-
1
-
-
0026596597
-
Signal transduction and pharmacological characteristics of a metabotropic glutamate receptor, mgluR1, in transfected CHO cells
-
I. Aramori, and S. Nakanishi Signal transduction and pharmacological characteristics of a metabotropic glutamate receptor, mgluR1, in transfected CHO cells Neuron 8 1992 757 765
-
(1992)
Neuron
, vol.8
, pp. 757-765
-
-
Aramori, I.1
Nakanishi, S.2
-
2
-
-
0000189651
-
Density-functional thermochemistry: III. the role of exact exchange
-
A.D. Becke Density-functional thermochemistry: III. The role of exact exchange J. Chem. Phys. 98 1993 5648 5652
-
(1993)
J. Chem. Phys.
, vol.98
, pp. 5648-5652
-
-
Becke, A.D.1
-
3
-
-
0037143619
-
Closure of the Venus flytrap module of mGlu8 receptor and the activation process: Insights from mutations converting antagonists into agonists
-
A.S. Bessis, P. Rondard, F. Gaven, I. Brabet, N. Triballeau, L. Prezeau, F. Acher, and J.P. Pin Closure of the Venus flytrap module of mGlu8 receptor and the activation process: insights from mutations converting antagonists into agonists PNAS 97 2002 11097 11102
-
(2002)
PNAS
, vol.97
, pp. 11097-11102
-
-
Bessis, A.S.1
Rondard, P.2
Gaven, F.3
Brabet, I.4
Triballeau, N.5
Prezeau, L.6
Acher, F.7
Pin, J.P.8
-
4
-
-
0038366553
-
Design, synthesis, and pharmacology of a highly subtype-selective GluR1/2 agonist, (RS)-2-amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic acid (Cl-HIBO)
-
E.J. Bjerrum, A.S. Kristensen, D.S. Pickering, J.R. Greenwood, B. Nielsen, T. Liljefors, A. Schousboe, H. Bräuner-Osborne, and U. Madsen Design, synthesis, and pharmacology of a highly subtype-selective GluR1/2 agonist, (RS)-2-amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic acid (Cl-HIBO) J. Med. Chem. 46 2003 2246 2249
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2246-2249
-
-
Bjerrum, E.J.1
Kristensen, A.S.2
Pickering, D.S.3
Greenwood, J.R.4
Nielsen, B.5
Liljefors, T.6
Schousboe, A.7
Bräuner-Osborne, H.8
Madsen, U.9
-
5
-
-
0023162156
-
3H]kainic acid receptor binding by divalent cations correlates with ion affinity for the calcium channel
-
3H]kainic acid receptor binding by divalent cations correlates with ion affinity for the calcium channel Neuropharmacology 26 1987 1247 1251
-
(1987)
Neuropharmacology
, vol.26
, pp. 1247-1251
-
-
Braitman, D.J.1
Coyle, J.T.2
-
6
-
-
0031985230
-
Pharmacology of (S)-homoquisqualic acid and (S)-2-amino-5- phosphonopentanoic acid [(S)-AP5] at cloned metabotropic glutamate receptors
-
H. Bräuner-Osborne, and P. Krogsgaard-Larsen Pharmacology of (S)-homoquisqualic acid and (S)-2-amino-5-phosphonopentanoic acid [(S)-AP5] at cloned metabotropic glutamate receptors Br. J. Pharmacol. 123 1998 269 274
-
(1998)
Br. J. Pharmacol.
, vol.123
, pp. 269-274
-
-
Bräuner-Osborne, H.1
Krogsgaard-Larsen, P.2
-
7
-
-
0029742345
-
A new highly selective metabotropic excitatory amino acid agonist: 2-amino-4-(3-hydroxy-5-methylisoxazol-4-yl)butyric acid
-
H. Bräuner-Osborne, F.A. Sløk, N. Skjærbæk, B. Ebert, N. Sekiyama, S. Nakanishi, and P. Krogsgaard-Larsen A new highly selective metabotropic excitatory amino acid agonist: 2-amino-4-(3-hydroxy-5- methylisoxazol-4-yl)butyric acid J. Med. Chem. 39 1996 3188 3194
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3188-3194
-
-
Bräuner-Osborne, H.1
Sløk, F.A.2
Skjærbæk, N.3
Ebert, B.4
Sekiyama, N.5
Nakanishi, S.6
Krogsgaard-Larsen, P.7
-
8
-
-
0037832971
-
Ligands for glutamate receptors: Design and therapeutic prospects
-
H. Bräuner-Osborne, J. Egebjerg, E.Ø. Nielsen, U. Madsen, and P. Krogsgaard-Larsen Ligands for glutamate receptors: design and therapeutic prospects J. Med. Chem. 43 2000 2609 2645
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2609-2645
-
-
Bräuner-Osborne, H.1
Egebjerg, J.2
Nielsen E.Ø3
Madsen, U.4
Krogsgaard-Larsen, P.5
-
9
-
-
0037127757
-
Synthesis of 1-hydroxypyrazole glycine derivatives
-
P. Cali, and M. Begtrup Synthesis of 1-hydroxypyrazole glycine derivatives Tetrahedron 58 2002 1595 1605
-
(2002)
Tetrahedron
, vol.58
, pp. 1595-1605
-
-
Cali, P.1
Begtrup, M.2
-
10
-
-
0035826004
-
Comment on "reaction field treatment of charge penetration"
-
E. Cancès, and B. Mennucci Comment on "Reaction field treatment of charge penetration" J. Chem. Phys. 114 2001 4744 4745
-
(2001)
