메뉴 건너뛰기




Volumn 47, Issue 2, 2004, Pages 456-466

(2S,1′S,2′R,3′R)-2-(2′-Carboxy-3′ -hydroxymethylcyclopropyl) Glycine Is a Highly Potent Group 2 and 3 Metabotropic Glutamate Receptor Agonist with Oral Activity

Author keywords

[No Author keywords available]

Indexed keywords

2 (2' CARBOXY 3' HYDROXYMETHYLCYCLOPROPYL)GLYCINE; GLYCINE DERIVATIVE; METABOTROPIC RECEPTOR AGONIST; UNCLASSIFIED DRUG; 2-(2'-CARBOXY-3'-HYDROXYMETHYLCYCLOPROPYL)GLYCINE; CYCLIC AMP; DRUG DERIVATIVE; GLYCINE; METABOTROPIC RECEPTOR; METABOTROPIC RECEPTOR 2; METABOTROPIC RECEPTOR 3;

EID: 0348223765     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm030967o     Document Type: Article
Times cited : (35)

References (83)
  • 2
    • 0027976271 scopus 로고
    • Excitatory Amino Acid Receptors: A Gallery of New Targets for Pharmocological Intervention
    • Cunningham, M. D.; Ferkany, J. W.; Enna, S. J. Excitatory Amino Acid Receptors: A Gallery Of New Targets For Pharmocological Intervention. Life Sci. 1994, 54, 135-148.
    • (1994) Life Sci. , vol.54 , pp. 135-148
    • Cunningham, M.D.1    Ferkany, J.W.2    Enna, S.J.3
  • 4
    • 0028340001 scopus 로고
    • Molecular Diversity and Functions of Glutamate Receptors
    • Nakanishi, S.; Masu, M. Molecular Diversity And Functions Of Glutamate Receptors. Annu. Rev. Biophys. Biomol. Struct. 1994, 23, 319-348.
    • (1994) Annu. Rev. Biophys. Biomol. Struct. , vol.23 , pp. 319-348
    • Nakanishi, S.1    Masu, M.2
  • 5
    • 0033118334 scopus 로고    scopus 로고
    • Molecular Tinkering of G protein-coupled Receptors: An Evolutionary Success
    • Bockaert, J.; Pin, J. P. Molecular Tinkering of G protein-coupled Receptors: an Evolutionary Success. EMBO J. 1999, 18, 1723-1729.
    • (1999) EMBO J. , vol.18 , pp. 1723-1729
    • Bockaert, J.1    Pin, J.P.2
  • 6
    • 0027992583 scopus 로고
    • Phenylglycine derivatives as antagonists of metabotropic glutamate receptors
    • For reviews see: (a) Watkins, J. C.; Collingridge, G. L. Phenylglycine derivatives as antagonists of metabotropic glutamate receptors. Trends Pharmacol. Sci. 1994, 15, 333-342.
    • (1994) Trends Pharmacol. Sci. , vol.15 , pp. 333-342
    • Watkins, J.C.1    Collingridge, G.L.2
  • 7
    • 0028912822 scopus 로고
    • The metabotropic glutamate receptors: Structure and functions
    • (b) Pin, J. P.; Duvoisin, R. The metabotropic glutamate receptors: structure and functions. Neuropharmacology 1995, 34, 1-26.
    • (1995) Neuropharmacology , vol.34 , pp. 1-26
    • Pin, J.P.1    Duvoisin, R.2
  • 8
    • 0029151828 scopus 로고
    • Pharmacological tools for the investigation of metabotropic glutamate receptors (mGluRs): Phenylglycine derivatives and other selective antagonists: Un update
    • (c) Roberts, P. J. Pharmacological tools for the investigation of metabotropic glutamate receptors (mGluRs): phenylglycine derivatives and other selective antagonists: un update. Neuropharmacology 1995, 34, 813-819.
    • (1995) Neuropharmacology , vol.34 , pp. 813-819
    • Roberts, P.J.1
  • 9
    • 0030995878 scopus 로고    scopus 로고
    • Pharmacology and functions of metabotropic glutamate receptors
    • (d) Conn, P. J.; Pin, P. J. Pharmacology and functions of metabotropic glutamate receptors. Annu. Rev. Pharmacol. Toxicol. 1997, 37, 205-237.
    • (1997) Annu. Rev. Pharmacol. Toxicol. , vol.37 , pp. 205-237
    • Conn, P.J.1    Pin, P.J.2
  • 10
    • 0033057319 scopus 로고    scopus 로고
    • New perspectives for the development of selective metabotropic glutamate receptor ligands
    • (e) Pin, J. P.; De Colle, C.; Bessis, A. S.; Acher, F. New perspectives for the development of selective metabotropic glutamate receptor ligands. Eur. J. Pharmacol. 1999, 375, 277-294.
    • (1999) Eur. J. Pharmacol. , vol.375 , pp. 277-294
    • Pin, J.P.1    De Colle, C.2    Bessis, A.S.3    Acher, F.4
  • 11
    • 0032834028 scopus 로고    scopus 로고
    • Pharmacological agents acting at subtypes of metabotropic glutamate receptors
    • (f) Schoepp, D. D.; Jane, D. E.; Monn, J. A. Pharmacological agents acting at subtypes of metabotropic glutamate receptors. Neuropharmacology 1999, 38, 1431-1476.
    • (1999) Neuropharmacology , vol.38 , pp. 1431-1476
    • Schoepp, D.D.1    Jane, D.E.2    Monn, J.A.3
  • 12
    • 0025079146 scopus 로고
    • (2S,3S,4S)-α-(Carboxycyclopropyl) glycine is a novel agonist of metabotropic glutamate receptors
    • Nakagawa, Y.; Saitoh, K.; Ishihara, T.; Ishida, M.; Shinozaki, H. (2S,3S,4S)-α-(Carboxycyclopropyl) glycine is a novel agonist of metabotropic glutamate receptors. Eur. J. Pharmacol. 1990, 184, 205-206.
