-
1
-
-
0026596478
-
Molecular neurobiology of glutamate receptors
-
Gasic, G. P.; Hollman, M. Molecular neurobiology of glutamate receptors. Annu. Rev. Physiol. 1992, 54, 507-536.
-
(1992)
Annu. Rev. Physiol.
, vol.54
, pp. 507-536
-
-
Gasic, G.P.1
Hollman, M.2
-
2
-
-
0028912822
-
The metabotropic glutamate receptors: Structure and functions
-
Pin, J.-P.; Duvosin, R. The metabotropic glutamate receptors: structure and functions. Neuropharmacology 1995, 34, 1-26.
-
(1995)
Neuropharmacology
, vol.34
, pp. 1-26
-
-
Pin, J.-P.1
Duvosin, R.2
-
3
-
-
0000583269
-
Agonists and antagonists for metabotropic glutamate receptors
-
Ornstein, P. L.; Monn, J. A.; Schoepp, D. D. Agonists and antagonists for metabotropic glutamate receptors. Curr. Pharm. Des. 1995, 1, 355-362.
-
(1995)
Curr. Pharm. Des.
, vol.1
, pp. 355-362
-
-
Ornstein, P.L.1
Monn, J.A.2
Schoepp, D.D.3
-
4
-
-
0025037594
-
Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate
-
Desai, M. A.; Conn, P. J. Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate. Neurosci. Lett. 1990, 109, 157-162. Palmer, E.; Monoghan, D. T.; Cotman, C. W. Trans-ACPD, a selective agonist to the PI-coupled excitatory amino acid receptor. Eur. J. Pharmacol. 1989, 166, 585-587.
-
(1990)
Neurosci. Lett.
, vol.109
, pp. 157-162
-
-
Desai, M.A.1
Conn, P.J.2
-
5
-
-
0024335555
-
Trans-ACPD, a selective agonist to the PI-coupled excitatory amino acid receptor
-
Desai, M. A.; Conn, P. J. Selective activation of phosphoinositide hydrolysis by a rigid analogue of glutamate. Neurosci. Lett. 1990, 109, 157-162. Palmer, E.; Monoghan, D. T.; Cotman, C. W. Trans-ACPD, a selective agonist to the PI-coupled excitatory amino acid receptor. Eur. J. Pharmacol. 1989, 166, 585-587.
-
(1989)
Eur. J. Pharmacol.
, vol.166
, pp. 585-587
-
-
Palmer, E.1
Monoghan, D.T.2
Cotman, C.W.3
-
6
-
-
0026756866
-
Agonist analysis of 2-(carboxycyclo- propyl)glycine isomers for cloned metabotropic glutamate receptor subtypes expressed in Chinese hamster ovary cells
-
Hayashi, Y.; Tanabe, Y.; Aramori, I.; Masu, M.; Shimamoto, K.; Ohfune, Y.; Nakanishi, S. Agonist analysis of 2-(carboxycyclo- propyl)glycine isomers for cloned metabotropic glutamate receptor subtypes expressed in Chinese hamster ovary cells. Br. J. Pharmacol. 1992, 107, 539-543.
-
(1992)
Br. J. Pharmacol.
, vol.107
, pp. 539-543
-
-
Hayashi, Y.1
Tanabe, Y.2
Aramori, I.3
Masu, M.4
Shimamoto, K.5
Ohfune, Y.6
Nakanishi, S.7
-
7
-
-
0027410488
-
Signal transduction, pharmacological properties, and expression patterns of two rat metabotropic glutamate receptors, mGluR3 and mGluR4
-
Tanabe, Y.; Nomura, A.; Masu, M.; Shigemoto, R.; Mizuno, N.; Nakanishi S. Signal transduction, pharmacological properties, and expression patterns of two rat metabotropic glutamate receptors, mGluR3 and mGluR4. J. Neurosci. 1993, 13, 1372-1378.