J. Chem. Phys.
, vol.114
, pp. 4744-4745
-
-
Cancès, E.1
Mennucci, B.2
-
11
-
-
0015861774
-
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
Y. Cheng, and W.H. Prusoff Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction Biochem. Pharmacol. 22 1973 3099 3108
-
(1973)
Biochem. Pharmacol.
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
12
-
-
0030995878
-
Pharmacology and functions of metabotropic glutamate receptors
-
P.J. Conn, and J.P. Pin Pharmacology and functions of metabotropic glutamate receptors Annu. Rev. Pharmacol. Toxicol. 37 1997 205 237
-
(1997)
Annu. Rev. Pharmacol. Toxicol.
, vol.37
, pp. 205-237
-
-
Conn, P.J.1
Pin, J.P.2
-
14
-
-
5544242529
-
MMFF: VI. MMFF94s option for energy minimization studies
-
T.A. Halgren MMFF: VI. MMFF94s option for energy minimization studies J. Comp. Chem. 20 1999 720 729
-
(1999)
J. Comp. Chem.
, vol.20
, pp. 720-729
-
-
Halgren, T.A.1
-
15
-
-
0001242234
-
MMFF: VII. Characterization of MMFF94, MMFF94s, and other widely available force fields for conformational energies and for intermolecular- interaction energies and geometries
-
T.A. Halgren MMFF: VII. Characterization of MMFF94, MMFF94s, and other widely available force fields for conformational energies and for intermolecular-interaction energies and geometries J. Comp. Chem. 20 1999 730 748
-
(1999)
J. Comp. Chem.
, vol.20
, pp. 730-748
-
-
Halgren, T.A.1
-
16
-
-
10744221953
-
Ibotenic acid and thioibotenic acid: A remarkable difference in activity at group III metabotropic glutamate receptors
-
M.B. Hermit, J.R. Greenwood, B. Nielsen, L. Bunch, C.G. Jørgensen, H.T. Vestergaard, T.B. Stensbøl, C. Sanchez, P. Krogsgaard-Larsen, U. Madsen, and H. Bräuner-Osborne Ibotenic acid and thioibotenic acid: a remarkable difference in activity at group III metabotropic glutamate receptors Eur. J. Pharmacol. 486 2004 241 250
-
(2004)
Eur. J. Pharmacol.
, vol.486
, pp. 241-250
-
-
Hermit, M.B.1
Greenwood, J.R.2
Nielsen, B.3
Bunch, L.4
Jørgensen, C.G.5
Vestergaard, H.T.6
Stensbøl, T.B.7
Sanchez, C.8
Krogsgaard-Larsen, P.9
Madsen, U.10
Bräuner-Osborne, H.11
-
17
-
-
0036968894
-
Structural basis for AMPA receptor activation and ligand selectivity: Crystal structures of five agonist complexes with the GluR2 ligand-binding core
-
A. Hogner, J. Kastrup, R. Jin, T. Liljefors, M. Mayer, J. Egebjerg, I. Larsen, and E. Gouaux Structural basis for AMPA receptor activation and ligand selectivity: crystal structures of five agonist complexes with the GluR2 ligand-binding core J. Mol. Biol. 322 2002 93
-
(2002)
J. Mol. Biol.
, vol.322
, pp. 93
-
-
Hogner, A.1
Kastrup, J.2
Jin, R.3
Liljefors, T.4
Mayer, M.5
Egebjerg, J.6
Larsen, I.7
Gouaux, E.8
-
18
-
-
0345059225
-
Metabotropic glutamate receptor activation and blockade: Their role in long-term potentiation, learning and neurotoxicity
-
C. Holscher, J. Gigg, and S.M. O'Mara Metabotropic glutamate receptor activation and blockade: their role in long-term potentiation, learning and neurotoxicity Neurosci. Biobehav. Rev. 23 1999 399 410
-
(1999)
Neurosci. Biobehav. Rev.