    • (1990) Eur. J. Pharmacol. , vol.184 , pp. 205-206
    • Nakagawa, Y.1    Saitoh, K.2    Ishihara, T.3    Ishida, M.4    Shinozaki, H.5
  • 13
    • 0026756866 scopus 로고
    • Agonist analysis of 2-(carboxycyclopropyl) 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-(carboxycyclopropyl) 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
  • 14
    • 0032483142 scopus 로고    scopus 로고
    • Peparation of difluoro analogues of CCGs and their pharmacological evaluations
    • Shibuya, A.; Sato, A.; Taguchi, T. Peparation of difluoro analogues of CCGs and their pharmacological evaluations. Bioorg. Med. Chem. Lett. 1998, 8, 1979-1984.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 1979-1984
    • Shibuya, A.1    Sato, A.2    Taguchi, T.3
  • 15
    • 85064549206 scopus 로고
    • Inversion of cis-substituted α-cyclopropyl acyl anion. Stereoselective entry to the synthesis of a potent metabotropic glutamate agonist, (2S,1′S,2′S)-2-(carboxycyclopropyl) glycine (L-CCG-I), and its 3′-substituted analogues
    • Shimamoto, K.; Ohfune, Y. Inversion of cis-substituted α-cyclopropyl acyl anion. Stereoselective entry to the synthesis of a potent metabotropic glutamate agonist, (2S,1′S,2′ S)-2-(carboxycyclopropyl) glycine (L-CCG-I), and its 3′-substituted analogues. SynLett 1993, 919-920.
    • (1993) SynLett , pp. 919-920
    • Shimamoto, K.1    Ohfune, Y.2
  • 16
    • 0031713304 scopus 로고    scopus 로고
    • Comparative effect of L-CCG-I, DCG-IV and γ-carboxy-L-glutamate on all cloned metabotropic glutamate receptor subtypes
    • Brabet, I.; Parmentier, M. L.; De Colle, C.; Bockaert, J.; Acher, F.; Pin, J. P. Comparative effect of L-CCG-I, DCG-IV and γ -carboxy-L-glutamate on all cloned metabotropic glutamate receptor subtypes. Neuropharmacology 1998, 37, 1043-1051.
    • (1998) Neuropharmacology , vol.37 , pp. 1043-1051
    • Brabet, I.1    Parmentier, M.L.2    De Colle, C.3    Bockaert, J.4    Acher, F.5    Pin, J.P.6
  • 18
    • 0037101811 scopus 로고    scopus 로고
    • (2S,1′S,2′S,3′R)-2-(2′-Carboxy-3′ -methylcyclopropyl) glycine is a potent and selective Metabotropic Group 2 Receptor Agonists with Anxiolytic Properties
    • Collado, I.; Pedregal, C.; Mazón, A.; Espinosa, J. F.; Blanco-Urgoiti, J.; Schoepp, D.; Wright, R. A.; Johnson, B.; Kingston, A. (2S,1′S,2′S,3′R)-2-(2′-Carboxy-3′ -methylcyclopropyl) glycine is a potent and selective Metabotropic Group 2 Receptor Agonists with Anxiolytic Properties. J. Med. Chem. 2002, 45, 3619-3629.
    • (2002) J. Med. Chem. , vol.45 , pp. 3619-3629
    • Collado, I.1    Pedregal, C.2    Mazón, A.3    Espinosa, J.F.4    Blanco-Urgoiti, J.5    Schoepp, D.6    Wright, R.A.7    Johnson, B.8    Kingston, A.9
  • 19
    • 0029956082 scopus 로고    scopus 로고
    • Synthesis and Pharmacological Characterization of All Sixteen Stereoisomers of 2-(2′-Carboxy-3′-phenylcyclopropyl)glycine. Focuson(2S,1′S,2′S,3′R)-2-(2′-Carboxy-3′ -phenylcyclopropyl) glycine, a Novel and Selective Group II Metabotropic Glutamate Receptors Antagonist
    • (a) Pellicciari, 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. Focuson(2S,1′S,2′S,3′ R)-2-(2′-Carboxy-3′-phenylcyclopropyl) glycine, a Novel and Selective Group II Metabotropic Glutamate Receptors Antagonist. J. Med. Chem. 1996, 39, 2259-2269.
    • (1996) J. Med. Chem. , vol.39 , pp. 2259-2269
    • Pellicciari, R.1    Marinozzi, M.2    Natalini, B.3    Costantino, G.4    Luneia, R.5    Giorgi, G.6    Moroni, F.7    Thomsen, C.8
  • 20
    • 0030591706 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Enantiomerically Pure (2S,1′S,2′ S,3′R)-Phenylcarboxycyclopropylglycine (PCCG-4): A Potent and Selective Ligand at Group II Metabotropic Glutamate Receptors
    • (b) Marinozzi, M.; Natalini, B.; Constantino, G.; Tijskens, P.; Thomsen, C.; Pellicciari, R. Asymmetric Synthesis of Enantiomerically Pure (2S,1′S,2′S,3′R)-Phenylcarboxycyclopropylglycine (PCCG-4): A Potent and Selective Ligand at Group II Metabotropic Glutamate Receptors. Bioorg. Med. Chem. Lett. 1996, 6, 2243-2246.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 2243-2246
    • Marinozzi, M.1    Natalini, B.2    Constantino, G.3    Tijskens, P.4    Thomsen, C.5    Pellicciari, R.6
  • 21
    • 0035904868 scopus 로고    scopus 로고
    • Design, Synthesis and Preliminary Evaluation of Novel 3′-Substituted Carboxycyclopropylglycines as Antagonists at Group 2 Metabotropic Glutamate Receptors
    • Pellicciari, R.; Costantino, G.; Marinozzi, M.; Macchiarulo, A.; Amori, L.; Flor, P. J.; Gasparini, F.; Kuhn, R.; Urwyler, S. Design, Synthesis and Preliminary Evaluation of Novel 3′-Substituted Carboxycyclopropylglycines as Antagonists at Group 2 Metabotropic Glutamate Receptors. Bioorg. Med. Chem. Lett. 2001, 11, 3179-3182.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 3179-3182
    • Pellicciari, R.1    Costantino, G.2    Marinozzi, M.3    Macchiarulo, A.4    Amori, L.5    Flor, P.J.6    Gasparini, F.7    Kuhn, R.8    Urwyler, S.9
  • 22
    • 0032576734 scopus 로고    scopus 로고
    • 2-Substituted ((1SR,2SR)-2-Carboxycycloprop-1-yl) glycines as Potent and Selective antagonist of group II metabotropic receptors. 1. Effects of alkyl, arylalkyl, and diarylalkyl substitution
    • Ornstein, P. L.; Bleisch, T. J.; Arnold, M. B.; Wright, R. A.; Johnson, B. G.; Schoepp, D. D. 2-Substituted ((1SR,2SR)-2-Carboxycycloprop-1-yl) glycines as Potent and Selective antagonist of group II metabotropic receptors. 1. Effects of alkyl, arylalkyl, and diarylalkyl substitution. J. Med. Chem. 1998, 41, 346-357.