-
(1993)
J. Neurosci.
, vol.13
, pp. 1372-1378
-
-
Tanabe, Y.1
Nomura, A.2
Masu, M.3
Shigemoto, R.4
Mizuno, N.5
Nakanishi, S.6
-
8
-
-
0026614196
-
3,5-Dihydroxyphenylglycine: A potent agonist of metabotropic glutamate receptors
-
Ito, I.; Kohda, A.; Tanabe, S.; Hirose, E.; Hayashi, M.; Mitsunaga, S.; Sugiyama, H. 3,5-Dihydroxyphenylglycine: a potent agonist of metabotropic glutamate receptors. NeuroReport 1992, 3, 1013-1016. Schoepp, D. D.; Goldsworthy, J.; Johnson, B. G.; Salhoff, C. R.; Baker, S. R. J. Neurochem. 1994, 63, 769-772.
-
(1992)
NeuroReport
, vol.3
, pp. 1013-1016
-
-
Ito, I.1
Kohda, A.2
Tanabe, S.3
Hirose, E.4
Hayashi, M.5
Mitsunaga, S.6
Sugiyama, H.7
-
9
-
-
0027934857
-
-
Ito, I.; Kohda, A.; Tanabe, S.; Hirose, E.; Hayashi, M.; Mitsunaga, S.; Sugiyama, H. 3,5-Dihydroxyphenylglycine: a potent agonist of metabotropic glutamate receptors. NeuroReport 1992, 3, 1013-1016. Schoepp, D. D.; Goldsworthy, J.; Johnson, B. G.; Salhoff, C. R.; Baker, S. R. J. Neurochem. 1994, 63, 769-772.
-
(1994)
J. Neurochem.
, vol.63
, pp. 769-772
-
-
Schoepp, D.D.1
Goldsworthy, J.2
Johnson, B.G.3
Salhoff, C.R.4
Baker, S.R.5
-
10
-
-
8944234853
-
Synthesis of the four isomers of 4-aminopyrrolidine-2,4 dicarboxylate: Identification of a potent, highly selective, and systemically active agonist for metabotropic glutamate receptors negatively coupled to adenylate cyclase
-
Monn, J. A.; Valli, M. J.; Johnson, B. G.; Salhoff, C. R.; Wright, R. A.; Howe, T.; Bond, A.; Lodge, D.; Spangle, L. A.; Paschal, J. W.; Campbell, J. B.; Griffey, K.; Tizzano, J. P.; Schoepp, D. D. Synthesis of the four isomers of 4-aminopyrrolidine-2,4 dicarboxylate: Identification of a potent, highly selective, and systemically active agonist for metabotropic glutamate receptors negatively coupled to adenylate cyclase. J. Med. Chem. 1996, 39, 2990-3000.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2990-3000
-
-
Monn, J.A.1
Valli, M.J.2
Johnson, B.G.3
Salhoff, C.R.4
Wright, R.A.5
Howe, T.6
Bond, A.7
Lodge, D.8
Spangle, L.A.9
Paschal, J.W.10
Campbell, J.B.11
Griffey, K.12
Tizzano, J.P.13
Schoepp, D.D.14
-
11
-
-
15644369847
-
Design, synthesis and pharmacological characterization of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740): A potent, selective, and orally active group 2 metabotropic glutamate receptor antagonist possessing anticonvulsant and anxiolytic properties
-
Monn, J. A.; Valli, M. J.; Massey, S. M.; Wright, R. A.; Salhoff, C. R.; Johnson, B. G.; Howe, T.; Alt, C. A.; Rhodes, G. A.; Robey, R. L.; Griffey, K. R.; Tizzano, J. P.; Kallman, M. J.; Helton, D. R.; Schoepp, D. D. Design, synthesis and pharmacological characterization of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740): A potent, selective, and orally active group 2 metabotropic glutamate receptor antagonist possessing anticonvulsant and anxiolytic properties. J. Med. Chem. 1997, 40, 528-537.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 528-537
-
-
Monn, J.A.1
Valli, M.J.2
Massey, S.M.3
Wright, R.A.4
Salhoff, C.R.5
Johnson, B.G.6
Howe, T.7
Alt, C.A.8
Rhodes, G.A.9
Robey, R.L.10
Griffey, K.R.11
Tizzano, J.P.12
Kallman, M.J.13
Helton, D.R.14
Schoepp, D.D.15
-
12
-
-
0031055985
-
LY354740 Is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors
-
Schoepp, D. D. Johnson, B. G.; Wright, R. A.; Salhoff, C. R.; Mayne, N. G.; Wu, S.; Cockerham, S. L.; Burnett, J. P.; Belagaje, R.; Bleakman, D.; Monn, J. A. LY354740 Is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors. Neuropharmacology 1997, 36, 1-11.