, vol.23
, pp. 399-410
-
-
Holscher, C.1
Gigg, J.2
O'Mara, S.M.3
-
19
-
-
0021991131
-
Complex structure of quisqualate-sensitive glutamate receptors in rat cortex
-
T. Honore, and M. Nielsen Complex structure of quisqualate-sensitive glutamate receptors in rat cortex Neurosci. Lett. 54 1985 27 32
-
(1985)
Neurosci. Lett.
, vol.54
, pp. 27-32
-
-
Honore, T.1
Nielsen, M.2
-
20
-
-
0036234291
-
2-Amino-3-(3-hydroxy-1,2,5-thiadiazol-4-yl)propionic acid: Resolution, absolute stereochemistry and enantiopharmacology at glutamate receptors
-
T.N. Johansen, Y.L. Janin, B. Nielsen, K. Frydenvang, H. Bräuner-Osborne, T.B. Stensbøl, S.B. Vogensen, U. Madsen, and P. Krogsgaard-Larsen 2-Amino-3-(3-hydroxy-1,2,5-thiadiazol-4-yl)propionic acid: resolution, absolute stereochemistry and enantiopharmacology at glutamate receptors Bioorg. Med. Chem. 10 2002 2259 2266
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 2259-2266
-
-
Johansen, T.N.1
Janin, Y.L.2
Nielsen, B.3
Frydenvang, K.4
Bräuner-Osborne, H.5
Stensbøl, T.B.6
Vogensen, S.B.7
Madsen, U.8
Krogsgaard-Larsen, P.9
-
21
-
-
26844534384
-
Self-consistent molecular-orbital methods: XX. Basis set for correlated wave-functions
-
R. Krishnan, J.S. Binkley, R. Seeger, and J.A. Pople Self-consistent molecular-orbital methods: XX. Basis set for correlated wave-functions J. Chem. Phys. 72 1980 650 654
-
(1980)
J. Chem. Phys.
, vol.72
, pp. 650-654
-
-
Krishnan, R.1
Binkley, J.S.2
Seeger, R.3
Pople, J.A.4
-
22
-
-
0026676888
-
Naturally-occurring excitatory amino acids as neurotoxins and leads in drug design
-
P. Krogsgaard-Larsen, and J.J. Hansen Naturally-occurring excitatory amino acids as neurotoxins and leads in drug design Toxicol. Lett. 1992 64 65 (Spec. No. 409-416)
-
(1992)
Toxicol. Lett.
, pp. 64-65
-
-
Krogsgaard-Larsen, P.1
Hansen, J.J.2
-
23
-
-
0025204045
-
NMDA receptor agonists derived from ibotenic acid. Preparation, neuroexcitation and neurotoxicity
-
U. Madsen, J.W. Ferkany, B.E. Jones, B. Ebert, T.N. Johansen, T. Holm, and P. Krogsgaard-Larsen NMDA receptor agonists derived from ibotenic acid. Preparation, neuroexcitation and neurotoxicity Eur. J. Pharmacol., Mol. Pharmacol. 189 1990 381 391
-
(1990)
Eur. J. Pharmacol., Mol. Pharmacol.
, vol.189
, pp. 381-391
-
-
Madsen, U.1
Ferkany, J.W.2
Jones, B.E.3
Ebert, B.4
Johansen, T.N.5
Holm, T.6
Krogsgaard-Larsen, P.7
-
24
-
-
0034759133
-
Identification of essential residues involved in the glutamate binding pocket of the group II metabotropic glutamate receptor
-
P. Malherbe, F. Knoflach, C. Broger, S. Ohresser, C. Kratzeisen, G. Adam, H. Stadler, J.A. Kemp, and V. Mutel Identification of essential residues involved in the glutamate binding pocket of the group II metabotropic glutamate receptor Mol. Pharmacol. 60 2001 944 954
-
(2001)
Mol. Pharmacol.