    • (1998) J. Med. Chem. , vol.41 , pp. 346-357
    • Ornstein, P.L.1    Bleisch, T.J.2    Arnold, M.B.3    Wright, R.A.4    Johnson, B.G.5    Schoepp, D.D.6
  • 25
    • 0000182438 scopus 로고
    • Stereochemistry of the Bucherer-Bergs and Strecker Reactions of 4-tert-Butylcyclohexanone
    • Edward, J. T.; Jitrangsri, C. Stereochemistry of the Bucherer-Bergs and Strecker Reactions of 4-tert-Butylcyclohexanone. Can. J. Chem. 1975, 53, 3339-3350.
    • (1975) Can. J. Chem. , vol.53 , pp. 3339-3350
    • Edward, J.T.1    Jitrangsri, C.2
  • 26
    • 0037449352 scopus 로고    scopus 로고
    • Synthesis and Structure-Activity Relationship Studies of Novel 2-Diarylethyl Substituted (2-Carboxycycloprop-1-yl) Glycines as High-Affinity Group II Metabotropic Glutamate Receptor Ligands
    • Sorensen, U. S.; Bleisch, T. J.; Kingston, A. E.; Wright, R. A.; Johnson, B. G.; Schoepp, D. D.; Ornstein, P. L. Synthesis and Structure-Activity Relationship Studies of Novel 2-Diarylethyl Substituted (2-Carboxycycloprop-1-yl) Glycines as High-Affinity Group II Metabotropic Glutamate Receptor Ligands. Bioorg. Med. Chem. 2003, 11, 197-205.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 197-205
    • Sorensen, U.S.1    Bleisch, T.J.2    Kingston, A.E.3    Wright, R.A.4    Johnson, B.G.5    Schoepp, D.D.6    Ornstein, P.L.7
  • 28
    • 0029164640 scopus 로고
    • Enantioselective catalytic intramolecular cyclopropanation of allylic α-diazopropionates optimized with dirhodium(II) tetrakis[methyl 2-oxazolidinone-4(S or R)-carboxylate]
    • (b) Doyle, M. P.; Zhou, Q.-L. Enantioselective catalytic intramolecular cyclopropanation of allylic α-diazopropionates optimized with dirhodium(II) tetrakis[methyl 2-oxazolidinone-4(S or R)-carboxylate]. Tetrahedron: Asymmetry 1995, 6, 2157-2160.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 2157-2160
    • Doyle, M.P.1    Zhou, Q.-L.2
  • 29
    • 0028889537 scopus 로고
    • Enhancement of enantiocontrol/diastereocontrol in catalytic intramolecular cyclopropanation and carbon-hydrogen insertion reactions of diazoacetates with Rh2-(4S-MPPIM)4
    • (c) Doyle, M. P.; Dyatkin, A. B.; Ruppar, D. A. Enhancement of enantiocontrol/diastereocontrol in catalytic intramolecular cyclopropanation and carbon-hydrogen insertion reactions of diazoacetates with Rh2-(4S-MPPIM)4. Tetrahedron Lett. 1995, 36, 7579-7582.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7579-7582
    • Doyle, M.P.1    Dyatkin, A.B.2    Ruppar, D.A.3
  • 30
    • 0026471806 scopus 로고
    • Enantioselective, rhodium catalyzed intramolecular cyclopropanations of homoallylic diazoacetates
    • (d) Martin, S. M.; Oalmann, C. J.; Liras, S. Enantioselective, rhodium catalyzed intramolecular cyclopropanations of homoallylic diazoacetates. Tetrahedron Lett. 1992, 33, 6727-6730.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6727-6730
    • Martin, S.M.1    Oalmann, C.J.2    Liras, S.3
  • 31
    • 1542500184 scopus 로고    scopus 로고
    • Comparative evaluation of enantiocontrol for intramolecular cyclopropanation ofdiazoacetates with chiral CuI, RhII and RuII catalysts
    • Doyle, M. P.; Peterson, C. S.; Zhou, Q.-L.; Nishiyama, H. Comparative evaluation of enantiocontrol for intramolecular cyclopropanation ofdiazoacetates with chiral CuI, RhII and RuII catalysts. Chem. Commun. 1997, 211-212.
    • (1997) Chem. Commun. , pp. 211-212
    • Doyle, M.P.1    Peterson, C.S.2    Zhou, Q.-L.3    Nishiyama, H.4
  • 32
    • 0347940393 scopus 로고    scopus 로고
    • note
    • 6 of the corresponding monoacetate obtained by reaction of 19 with methyllithium and subsequent acetylation.21a
  • 33
    • 0029164282 scopus 로고
    • α-Phenylglycinol as chiral auxiliary in diastereoselective Strecker synthesis of α-amino acids
    • Chakraborty, T. K.; Azhar Hussain, K.; Venkat Reddy, G. α-Phenylglycinol as chiral auxiliary in diastereoselective Strecker synthesis of α-amino acids. Tetrahedron 1995, 51, 9179.