-
(1997)
Neuropharmacology
, vol.36
, pp. 1-11
-
-
Schoepp, D.D.1
Johnson, B.G.2
Wright, R.A.3
Salhoff, C.R.4
Mayne, N.G.5
Wu, S.6
Cockerham, S.L.7
Burnett, J.P.8
Belagaje, R.9
Bleakman, D.10
Monn, J.A.11
-
13
-
-
0027209890
-
A novel metabotropic glutamate receptor agonist: Marked depression of monosynaptic excitation in newborn rat isolated spinal cord
-
Ishida, M.; Saitoh, T.; Shimamoto, K.; Ohfune, Y.; Shinozaki, H. A novel metabotropic glutamate receptor agonist: marked depression of monosynaptic excitation in newborn rat isolated spinal cord. Br. J. Pharmacol. 1993, 109, 1169-1177.
-
(1993)
Br. J. Pharmacol.
, vol.109
, pp. 1169-1177
-
-
Ishida, M.1
Saitoh, T.2
Shimamoto, K.3
Ohfune, Y.4
Shinozaki, H.5
-
14
-
-
0028169097
-
A novel metabotropic gluatamate receptor agonist: (2S,1′S, 2′R,3′R)-2-carboxy-3-methoxymethylcyclopropylglycine (cis-MCG.-I)
-
Ishida, M.; Saitoh, T.; Nakamura, Y.; Kataoka, K.; Shinozaki, H. A novel metabotropic gluatamate receptor agonist: (2S,1′S, 2′R,3′R)-2-carboxy-3-methoxymethylcyclopropyl)glycine (cis-MCG.-I). Eur. J. Pharmacol. [Mol. Pharmacol. Sect.] 1994, 268, 267-270.
-
(1994)
Eur. J. Pharmacol. [Mol. Pharmacol. Sect.]
, vol.268
, pp. 267-270
-
-
Ishida, M.1
Saitoh, T.2
Nakamura, Y.3
Kataoka, K.4
Shinozaki, H.5
-
15
-
-
0031055985
-
LY354740 is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors
-
Schoepp, D. D.; Johnson, B. G.; Wright, R. A.; Salhoff, C. R.; Mayne, N. G.; Wu. S.; Cockerham, S. L.; Burnett, J. P.; Belegaje, R.; Bleakman, D.; Monn, J. A. LY354740 is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors. Neuropharmacology 1997, 36, 1-11.
-
(1997)
Neuropharmacology
, vol.36
, pp. 1-11
-
-
Schoepp, D.D.1
Johnson, B.G.2
Wright, R.A.3
Salhoff, C.R.4
Mayne, N.G.5
Wu, S.6
Cockerham, S.L.7
Burnett, J.P.8
Belegaje, R.9
Bleakman, D.10
Monn, J.A.11
-
16
-
-
0025158065
-
Stereoselectivity and mode of inhibition of phosphoinositide- coupled excitatory amino acid receptors by 2-amino-3-phospho- nopropanoic acid
-
Schoepp, D. D.; Johnson, B. G.; Smith, E. C. R.; McQuaid, L. A. Stereoselectivity and mode of inhibition of phosphoinositide- coupled excitatory amino acid receptors by 2-amino-3-phospho- nopropanoic acid. Mol. Pharmacol. 1990, 38, 222-228.
-
(1990)
Mol. Pharmacol.
, vol.38
, pp. 222-228
-
-
Schoepp, D.D.1
Johnson, B.G.2
Smith, E.C.R.3
McQuaid, L.A.4
-
17
-
-
0028245013
-
Actions of two new antagonists showing selectivity for different subtypes of metabotropic glutamate receptor in the neonatal rat spinal cord
-
Jane, D. E.; Jones, P. L. St. J.; Pook, P. C.-K.; Tse, H.-W.; Watkins, J. C. Actions of two new antagonists showing selectivity for different subtypes of metabotropic glutamate receptor in the neonatal rat spinal cord. Br. J. Pharmacol. 1994, 112, 809-816.
