-
1
-
-
0028340001
-
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
-
2
-
-
0035504328
-
J. structural, signaling and regulatory properties of the group I metabotropic glutamate receptors: Protypic family C G-protein-coupled receptors
-
(b) Hermans, E.; Challiss, R. A. J. structural, signaling and regulatory properties of the group I metabotropic glutamate receptors: protypic family C G-protein-coupled receptors. Biochem. J. 2001, 359, 465-484.
-
(2001)
Biochem. J
, vol.359
, pp. 465-484
-
-
Hermans, E.1
Challiss, R.A.2
-
3
-
-
0032834028
-
Pharmacological agents acting at subtypes of metabotropic glutamate receptors
-
(a) 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
-
4
-
-
11144298072
-
mGluR1 and mGluR5 antagonists in the amygdale inhibit different components of audible and ultrasonic vocalizations in a model of arthritic pain
-
(b) Han, J. S.; Neugebauer, V. mGluR1 and mGluR5 antagonists in the amygdale inhibit different components of audible and ultrasonic vocalizations in a model of arthritic pain. Pain 2005, 113, 211-222.
-
(2005)
Pain
, vol.113
, pp. 211-222
-
-
Han, J.S.1
Neugebauer, V.2
-
5
-
-
0035094199
-
Peripheral group I metabotropic glutamate receptors modulate nociception in mice
-
(a) Bhave, G.; Karim, F.; Carlton, S. M.; Gereau, R. W., IV. Peripheral group I metabotropic glutamate receptors modulate nociception in mice. Nat. Neurosci. 2001, 4, 417-423.
-
(2001)
Nat. Neurosci
, vol.4
, pp. 417-423
-
-
Bhave, G.1
Karim, F.2
Carlton, S.M.3
Gereau, R.4
IV, W.5
-
7
-
-
0344305540
-
-
(c) Dolan, S.; Kelly, J. G.; Monteiro, A. M.; Nolan, A. M. Pain 2003, 106, 501-512.
-
(2003)
Pain
, vol.106
, pp. 501-512
-
-
Dolan, S.1
Kelly, J.G.2
Monteiro, A.M.3
Nolan, A.M.4
-
8
-
-
0028350254
-
Evidence for a role of metabotropic glutamate receptors in sustained nociceptive inputs to rat dorsal horn neurons
-
(d) Young, M. R.; Fleetwood-Walker, S. M.; Mitchell, R.; Munro, F. E. Evidence for a role of metabotropic glutamate receptors in sustained nociceptive inputs to rat dorsal horn neurons. Neuropharmacology 1994, 33, 141-144.
-
(1994)
Neuropharmacology
, vol.33
, pp. 141-144
-
-
Young, M.R.1
Fleetwood-Walker, S.M.2
Mitchell, R.3
Munro, F.E.4
-
9
-
-
0031589694
-
Behavoiral and electrophysiological evidence supporting a role for group I metabotropic glutamate receptors in the mediation of nociceptive inputs to the rat spinal cord
-
(e) Young, M. R.; Fleetwood-Walker, S. M.; Dickinson, T.; Blackburn-Munro, G.; Sparrow, H.; Birch, P. J.; Bountra, C. Behavoiral and electrophysiological evidence supporting a role for group I metabotropic glutamate receptors in the mediation of nociceptive inputs to the rat spinal cord. Brain Res. 1997, 777, 161-169.
-
(1997)
Brain Res
, vol.777
, pp. 161-169
-
-
Young, M.R.1
Fleetwood-Walker, S.M.2
Dickinson, T.3
Blackburn-Munro, G.4
Sparrow, H.5
Birch, P.J.6
Bountra, C.7
-
10
-
-
0035478759
-
Peripheral metabotropic glutamate receptors: Fight the pain where it hurts
-
Neugebauer, V. Peripheral metabotropic glutamate receptors: fight the pain where it hurts. Trends Neurosci. 2001, 24, 550-552.