    • (1995) Tetrahedron , vol.51 , pp. 9179
    • Chakraborty, T.K.1    Azhar Hussain, K.2    Venkat Reddy, G.3
  • 34
    • 0029113130 scopus 로고
    • Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2R,4R-4-amino-pyrrolidine-2,4-dicarboxylate
    • Schoepp, D. D.; Johnson, B. G.; Salhoff, C. R.; Valli, M. J.; Desai, M. A.; Burnett, J. P.; Mayne, N. G.; Monn, J. A. Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2R,4R-4-amino-pyrrolidine-2,4-dicarboxylate. Neuropharmacology 1995, 34, 843-850.
    • (1995) Neuropharmacology , vol.34 , pp. 843-850
    • Schoepp, D.D.1    Johnson, B.G.2    Salhoff, C.R.3    Valli, M.J.4    Desai, M.A.5    Burnett, J.P.6    Mayne, N.G.7    Monn, J.A.8
  • 35
    • 0025827941 scopus 로고
    • In vitro and in vivo pharmacology of trans- and cis-(± )-1-amino-1,3-cyclopentanedicarboxylic acid: Dissociation of metabotropic and ionotropic excitatory amino acid receptor effects
    • Schoepp, D. D.; Johnson, B. G.; Salhoff, C. R.; McDonald, J. W.; Johnston, M. V. In vitro and in vivo pharmacology of trans- and cis-(±)-1-amino-1,3-cyclopentanedicarboxylic acid: dissociation of metabotropic and ionotropic excitatory amino acid receptor effects. J. Neurochem. 1991, 56, 1789-1796.
    • (1991) J. Neurochem. , vol.56 , pp. 1789-1796
    • Schoepp, D.D.1    Johnson, B.G.2    Salhoff, C.R.3    McDonald, J.W.4    Johnston, M.V.5
  • 36
    • 0028933301 scopus 로고
    • Molecular cloning, functional expression and pharmacological characterization of the human metabotropic glutamate receptor type 2
    • (a) Flor, P. J.; Lindauer, K.; Puttner, I.; Ruegg, D.; Lukic, S.; Knöfel, R.; Kuhn, R. Molecular cloning, functional expression and pharmacological characterization of the human metabotropic glutamate receptor type 2. Eur. J. Neurosci. 1995, 7, 622-629.
    • (1995) Eur. J. Neurosci. , vol.7 , pp. 622-629
    • Flor, P.J.1    Lindauer, K.2    Puttner, I.3    Ruegg, D.4    Lukic, S.5    Knöfel, R.6    Kuhn, R.7
  • 37
    • 0033980570 scopus 로고    scopus 로고
    • Distinct influence of the group III metabotropic glutamate receptor agonist (R,S)-4-phosphonophenylglycine on different forms of neuronal damage
    • (b) Flor, P. J.; Henrich-Noack, P.; Sabelhaus, C. F.; Prass, K.; Dirnagl, U.; Gasparini, F.; Sauter, A.; Rudin, M.; Reymann, K. G. Distinct influence of the group III metabotropic glutamate receptor agonist (R,S)-4-phosphonophenylglycine on different forms of neuronal damage. Neuropharmacology 2000, 39, 911-917.
    • (2000) Neuropharmacology , vol.39 , pp. 911-917
    • Flor, P.J.1    Henrich-Noack, P.2    Sabelhaus, C.F.3    Prass, K.4    Dirnagl, U.5    Gasparini, F.6    Sauter, A.7    Rudin, M.8    Reymann, K.G.9
  • 38
    • 0035136627 scopus 로고    scopus 로고
    • (S)-3,4-DCPG, a potent and selective mGlu8a receptor agonist, activates metabotropic glutamate receptors on primary afferent terminals in the neonatal rat spinal cord
    • (c) Thomas, N. K.; Wright, R. A.; Howson, P. A.; Kingston, A. E.; Schoepp, D. D.; Jane, D. E. (S)-3,4-DCPG, a potent and selective mGlu8a receptor agonist, activates metabotropic glutamate receptors on primary afferent terminals in the neonatal rat spinal cord. Neuropharmacology 2001, 40, 311-318.
    • (2001) Neuropharmacology , vol.40 , pp. 311-318
    • Thomas, N.K.1    Wright, R.A.2    Howson, P.A.3    Kingston, A.E.4    Schoepp, D.D.5    Jane, D.E.6
  • 39
    • 0032575715 scopus 로고    scopus 로고
    • Reversal of Phencyclidine Effects by a Group II Metabotropic Glutamate Receptor Agonist in Rats
    • (a) Moghaddam, B.; Adams, B. W. Reversal of Phencyclidine Effects by a Group II Metabotropic Glutamate Receptor Agonist in Rats. Science 1998, 281, 1349-1352.
    • (1998) Science , vol.281 , pp. 1349-1352
    • Moghaddam, B.1    Adams, B.W.2
  • 40
    • 0032785165 scopus 로고    scopus 로고
    • Serotonin-Glutamate Interactions: A New Target for Antipsychotic Drugs
    • (b) Aghajanian, G. K.; Marek, G. J. Serotonin-Glutamate Interactions: A New Target for Antipsychotic Drugs. Neuropsychopharmacology 1999, 21 (S6), S122-S133.