-
(1994)
Br. J. Pharmacol.
, vol.112
, pp. 809-816
-
-
Jane, D.E.1
Jones, P.L.St.J.2
Pook, P.C.-K.3
Tse, H.-W.4
Watkins, J.C.5
-
18
-
-
0029871695
-
Stuctureactivity relationships of new agonists and antagonists of different metabotropic glutamate receptor subtypes
-
Sekiyama, N.; Hayashi, Y.; Nakanishi, S.; Jane, D. E.; Tse, H.- W.; Birse, E. F.; Watkins, J. C. Stuctureactivity relationships of new agonists and antagonists of different metabotropic glutamate receptor subtypes. Br. J. Pharmacol. 1996, 117, 1493-1503.
-
(1996)
Br. J. Pharmacol.
, vol.117
, pp. 1493-1503
-
-
Sekiyama, N.1
Hayashi, Y.2
Nakanishi, S.3
Jane, D.E.4
Tse, H.W.5
Birse, E.F.6
Watkins, J.C.7
-
19
-
-
0344799528
-
MGluRs negatively coupled to adenyl cyclase are potently antagonised by novel phosphono- and sulphono- but not tetrazolyl-substituted phenylglycine derivatives
-
Kemp, M. C.; Jane, D. E.; Tse, H.-W.; Roberts, P. J.; Watkins, J. C. mGluRs negatively coupled to adenyl cyclase are potently antagonised by novel phosphono- and sulphono- but not tetrazolyl-substituted phenylglycine derivatives. Br. J. Pharmacol. 1996, 116, 108P.
-
(1996)
Br. J. Pharmacol.
, vol.116
-
-
Kemp, M.C.1
Jane, D.E.2
Tse, H.-W.3
Roberts, P.J.4
Watkins, J.C.5
-
20
-
-
0029966777
-
The effects of (RS)-α-cyclopropyl-4-phosphonophenylglycine ((RS)-CPPG), a potent and selective metabotropic glutamate receptor antagonist
-
Toms, N. J.; Jane, D. E.; Kemp, M. C.; Bedingfield, J. S.; Roberts, P. J. The effects of (RS)-α-cyclopropyl-4-phosphonophenylglycine ((RS)-CPPG), a potent and selective metabotropic glutamate receptor antagonist. Br. J. Pharmacol. 1996, 119, 851-854.
-
(1996)
Br. J. Pharmacol.
, vol.119
, pp. 851-854
-
-
Toms, N.J.1
Jane, D.E.2
Kemp, M.C.3
Bedingfield, J.S.4
Roberts, P.J.5
-
21
-
-
0030026587
-
(2S,4S)-2-Amino-4-(4,4-diphenylbut-1-yl)pentane-1,5-dicarboxylic acid: A potent and selective antagonist for metabotrpic glutamate receptors negatively linked to adenylate cyclase
-
Wermuth, C. G.; Mann, A.; Schoenfelder, A.; Wright, R. A.; Johnson, B. G.; Burnett, J. P.; Mayne, N. G.; Schoepp, D. D. (2S,4S)-2-Amino-4-(4,4-diphenylbut-1-yl)pentane-1,5-dicarboxylic acid: a potent and selective antagonist for metabotrpic glutamate receptors negatively linked to adenylate cyclase. J. Med. Chem. 1996, 39, 814-816.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 814-816
-
-
Wermuth, C.G.1
Mann, A.2
Schoenfelder, A.3
Wright, R.A.4
Johnson, B.G.5
Burnett, J.P.6
Mayne, N.G.7
Schoepp, D.D.8
-
22
-
-
0029956082
-
Synthesis and pharmacological characterization of all sixteen stereoisomers of 2-(2′- carboxy-3′-phenylcyclopropyl)glycine. Focus on (2S,1′S,2′S,3′R)- 2-(2′-carboxy-3′-phenylcyclopropyl)glycine, a novel and selective group II metabotropic glutamate receptor antagonist
-
Pelliciari, R.; Marinozzi, M.; Natalini, B.; Costantino, G.; Luneia, R.; Giorgi, G.; Moroni, F.; Thomsen, C. Synthesis and pharmacological characterization of all sixteen stereoisomers of 2-(2′- carboxy-3′-phenylcyclopropyl)glycine. Focus on (2S,1′S,2′S,3′R)- 2-(2′-carboxy-3′-phenylcyclopropyl)glycine, a novel and selective group II metabotropic glutamate receptor antagonist. J. Med. Chem. 1996, 39, 2259-2269.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2259-2269