-
(2001)
Trends Neurosci
, vol.24
, pp. 550-552
-
-
Neugebauer, V.1
-
11
-
-
0036085243
-
Peripheral metabotropic glutamate receptors as drug targets for pain relief
-
(a) Neugebauer, V.; Carlton, S. M. Peripheral metabotropic glutamate receptors as drug targets for pain relief. Expert Opin. Ther. Targets 2002, 6, 349-361.
-
(2002)
Expert Opin. Ther. Targets
, vol.6
, pp. 349-361
-
-
Neugebauer, V.1
Carlton, S.M.2
-
12
-
-
14044258729
-
Metobotropic glutamate receptors as novel targets for anxiety and stress disorders
-
(b) Swanson, C. J.; Bures, M.; Johnson, M. P.; Linden, A.-M.; Monn, J. A.; Schoepp, D. D. Metobotropic glutamate receptors as novel targets for anxiety and stress disorders. Nat. Rev. Drug Discovery 2005, 4, 131-144.
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, pp. 131-144
-
-
Swanson, C.J.1
Bures, M.2
Johnson, M.P.3
Linden, A.-M.4
Monn, J.A.5
Schoepp, D.D.6
-
13
-
-
36148980313
-
-
Ambler, S. J.; Baker, S. R.; Clark, B. P.; Coleman, D. S.; Foglesong, R. J.; Goldsworthy, J. Jagdmann, G. K., Jr.; Johnson, K. W.; Kingston, A. E.; Owton, W. M.; Schoepp, D. D.; Hong, J. E.; Schkeryantz, J. M.; Vannieuwenhze, M. S.; Zia-ebrahimi, M. S. Preparation of heterocycles containing a 4-substituted pyrimidine subunit for pharmaceutical use as mGluR1 antagonists. WO 2001032632, 2001.
-
(a) Ambler, S. J.; Baker, S. R.; Clark, B. P.; Coleman, D. S.; Foglesong, R. J.; Goldsworthy, J. Jagdmann, G. K., Jr.; Johnson, K. W.; Kingston, A. E.; Owton, W. M.; Schoepp, D. D.; Hong, J. E.; Schkeryantz, J. M.; Vannieuwenhze, M. S.; Zia-ebrahimi, M. S. Preparation of heterocycles containing a 4-substituted pyrimidine subunit for pharmaceutical use as mGluR1 antagonists. WO 2001032632, 2001.
-
-
-
-
14
-
-
36148995731
-
Preparation of aminomethyl-substituted fluorothiazolobenzimidazole derivatives with affinity for mGluR1 receptors
-
WO 2004106348
-
(b) Itahana, H.; Fujisayu, J.; Watanabe, T.; Okada, M.; Toya, T. Preparation of aminomethyl-substituted fluorothiazolobenzimidazole derivatives with affinity for mGluR1 receptors. WO 2004106348, 2004.
-
(2004)
-
-
Itahana, H.1
Fujisayu, J.2
Watanabe, T.3
Okada, M.4
Toya, T.5
-
15
-
-
20144369074
-
Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGluR1 antagonists
-
(c) Mabire, D.; Coupa, S.; Adeline, C.; Poncelet, A.; Simonnet, Y.; Venet, M.; Wouters, R.; Lesage, A. S. J.; Beijsterveldt, L. V.; Bischoff, F. Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGluR1 antagonists. J. Med. Chem. 2005, 48, 2134-2153.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2134-2153
-
-
Mabire, D.1
Coupa, S.2
Adeline, C.3
Poncelet, A.4
Simonnet, Y.5
Venet, M.6
Wouters, R.7
Lesage, A.S.J.8
Beijsterveldt, L.V.9
Bischoff, F.10
-
16
-
-
28544443384
-
Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists
-
(d) Zheng, G. Z.; Bhatia, P.; Daanen, J.; Kolasa, T.; Patel, M.; Latshaw, S.; Kouhen, O. F. E.; Chang, R.; Uchic, M. E.; Miller, L.; Nakane, M.; Lehto, S. G.; Honore, M. P.; Moreland, R. B.; Brioni, J. D.;Stewart, A. O. Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists. J. Med. Chem. 2005, 48, 7374-7388.