    • (1999) Neuropsychopharmacology , vol.21 , Issue.S6
    • Aghajanian, G.K.1    Marek, G.J.2
  • 41
    • 0032848507 scopus 로고    scopus 로고
    • The Metabotropic Glutamate 2/3 Receptor Agonists LY354740 and LY379268 Selectively Attenuate Phencyclidine versus d-Amphetamine Motor Behavours in Rats
    • (c) Cartmell, J.; Monn, J. A.; Darryle, D. D. The Metabotropic Glutamate 2/3 Receptor Agonists LY354740 and LY379268 Selectively Attenuate Phencyclidine versus d-Amphetamine Motor Behavours in Rats. J. Pharmacol. Exp. Ther. 1999, 291, 161-170.
    • (1999) J. Pharmacol. Exp. Ther. , vol.291 , pp. 161-170
    • Cartmell, J.1    Monn, J.A.2    Darryle, D.D.3
  • 42
    • 0034068655 scopus 로고    scopus 로고
    • Attenuation of specific PCP-evoked behaviors by the potent mGlu2/3 receptor agonist, LY379268 and comparison with the atypical antipsychotic, clozapine
    • (d) Cartmell, J.; Monn, J. A.; Darryle, D. D. Attenuation of specific PCP-evoked behaviors by the potent mGlu2/3 receptor agonist, LY379268 and comparison with the atypical antipsychotic, clozapine. Psychopharmacology 2000, 148, 423-439.
    • (2000) Psychopharmacology , vol.148 , pp. 423-439
    • Cartmell, J.1    Monn, J.A.2    Darryle, D.D.3
  • 43
    • 0033959387 scopus 로고    scopus 로고
    • LY354740 Affects Startle Responding but not Sensorimotor Gating or Discriminative Effects of Phencyclidine
    • (e) Schreiber, R.; Lowe, D.; Voerste, A.; De Vry, J. LY354740 Affects Startle Responding but not Sensorimotor Gating or Discriminative Effects of Phencyclidine. Eur. J. Pharmacol. 2000, 388, R3-R4.
    • (2000) Eur. J. Pharmacol. , vol.388
    • Schreiber, R.1    Lowe, D.2    Voerste, A.3    De Vry, J.4
  • 44
    • 0034698431 scopus 로고    scopus 로고
    • The mGlu2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing
    • (f) Cartmell, J.; Monn, J. A.; Schoepp, D. D. The mGlu2/3 receptor agonist LY379268 selectively blocks amphetamine ambulations and rearing. Eur. J. Pharmacol. 2000, 400, 221-224.
    • (2000) Eur. J. Pharmacol. , vol.400 , pp. 221-224
    • Cartmell, J.1    Monn, J.A.2    Schoepp, D.D.3
  • 45
    • 0033844761 scopus 로고    scopus 로고
    • The Potent, Selective mGlu2/3 Receptor Agonist LY379268 Increases Extracellular Levels of Dopamine, 3,4-Dihydroxyphenylacetic Acid, Homovanillic Acid and 5-Hydroxyindole-3-Acetic Acid in the Medial Prefrontal Cortex of the Freely Moving Rat
    • (g) Cartmell, J.; Kenneth, W. P.; Salhoff, R. C.; Monn, J. A.; Schoepp, D. D. The Potent, Selective mGlu2/3 Receptor Agonist LY379268 Increases Extracellular Levels of Dopamine, 3,4-Dihydroxyphenylacetic Acid, Homovanillic Acid and 5-Hydroxyindole-3-Acetic Acid in the Medial Prefrontal Cortex of the Freely Moving Rat. J. Neurochem. 2000, 75, 1147-1154.
    • (2000) J. Neurochem. , vol.75 , pp. 1147-1154
    • Cartmell, J.1    Kenneth, W.P.2    Salhoff, R.C.3    Monn, J.A.4    Schoepp, D.D.5
  • 46
    • 0011900802 scopus 로고    scopus 로고
    • Preclinical Pharmacology of mGlu2/3 Receptor Agonists: Novel Agents for Schizophrenia?
    • (h) Schoepp, D. D.; Maker, G. J. Preclinical Pharmacology of mGlu2/3 Receptor Agonists: Novel Agents for Schizophrenia? Curr. Drug Targets 2002, 1, 215-225.
    • (2002) Curr. Drug Targets , vol.1 , pp. 215-225
    • Schoepp, D.D.1    Maker, G.J.2
  • 48
    • 0031933951 scopus 로고    scopus 로고
    • Anxiolytic and side-effects profile of LY354740: A potent, highly selective, orrally active agonist for group II metabotropic glutamate receptors
    • (a) Helton, D. R.; Tizzano, J. P.; Monn, J. A.; Schoepp, D. D.; Kallman, M. J. Anxiolytic and side-effects profile of LY354740: A potent, highly selective, orrally active agonist for group II metabotropic glutamate receptors. J. Pharmacol. Exp. Ther. 1998, 284, 651-660.
    • (1998) J. Pharmacol. Exp. Ther. , vol.284 , pp. 651-660
    • Helton, D.R.1    Tizzano, J.P.2    Monn, J.A.3    Schoepp, D.D.4    Kallman, M.J.5
  • 49
    • 0344980107 scopus 로고    scopus 로고
    • Potential anti-anxiety, anti-additive effects of LY354740, a selective group 2 glutamate metabotropic receptors agonist in animal models
    • (b) Klodzinska, A.; Chojnacka-Wojcik, E.; Palucha, A.; Branski, P.; Popik, P.; Pilc, A. Potential anti-anxiety, anti-additive effects of LY354740, a selective group 2 glutamate metabotropic receptors agonist in animal models. Neuropharmacology 1999, 38, 1831-1839.
    • (1999) Neuropharmacology , vol.38 , pp. 1831-1839
    • Klodzinska, A.1    Chojnacka-Wojcik, E.2    Palucha, A.3    Branski, P.4    Popik, P.5    Pilc, A.6
  • 50
    • 0033050341 scopus 로고    scopus 로고
    • Disinhibitory Effects of LY354740, a New mGluR2 Agonist, on Behaviors Suppressed by Electric Shock in Rats and Pigeons
    • (c) Benvenga, M. J.; Overshiner, C. D.; Monn, J. A.; Leander, J. D. Disinhibitory Effects of LY354740, a New mGluR2 Agonist, on Behaviors Suppressed by Electric Shock in Rats and Pigeons. Drug Dev. Res. 1999, 47, 37-44.