-
-
Pelliciari, R.1
Marinozzi, M.2
Natalini, B.3
Costantino, G.4
Luneia, R.5
Giorgi, G.6
Moroni, F.7
Thomsen, C.8
-
23
-
-
14444286701
-
2-Substituted (2SR)- 2-amino-2-(1SR,2SR)-2-carboxycycloprop-1-ylglycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2. Effects of aromatic substitution, pharmacological characterization, and bioavailability
-
Ornstein, P. L.; Bleisch, T. J.; Arnold, M. B.; Kennedy, J. H.; Wright, R. A.; Johnson, B. G.; Tizzano, J. P.; Helton, D. R.; Kallman, M. J.; Herin, M.; Schoepp, D. D. 2-Substituted (2SR)- 2-amino-2-(1SR,2SR)-2-carboxycycloprop-1-yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2. Effects of aromatic substitution, pharmacological characterization, and bioavailability. J. Med. Chem. 1998, 41, 358-378.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 358-378
-
-
Ornstein, P.L.1
Bleisch, T.J.2
Arnold, M.B.3
Kennedy, J.H.4
Wright, R.A.5
Johnson, B.G.6
Tizzano, J.P.7
Helton, D.R.8
Kallman, M.J.9
Herin, M.10
Schoepp, D.D.11
-
24
-
-
4243489506
-
Preparation and reactions of polyfunctional organozincate reagents in organic synthesis
-
Knochel, P.; Singer, R. D. Preparation and reactions of polyfunctional organozincate reagents in organic synthesis. Chem. Rev. 1993, 93, 2117-2188.
-
(1993)
Chem. Rev.
, vol.93
, pp. 2117-2188
-
-
Knochel, P.1
Singer, R.D.2
-
25
-
-
84948230696
-
A facile synthesis of phenylacetic acids from aryl ketones
-
Belletire, J. L.; Howard, H.; Donahue, K. A facile synthesis of phenylacetic acids from aryl ketones. Synth. Commun. 1982, 12, 763-770.
-
(1982)
Synth. Commun.
, vol.12
, pp. 763-770
-
-
Belletire, J.L.1
Howard, H.2
Donahue, K.3
-
26
-
-
15644378792
-
-
note
-
13C NMR of the hydantoin amino acids.
-
-
-
-
29
-
-
0029019890
-
Second-messenger responses in brain slices to elucidate novel glutamate receptors
-
Schoepp, D. D.; Johnson, B. G.; Salhoff, C. R.; Wright, R. A.; Goldsworthy, J. S.; Baker, S. R. Second-messenger responses in brain slices to elucidate novel glutamate receptors. J. Neurosci. Methods 1995, 59, 105-110.
-
(1995)
J. Neurosci. Methods
, vol.59
, pp. 105-110
-
-
Schoepp, D.D.1
Johnson, B.G.2
Salhoff, C.R.3
Wright, R.A.4
Goldsworthy, J.S.5
Baker, S.R.6
-
30
-
-
0028122371
-
Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase
-
Villalobos, A.; Blake, J. B.; Biggers, C. K.; Butler, T. W.; Chapin, D. S.; Chen, Y. L.; Ives, J. L.; Jones, S. B.; Liston, D. R.; Nagel, A. A.; Nason, D. M.; Nielsen, J. A.; Shalaby, I. A.; White, W. F. Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase. J. Med. Chem. 1994, 37, 2721-2734.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2721-2734
-
-
Villalobos, A.1
Blake, J.B.2
Biggers, C.K.3
Butler, T.W.4
Chapin, D.S.5
Chen, Y.L.6
Ives, J.L.7
Jones, S.B.8
Liston, D.R.9
Nagel, A.A.10
Nason, D.M.11
Nielsen, J.A.12
Shalaby, I.A.13
White, W.F.14
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