-
(2005)
J. Med. Chem
, vol.48
, pp. 7374-7388
-
-
Zheng, G.Z.1
Bhatia, P.2
Daanen, J.3
Kolasa, T.4
Patel, M.5
Latshaw, S.6
Kouhen, O.F.E.7
Chang, R.8
Uchic, M.E.9
Miller, L.10
Nakane, M.11
Lehto, S.G.12
Honore, M.P.13
Moreland, R.B.14
Brioni, J.D.15
Stewart, A.O.16
-
17
-
-
33846056113
-
Structure-activity relationships of novel non-competitive mGluR1 antagonists: A potent treatment for chronic pain
-
(e) Owen, D. R.; Dodd, P. G.; Gayton, S.; Greener, B. S.; Harbottle, G. W.; Mantell, S. J.; Maw, G. N.; Osborne, S. A.; Rees, H.; Ringer, T. J.; Rodriguez-Lens, M.; Smith, G. F. Structure-activity relationships of novel non-competitive mGluR1 antagonists: a potent treatment for chronic pain. Bioorg. Med Chem. Lett. 2007, 17, 486-490.
-
(2007)
Bioorg. Med Chem. Lett
, vol.17
, pp. 486-490
-
-
Owen, D.R.1
Dodd, P.G.2
Gayton, S.3
Greener, B.S.4
Harbottle, G.W.5
Mantell, S.J.6
Maw, G.N.7
Osborne, S.A.8
Rees, H.9
Ringer, T.J.10
Rodriguez-Lens, M.11
Smith, G.F.12
-
18
-
-
33947572694
-
-
Fabio, R. D.; Micheli, F.; Alvaro, G.; Cavanni, P.; Donati, D.; Gagliardi, T.; Fontana, G.; Giovannini, R.; Maffeis, M.; Mingardi, A.; Tranquillini, M. E.; Vitulli, G. From pyrroles to 1-oxo-2,3,4,9-tetrahydro- 1H-β-carbolines: a new class of orally bioavailable mGluR1 antagonists. Bioorg. Med. Chem. Lett. 2007, 17, 2254-2259.
-
(f) Fabio, R. D.; Micheli, F.; Alvaro, G.; Cavanni, P.; Donati, D.; Gagliardi, T.; Fontana, G.; Giovannini, R.; Maffeis, M.; Mingardi, A.; Tranquillini, M. E.; Vitulli, G. From pyrroles to 1-oxo-2,3,4,9-tetrahydro- 1H-β-carbolines: a new class of orally bioavailable mGluR1 antagonists. Bioorg. Med. Chem. Lett. 2007, 17, 2254-2259.
-
-
-
-
19
-
-
27144543360
-
DMF diethyl acetal as a one-carbon component in the synthesis of isomeric pyridothienopyrimidines
-
(a) Kadushkin, A. V.; Solovyeva, N. P.; Granik, V. G. DMF diethyl acetal as a one-carbon component in the synthesis of isomeric pyridothienopyrimidines. Khim.-Farm. Zh. 1993, 27, 40-43.
-
(1993)
Khim.-Farm. Zh
, vol.27
, pp. 40-43
-
-
Kadushkin, A.V.1
Solovyeva, N.P.2
Granik, V.G.3
-
20
-
-
36148970709
-
-
U.S
-
(b) Matasi, J. J.; Tulshian, D.; Burnett, D. A.; Wu, W.-L.; Korakas, P.; Silverman, L. S.; Sasikumar, T. K.; Qiang, L.; Domalski, M. S. Preparation of tricyclic compounds as mGluR1 antagonists. U.S. 2006167029, 2006.
-
(2006)
Preparation of tricyclic compounds as mGluR1 antagonists
, pp. 2006167029
-
-
Matasi, J.J.1
Tulshian, D.2
Burnett, D.A.3
Wu, W.-L.4
Korakas, P.5
Silverman, L.S.6
Sasikumar, T.K.7
Qiang, L.8
Domalski, M.S.9
-
21
-
-
36148985945
-
-
Compound 6 is obtained from treatment of 12 with excess NBS.