    • (1999) Drug Dev. Res. , vol.47 , pp. 37-44
    • Benvenga, M.J.1    Overshiner, C.D.2    Monn, J.A.3    Leander, J.D.4
  • 51
    • 0034100686 scopus 로고    scopus 로고
    • LY354740, a potent group II metabotropic glutamate receptor agonist prevents lactate-induced panic-like response in panic-prone rats
    • (d) Shekhar, A.; Keim, S. R. LY354740, a potent group II metabotropic glutamate receptor agonist prevents lactate-induced panic-like response in panic-prone rats. Neuropharmacology 2000, 39, 1139-1146.
    • (2000) Neuropharmacology , vol.39 , pp. 1139-1146
    • Shekhar, A.1    Keim, S.R.2
  • 52
    • 0033800774 scopus 로고    scopus 로고
    • Stimulation of group II metabotropic glutamate receptor or inhibition of group I ones exerts anxiolytic-like effects in rats
    • (e) Pilc, A.; Chojnacka-Wójcik, E.; Tatarczynska, E.; Borycz, J.; Kroczka, B. Stimulation of group II metabotropic glutamate receptor or inhibition of group I ones exerts anxiolytic-like effects in rats. Amino Acids 2000, 19, 81-86.
    • (2000) Amino Acids , vol.19 , pp. 81-86
    • Pilc, A.1    Chojnacka-Wójcik, E.2    Tatarczynska, E.3    Borycz, J.4    Kroczka, B.5
  • 53
    • 0035996365 scopus 로고    scopus 로고
    • The anxiolytic action of mGlu2/3 receptor agonist, LY354740, in the fear-potentiated startle in rats is mechanistically distinct from diazepam
    • (f) Tizzano, P. J.; Griffey, K. I.; Schoepp, D. D. The anxiolytic action of mGlu2/3 receptor agonist, LY354740, in the fear-potentiated startle in rats is mechanistically distinct from diazepam. Pharmacol., Biochem. Behav. 2002, 73, 367-374.
    • (2002) Pharmacol., Biochem. Behav. , vol.73 , pp. 367-374
    • Tizzano, P.J.1    Griffey, K.I.2    Schoepp, D.D.3
  • 54
    • 0032968641 scopus 로고    scopus 로고
    • The selective mGlR2/3 receptor agonist LY354740 attenuates morphine-withdrawal-induced activation of locus coeruleus neurons and behavioral signs of morphine withdrawal
    • Vardergriff, J.; Rasmussen, K. The selective mGlR2/3 receptor agonist LY354740 attenuates morphine-withdrawal-induced activation of locus coeruleus neurons and behavioral signs of morphine withdrawal. Neuropharmacology 1999, 38, 217-222.
    • (1999) Neuropharmacology , vol.38 , pp. 217-222
    • Vardergriff, J.1    Rasmussen, K.2
  • 55
    • 0033981186 scopus 로고    scopus 로고
    • Physiological Antagonism between 5-Hydroxy-tryptamine 2A and Group II Metabotropic Glutamate Receptors in Prefrontal Cortex
    • (a) Marek, G. J.; Wright, R. A.; Schoepp, D. D.; Monn, J. A.; Aghajanian, G. K. Physiological Antagonism between 5-Hydroxy-tryptamine 2A and Group II Metabotropic Glutamate Receptors in Prefrontal Cortex. J. Pharmacol. Exp. Ther. 2000, 292 (1), 76-87.
    • (2000) J. Pharmacol. Exp. Ther. , vol.292 , Issue.1 , pp. 76-87
    • Marek, G.J.1    Wright, R.A.2    Schoepp, D.D.3    Monn, J.A.4    Aghajanian, G.K.5
  • 56
    • 0033797463 scopus 로고    scopus 로고
    • Behavioral Evidence for Interactions between a Hallucinogenic Drug and Group II Metabotropic Glutamate Receptors
    • (b) Gewirtz, J. C.; Marek, G. J. Behavioral Evidence for Interactions between a Hallucinogenic Drug and Group II Metabotropic Glutamate Receptors. Neuropsychopharmacology 2000, 23 (5), 569-576.
    • (2000) Neuropsychopharmacology , vol.23 , Issue.5 , pp. 569-576
    • Gewirtz, J.C.1    Marek, G.J.2
  • 57
    • 0035996477 scopus 로고    scopus 로고
    • Modulation of DOI-induced increases in cortical BDNF expression by group II mGlu receptors
    • (c) Gewirtz, J. C.; Chen, A. C.; Terwilliger, R.; Duman, R. C.; Marek, G. J. Modulation of DOI-induced increases in cortical BDNF expression by group II mGlu receptors. Pharmacol., Biochem. Behav. 2002, 73, 317-326.
    • (2002) Pharmacol., Biochem. Behav. , vol.73 , pp. 317-326
    • Gewirtz, J.C.1    Chen, A.C.2    Terwilliger, R.3    Duman, R.C.4    Marek, G.J.5
  • 58
    • 0035996485 scopus 로고    scopus 로고
    • Group II mGlu receptor agonists inhibit behavioural and electrophysiological effects of DOI in mice
    • (d) Klodzinska, A.; Bijak, M.; Tokarski, K. Pilc, A. Group II mGlu receptor agonists inhibit behavioural and electrophysiological effects of DOI in mice. Pharmacol., Biochem. Behav. 2002, 73, 327-332.