, vol.60
, pp. 944-954
-
-
Malherbe, P.1
Knoflach, F.2
Broger, C.3
Ohresser, S.4
Kratzeisen, C.5
Adam, G.6
Stadler, H.7
Kemp, J.A.8
Mutel, V.9
-
25
-
-
0023820777
-
3H]MK-801 binding to the N-methyl-d-aspartate receptor-ion channel complex by l-glutamate, glycine, and polyamines
-
3H]MK-801 binding to the N-methyl-d-aspartate receptor-ion channel complex by l-glutamate, glycine, and polyamines J. Neurochem. 51 1988 830 836
-
(1988)
J. Neurochem.
, vol.51
, pp. 830-836
-
-
Ransom, R.W.1
Stec, N.L.2
-
26
-
-
0037452854
-
Glutamate receptor function in learning and memory
-
G. Riedel, B. Platt, and J. Micheau Glutamate receptor function in learning and memory Behav. Brain Res. 140 2003 1 47
-
(2003)
Behav. Brain Res.
, vol.140
, pp. 1-47
-
-
Riedel, G.1
Platt, B.2
Micheau, J.3
-
27
-
-
0036510646
-
Molecular determinants of high affinity binding to group III metabotropic glutamate receptors
-
E. Rosemond, V. Peltekova, M. Naples, H. Thøgersen, and D.R. Hampson Molecular determinants of high affinity binding to group III metabotropic glutamate receptors J. Biol. Chem. 277 2002 7333 7340
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 7333-7340
-
-
Rosemond, E.1
Peltekova, V.2
Naples, M.3
Thøgersen, H.4
Hampson, D.R.5
-
28
-
-
0037423395
-
Amino acid mutagenesis of the ligand binding site and the dimer interface of the metabotropic glutamate receptor 1. Identification of crucial residues for setting the activated state
-
T. Sato, Y. Shimada, N. Nagasawa, S. Nakanishi, and H. Jingami Amino acid mutagenesis of the ligand binding site and the dimer interface of the metabotropic glutamate receptor 1. Identification of crucial residues for setting the activated state J. Biol. Chem. 278 2003 4314 4321
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4314-4321
-
-
Sato, T.1
Shimada, Y.2
Nagasawa, N.3
Nakanishi, S.4
Jingami, H.5
-
29
-
-
0025924039
-
3H]CGP 39653: A new N-methyl-d-aspartate antagonist radioligand with low nanomolar affinity in rat brain
-
3H]CGP 39653: a new N-methyl-d-aspartate antagonist radioligand with low nanomolar affinity in rat brain Eur. J. Pharmacol. 192 1991 19 24
-
(1991)
Eur. J. Pharmacol.
, vol.192
, pp. 19-24
-
-
Sills, M.A.1
Fagg, G.2
Pozza, M.3
Angst, C.4
Brundish, D.E.5
Hurt, S.D.6
Wilusz, E.J.7
Williams, M.8
-
30
-
-
0037011909
-
Novel 1-hydroxyazole bioisosteres of glutamic acid. Synthesis, protolytic properties, and pharmacology
-
T.B. Stensbøl, P. Uhlmann, S. Morel, B.L. Eriksen, J. Felding, H. Kromann, M.B. Hermit, J.R. Greenwood, H. Bräuner-Osborne, U. Madsen, F. Junager, P. Krogsgaard-Larsen, M. Begtrup, and P. Vedsø Novel 1-hydroxyazole bioisosteres of glutamic acid. Synthesis, protolytic properties, and pharmacology J. Med. Chem. 45 2002 19 31
-
(2002)
J. Med. Chem.
, vol.45
, pp. 19-31
-
-
Stensbøl, T.B.1
Uhlmann, P.2
Morel, S.3
Eriksen, B.L.4
Felding, J.5
Kromann, H.6
Hermit, M.B.7
Greenwood, J.R.8
Bräuner-Osborne, H.9
Madsen, U.10
Junager, F.11
Krogsgaard-Larsen, P.12
Begtrup, M.13
Vedsø, P.14
-
31
-
-
0026593238
-
A family of metabotropic glutamate receptors
-
Y. Tanabe, M. Masu, T. Ishii, R. Shigemoto, and S. Nakanishi A family of metabotropic glutamate receptors Neuron 8 1992 169 179
-
(1992)
Neuron
, vol.8
, pp. 169-179
-
-
Tanabe, Y.1
Masu, M.2
Ishii, T.3
Shigemoto, R.4
Nakanishi, S.5
-
32
-
-
0027410488
-
Signal transduction, pharmacological properties, and expression patterns of two rat metabotropic glutamate receptors, mgluR3 and mgluR4
-
Y. Tanabe, A. Nomura, M. Masu, R. Shigemoto, N. Mizuno, and S. Nakanishi Signal transduction, pharmacological properties, and expression patterns of two rat metabotropic glutamate receptors, mgluR3 and mgluR4 J. Neurosci. 13 1993 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
|