-
Compound 6 is obtained from treatment of 12 with excess NBS.
-
-
-
-
22
-
-
49749179236
-
New conversions of pyridinium salts and synthesis of γ-amino-substituted pyridines
-
Vompe, A. F.; Monitch, N. V.; Turitsyna, N. F.; Ivanova, L. V. New conversions of pyridinium salts and synthesis of γ-amino-substituted pyridines. Tetrahedron 1958, 2, 90-95.
-
(1958)
Tetrahedron
, vol.2
, pp. 90-95
-
-
Vompe, A.F.1
Monitch, N.V.2
Turitsyna, N.F.3
Ivanova, L.V.4
-
23
-
-
0026022044
-
Condensed heteroaromatic ring systems. XVIII. Palladium-catalyzed cross-coupling reaction of aryl bromides with (Z)-1-ethoxy-2-tributylstannylethene and its utilization for construction of condensed heteroaromatics
-
Sakamoto, T.; Kondo, Y.; Yasuhara, A.; Yamanaka, H. Condensed heteroaromatic ring systems. XVIII. Palladium-catalyzed cross-coupling reaction of aryl bromides with (Z)-1-ethoxy-2-tributylstannylethene and its utilization for construction of condensed heteroaromatics. Tetrahedron 1991, 47, 1877-1886.
-
(1991)
Tetrahedron
, vol.47
, pp. 1877-1886
-
-
Sakamoto, T.1
Kondo, Y.2
Yasuhara, A.3
Yamanaka, H.4
-
24
-
-
0025260781
-
Palladium catalyzed cross-coupling of phenol triflates with organostannanes. A versatile approach for the synthesis of substituted resorcinol dimethyl ethers
-
Martorell, G.; Garcia-raco, A.; SAA, J. M. Palladium catalyzed cross-coupling of phenol triflates with organostannanes. A versatile approach for the synthesis of substituted resorcinol dimethyl ethers. Tetrahedron Lett. 1990, 31, 2357-2360.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 2357-2360
-
-
Martorell, G.1
Garcia-raco, A.2
SAA, J.M.3
-
25
-
-
0034336713
-
-
Ozeryanskii, V. A.; Pozharskii, A. F.; Vistorobskii, N. V. Peri-nNaphthylenediamines. 28. Nitration of 1,8-bis(dimethylamino)- naphalene and 5,6-bis(dimethylamino)acenaphthene in neutral and weakly acidic media. The first case of isolation of o-nitro and o,o′- dinitro derivatives of proton sponges. Russ. Chem. Bull. 2000, 49, 1212-1217.
-
Ozeryanskii, V. A.; Pozharskii, A. F.; Vistorobskii, N. V. Peri-nNaphthylenediamines. 28. Nitration of 1,8-bis(dimethylamino)- naphalene and 5,6-bis(dimethylamino)acenaphthene in neutral and weakly acidic media. The first case of isolation of o-nitro and o,o′- dinitro derivatives of "proton sponges". Russ. Chem. Bull. 2000, 49, 1212-1217.
-
-
-
-
26
-
-
0000767168
-
The synthesis of some 4-quinolinols and 4-chloroquinolinolines by the ethoxymethylenemalonic ester method
-
Riegel, B.; Lappin, G. R.; Adelson, B. H.; Jackson, R. I.; Albisetti, C. J., Jr.; Dodson, R. M.; Baker, R. H. The synthesis of some 4-quinolinols and 4-chloroquinolinolines by the ethoxymethylenemalonic ester method. J. Am Chem. Soc. 1946, 68, 1264-1266.
-
(1946)
J. Am Chem. Soc
, vol.68
, pp. 1264-1266
-
-
Riegel, B.1
Lappin, G.R.2
Adelson, B.H.3
Jackson, R.I.4
Albisetti Jr., C.J.5
Dodson, R.M.6
Baker, R.H.7
-
27
-
-
0005155779
-
Synthesis, antimalarial and antibacterial activity of 1-chloro-2-formylcarbazole derivatives and pyrazolo[3,4-a] carbazole derivatives
-
Sekar, M.; Prasad, K. J. R. Synthesis, antimalarial and antibacterial activity of 1-chloro-2-formylcarbazole derivatives and pyrazolo[3,4-a] carbazole derivatives. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1998, 37, 314-317.