    • (2002) Pharmacol., Biochem. Behav. , vol.73 , pp. 327-332
    • Klodzinska, A.1    Bijak, M.2    Tokarski, K.3    Pilc, A.4
  • 61
    • 0031786473 scopus 로고    scopus 로고
    • Selective Activation of Group II Metabotropic Glutamate Receptors is Protective Against Excitotoxic Neuronal Death
    • (b) Batagglia, G.; Bruno, V.; Ngomba, R. T.; Di Grezia, R.; Copani, A.; Nicoletti, F. Selective Activation of Group II Metabotropic Glutamate Receptors is Protective Against Excitotoxic Neuronal Death. Eur. J. Pharmacol. 1998, 356, 271-274.
    • (1998) Eur. J. Pharmacol. , vol.356 , pp. 271-274
    • Batagglia, G.1    Bruno, V.2    Ngomba, R.T.3    Di Grezia, R.4    Copani, A.5    Nicoletti, F.6
  • 62
    • 0032566556 scopus 로고    scopus 로고
    • Effects of the Selective Metabotropic Glutamate Agonist LY354740 in a Rat Model of Permanent Ischaemia
    • (c) Lam, A. G. M.; Soriano, M. A.; Monn, J. A.; Schoepp, D. D.; Lodge, D.; McCulloch, J. Effects of the Selective Metabotropic Glutamate Agonist LY354740 in a Rat Model of Permanent Ischaemia. Neurosci. Lett. 1998, 254, 121-123.
    • (1998) Neurosci. Lett. , vol.254 , pp. 121-123
    • Lam, A.G.M.1    Soriano, M.A.2    Monn, J.A.3    Schoepp, D.D.4    Lodge, D.5    McCulloch, J.6
  • 64
    • 0033576789 scopus 로고    scopus 로고
    • Protection of Neonatal Rat Brain from Hypoxic-ischemic Injury by LY379268, a Group II Metabotropic Glutamate Receptor Agonist
    • (e) Cai, Z.; Xiao, F.; Fratkin, J. D.; Rhodes, P. G. Protection of Neonatal Rat Brain from Hypoxic-ischemic Injury by LY379268, a Group II Metabotropic Glutamate Receptor Agonist. Neurochem. Int. 1999, 10, 3927-3931.
    • (1999) Neurochem. Int. , vol.10 , pp. 3927-3931
    • Cai, Z.1    Xiao, F.2    Fratkin, J.D.3    Rhodes, P.G.4
  • 65
    • 0032791811 scopus 로고    scopus 로고
    • Neuroprotection by Metabotropic Glutamate Receptor Agonists: LY354740, LY379268 and LY389795
    • (f) Kingston, A. E.; O'Neill, Lam, A.; Bales, K. R.; Monn, J. A.; Schoepp, D. D. Neuroprotection by Metabotropic Glutamate Receptor Agonists: LY354740, LY379268 and LY389795. Eur. J. Pharmacol. 1999, 377, 155-165.
    • (1999) Eur. J. Pharmacol. , vol.377 , pp. 155-165
    • Kingston, A.E.1    O'Neill2    Lam, A.3    Bales, K.R.4    Monn, J.A.5    Schoepp, D.D.6
  • 66
    • 0033976804 scopus 로고    scopus 로고
    • Neuroprotection by Metabotropic Glutamate Receptor Agonists on Kainate-Induced Degeneration of Motor Neuron in Spinal Cord Slices from Adult Rat
    • (g) Pizzi, M.; Benarese, M.; Boroni, F.; Goffi, F.; Valerio, A.; Spano, P. F. Neuroprotection by Metabotropic Glutamate Receptor Agonists on Kainate-Induced Degeneration of Motor Neuron in Spinal Cord Slices from Adult Rat. Neuropharmacology 2000, 39, 903-910.
    • (2000) Neuropharmacology , vol.39 , pp. 903-910
    • Pizzi, M.1    Benarese, M.2    Boroni, F.3    Goffi, F.4    Valerio, A.5    Spano, P.F.6
  • 68
    • 0035191649 scopus 로고    scopus 로고
    • Involvement of metabotropic glutamate receptors in excitatory amino acid and GABA release following spinal cord injury in rat
    • (i) Mills, C. D.; Xu, G. Y.; McAdoo, D. J.; Hulsebosch, C. E. involvement of metabotropic glutamate receptors in excitatory amino acid and GABA release following spinal cord injury in rat. J. Neurochem. 2001, 79, 835-848.
    • (2001) J. Neurochem. , vol.79 , pp. 835-848
    • Mills, C.D.1    Xu, G.Y.2    McAdoo, D.J.3    Hulsebosch, C.E.4
  • 69
    • 0034073487 scopus 로고    scopus 로고
    • Behavioural evidence supporting a differential role for group I and II metabotropic glutamate receptors in spinal nociceptive transmission
    • (a) Dolan, S.; Nolan, A. M. Behavioural evidence supporting a differential role for group I and II metabotropic glutamate receptors in spinal nociceptive transmission. Neuropharmacology 2000, 39, 1132-1138.
    • (2000) Neuropharmacology , vol.39 , pp. 1132-1138
    • Dolan, S.1    Nolan, A.M.2
  • 70
    • 0033975262 scopus 로고    scopus 로고
    • Periaqueductal gray matter metabotropic glutamate receptors modulate formalin-induced nociception
    • (b) Maione, S.; Oliva, P.; Marabese, I.; Palazzo, E.; Rossi, F.; Berrino, L.; Rossi, F.; Filippelli, A. Periaqueductal gray matter metabotropic glutamate receptors modulate formalin-induced nociception. Pain 2000, 85, 183-189.
    • (2000) Pain , vol.85 , pp. 183-189
    • Maione, S.1    Oliva, P.2    Marabese, I.3    Palazzo, E.4    Rossi, F.5    Berrino, L.6    Rossi, F.7    Filippelli, A.8
  • 71
    • 0033914156 scopus 로고    scopus 로고
    • Selective agonist of group II glutamate metabotropic receptors, LY354740, inhibits tolerance to analgesic effects of morphine in mice
    • (c) Popik, P.; Kozela, E.; Pilc, A. Selective agonist of group II glutamate metabotropic receptors, LY354740, inhibits tolerance to analgesic effects of morphine in mice. Br. J. Pharmacol. 2000, 130, 1425-1431.
