML, GITTO R, QUARTARONE S, DE LUCA L, DE SARRO G, CHIMIRRI A. Pharmacophore modeling as an efficient tool in the discovery of novel noncompetitive AMPA receptor antagonists. J. Chem. Inf. Comput. Sci. (2003) 43(2):651-655.
-
(2003)
J. Chem. Inf. Comput. Sci.
, vol.43
, Issue.2
, pp. 651-655
-
-
Barreca, M.L.1
Gitto, R.2
Quartarone, S.3
De Luca, L.4
De Sarro, G.5
Chimirri, A.6
-
76
-
-
1642297214
-
QSAR study of anticonvulsant negative allosteric modulators of the AMPA receptor
-
MACCHIARULO A, DE LUCA L, COSTANTINO G et al.: QSAR study of anticonvulsant negative allosteric modulators of the AMPA receptor. J. Med. Chem. (2004) 47(7):1860-1863.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.7
, pp. 1860-1863
-
-
Macchiarulo, A.1
De Luca, L.2
Costantino, G.3
-
77
-
-
0033805231
-
Behavioural effects of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate-receptor antagonists and their relevance to substance abuse
-
JACKSON A, MEAD AN, STEPHENS DN: Behavioural effects of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate-receptor antagonists and their relevance to substance abuse. Pharmacol. Ther. (2000) 88(1):59-76.
-
(2000)
Pharmacol. Ther.
, vol.88
, Issue.1
, pp. 59-76
-
-
Jackson, A.1
Mead, A.N.2
Stephens, D.N.3
|