-
(1998)
Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem
, vol.37
, pp. 314-317
-
-
Sekar, M.1
Prasad, K.J.R.2
-
28
-
-
3042737375
-
-
Singh, B.; Pennock, P. O.; Lesher, G. Y.; Bacon, E. P.; Page, D. F. An efficient and novel synthesis of fused thiazol-2(3H)-ones. Heterocycles 1993, 36, 133-144.
-
Singh, B.; Pennock, P. O.; Lesher, G. Y.; Bacon, E. P.; Page, D. F. An efficient and novel synthesis of fused thiazol-2(3H)-ones. Heterocycles 1993, 36, 133-144.
-
-
-
-
29
-
-
0035852126
-
Palladium-catalyzed intramolecular C-O bond formation
-
Kuwabe, S.-I.; Torraca, K. E.; Buchwald, S. L. Palladium-catalyzed intramolecular C-O bond formation. J. Am. Chem. Soc. 2001, 123, 12202-12206.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 12202-12206
-
-
Kuwabe, S.-I.1
Torraca, K.E.2
Buchwald, S.L.3
-
30
-
-
36148947766
-
-
See Supporting Information for details
-
See Supporting Information for details.
-
-
-
-
31
-
-
0035100437
-
Cassette-accelerated rapid rat screen: A systematic procedure for the doing and liquid chromatography/atmospheric pressure ionization tandem mass spectrometric analysis of new chemical entities as part of new drug discovery
-
Korfmacher, W. A.; Cox, K. A.; Ng, K. J.; Veals, J.; Hsien, Y.; Wainhaus, S.; Broske, L.; Prelusky, D.; Nomeir, A.; White, R. E. Cassette-accelerated rapid rat screen: a systematic procedure for the doing and liquid chromatography/atmospheric pressure ionization tandem mass spectrometric analysis of new chemical entities as part of new drug discovery. Rapid Commun. Mass. Spectrom. 2001, 15, 335-340.
-
(2001)
Rapid Commun. Mass. Spectrom
, vol.15
, pp. 335-340
-
-
Korfmacher, W.A.1
Cox, K.A.2
Ng, K.J.3
Veals, J.4
Hsien, Y.5
Wainhaus, S.6
Broske, L.7
Prelusky, D.8
Nomeir, A.9
White, R.E.10
-
32
-
-
20944438126
-
-
Varty, G. B.; Grilli, M.; Forlani, A.; Fredduzzi, S.; Grzelak, M. E.; Guthrie, D. H.; Hodgson, R. A.; Sherry, X. L.; Nicolussi, E.; Pond, A. J.; Parker, E. M.; Hunter, J. C.; Higgins, G. A.; Reggiani, A.; Bertorelli, R. The antinociceptive and anxiolytic-like effects of the metabotropic glutamate receptor 5 (mGluR5) antagonists, MPEP and MTEP, and the mGluR1 antagonist, LY456236, in rodents: a comparison of efficacy and side-effect profiles. Psychopharmacology 2005, 179, 207-217. See also Supporting Information.
-
Varty, G. B.; Grilli, M.; Forlani, A.; Fredduzzi, S.; Grzelak, M. E.; Guthrie, D. H.; Hodgson, R. A.; Sherry, X. L.; Nicolussi, E.; Pond, A. J.; Parker, E. M.; Hunter, J. C.; Higgins, G. A.; Reggiani, A.; Bertorelli, R. The antinociceptive and anxiolytic-like effects of the metabotropic glutamate receptor 5 (mGluR5) antagonists, MPEP and MTEP, and the mGluR1 antagonist, LY456236, in rodents: a comparison of efficacy and side-effect profiles. Psychopharmacology 2005, 179, 207-217. See also Supporting Information.
-
-
-
|