    • (2000) Br. J. Pharmacol. , vol.130 , pp. 1425-1431
    • Popik, P.1    Kozela, E.2    Pilc, A.3
  • 73
    • 0033961790 scopus 로고    scopus 로고
    • L-Glutamate Suppresses Amyloid β-Protein-Induced Stellation of Cultured Rat Cortical Astrocytes
    • Abe, K.; Saito, H. L-Glutamate Suppresses Amyloid β-Protein-Induced Stellation of Cultured Rat Cortical Astrocytes. J. Neurochem. 2000, 74 (1), 280-286.
    • (2000) J. Neurochem. , vol.74 , Issue.1 , pp. 280-286
    • Abe, K.1    Saito, H.2
  • 74
    • 0028787326 scopus 로고
    • Blockade of both epileptogenesis and glutamate release by (1S, 3S)-ACPD, a presynaptic glutamate receptor agonist
    • (a) Attwell, P. J. E.; Kaura, S.; Sigala, G.; Bradford, H. F.; Croucher, M. J.; Jane, D. E.; Watkins, J. C. Blockade of both epileptogenesis and glutamate release by (1S, 3S)-ACPD, a presynaptic glutamate receptor agonist. Brain Res. 1995, 698, 155-162.
    • (1995) Brain Res. , vol.698 , pp. 155-162
    • Attwell, P.J.E.1    Kaura, S.2    Sigala, G.3    Bradford, H.F.4    Croucher, M.J.5    Jane, D.E.6    Watkins, J.C.7
  • 75
    • 0030981404 scopus 로고    scopus 로고
    • Anti-epileptogenic and anticonvulsant activity of L-2-amino-4-phosphonobutyrate, a presynaptic glutamate receptor agonist
    • (b) Abdul-Ghani, A. S.; Attwell, P. J. E.; Kent, N. S.; Bradford, H. F.; Croucher, M. J.; Jane, D. E. Anti-epileptogenic and anticonvulsant activity of L-2-amino-4-phosphonobutyrate, a presynaptic glutamate receptor agonist. Brain Res. 1997, 755, 202-212.
    • (1997) Brain Res. , vol.755 , pp. 202-212
    • Abdul-Ghani, A.S.1    Attwell, P.J.E.2    Kent, N.S.3    Bradford, H.F.4    Croucher, M.J.5    Jane, D.E.6
  • 76
    • 0342545860 scopus 로고    scopus 로고
    • Selective group II glutamate metabotropic receptor agonist LY354740 attenuates pentetrazole- and picrotoxin-induced seizures
    • (c) Klodzinska, A.; Chojnacka-Wojcik, E.; Pilc, A. Selective group II glutamate metabotropic receptor agonist LY354740 attenuates pentetrazole- and picrotoxin-induced seizures. Pol. J. Pharmacol. 1999, 51, 543-545.
    • (1999) Pol. J. Pharmacol. , vol.51 , pp. 543-545
    • Klodzinska, A.1    Chojnacka-Wojcik, E.2    Pilc, A.3
  • 77
    • 0034964561 scopus 로고    scopus 로고
    • Anti-epileptic activity of group II metabotropic glutamate receptor agonists (-)-2-oxa-4-aminobicyclo[3.1.0.]-hexane-4,6-dicarboxylate (LY389795)
    • (d) Moldrich, R. X.; Jeffrey, M.; Talebi, A.; Beart, P. M.; Chapman, A. G.; Meldrum, B. S. Anti-epileptic activity of group II metabotropic glutamate receptor agonists (-)-2-oxa-4-aminobicyclo[3.1.0.]-hexane-4,6-dicarboxylate (LY389795). Neuropharmacology 2001, 41, 8-18.
    • (2001) Neuropharmacology , vol.41 , pp. 8-18
    • Moldrich, R.X.1    Jeffrey, M.2    Talebi, A.3    Beart, P.M.4    Chapman, A.G.5    Meldrum, B.S.6
  • 78
    • 0031689603 scopus 로고    scopus 로고
    • LY354740, a group 2 metabotropic glutamate receptor agonist with potential antiparkinsonian properties in rats
    • (a) Konieczny, J.; Ossowska, K.; Wolfarth, S.; Pilc, A. LY354740, a group 2 metabotropic glutamate receptor agonist with potential antiparkinsonian properties in rats. Naunyn-Schmiedeberg's Arch. Pharmacol. 1998, 358, 500-502.
    • (1998) Naunyn-Schmiedeberg's Arch. Pharmacol. , vol.358 , pp. 500-502
    • Konieczny, J.1    Ossowska, K.2    Wolfarth, S.3    Pilc, A.4
  • 79
    • 0033796468 scopus 로고    scopus 로고
    • The role of metabotropic glutamate receptor (mGluR) ligands in parkinsonian muscle rigidity
    • (b) Wolfarth, S.; Konieczny, J.; Lorenc-Koci, E.; Ossowska, K.; Pilc, A. The role of metabotropic glutamate receptor (mGluR) ligands in parkinsonian muscle rigidity. Amino Acids 2000, 19, 95-101.
    • (2000) Amino Acids , vol.19 , pp. 95-101
    • Wolfarth, S.1    Konieczny, J.2    Lorenc-Koci, E.3    Ossowska, K.4    Pilc, A.5
  • 80
    • 0035067196 scopus 로고    scopus 로고
    • Glutamatergic Influences on the Basal Ganglia
    • (c) Greenamyre, J. P. Glutamatergic Influences on the Basal Ganglia. Clin. Neuropharmacol. 2001, 24 (2), 65-70.
    • (2001) Clin. Neuropharmacol. , vol.24 , Issue.2 , pp. 65-70
    • Greenamyre, J.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.