메뉴 건너뛰기




Volumn 5, Issue 7, 2014, Pages 597-610

A novel class of succinimide-derived negative allosteric modulators of metabotropic glutamate receptor subtype 1 provides insight into a disconnect in activity between the rat and human receptors

Author keywords

Allosteric modulator; glutamate; metabotropic

Indexed keywords

5 [4 (HYDROXYEMTHYL)PIPERIDIN 1 YL] N (4 METHYLCYCLOHEXYL)PYRAZINE 2 CARBOXAMIDE; BAY 36 7620; LEUCINE; METABOTROPIC RECEPTOR 1; N CYCLOHEPTYLTHIENO[2,3 D]PYRIMIDIN 4 AMINE; R 214127; SUCCINIMIDE; SUCCINIMIDE DERIVATIVE; UNCLASSIFIED DRUG; VALINE; VU 0410425; AMINO ACID RECEPTOR AFFECTING AGENT; CALCIUM; METABOTROPIC GLUTAMATE RECEPTOR TYPE 1; METABOTROPIC RECEPTOR;

EID: 84904434885     PISSN: None     EISSN: 19487193     Source Type: Journal    
DOI: 10.1021/cn5000343     Document Type: Article
Times cited : (49)

References (50)
  • 1
    • 77949516412 scopus 로고    scopus 로고
    • Metabotropic glutamate receptors: Physiology, pharmacology, and disease
    • Niswender, C. M. and Conn, P. J. (2010) Metabotropic glutamate receptors: physiology, pharmacology, and disease Annu. Rev. Pharmacol. Toxicol. 50, 295-322
    • (2010) Annu. Rev. Pharmacol. Toxicol. , vol.50 , pp. 295-322
    • Niswender, C.M.1    Conn, P.J.2
  • 2
    • 80054741157 scopus 로고    scopus 로고
    • The role of group I mGlu receptors in the expression of ethanol-induced conditioned place preference and ethanol withdrawal seizures in rats
    • Kotlinska, J. H., Bochenski, M., and Danysz, W. (2011) The role of group I mGlu receptors in the expression of ethanol-induced conditioned place preference and ethanol withdrawal seizures in rats Eur. J. Pharmacol. 670, 154-161
    • (2011) Eur. J. Pharmacol. , vol.670 , pp. 154-161
    • Kotlinska, J.H.1    Bochenski, M.2    Danysz, W.3
  • 3
    • 72649085319 scopus 로고    scopus 로고
    • Effects of mGluR1 antagonism in the dorsal hippocampus on drug context-induced reinstatement of cocaine-seeking behavior in rats
    • Xie, X., Ramirez, D. R., Lasseter, H. C., and Fuchs, R. A. (2010) Effects of mGluR1 antagonism in the dorsal hippocampus on drug context-induced reinstatement of cocaine-seeking behavior in rats Psychopharmacology 208, 1-11
    • (2010) Psychopharmacology , vol.208 , pp. 1-11
    • Xie, X.1    Ramirez, D.R.2    Lasseter, H.C.3    Fuchs, R.A.4
  • 4
    • 33846292496 scopus 로고    scopus 로고
    • MGlu1 receptor blockade attenuates cue- and nicotine-induced reinstatement of extinguished nicotine self-administration behavior in rats
    • DOI 10.1016/j.neuropharm.2006.07.023, PII S0028390806002322
    • Dravolina, O. A., Zakharova, E. S., Shekunova, E. V., Zvartau, E. E., Danysz, W., and Bespalov, A. Y. (2007) mGlu1 receptor blockade attenuates cue- and nicotine-induced reinstatement of extinguished nicotine self-administration behavior in rats Neuropharmacology 52, 263-269 (Pubitemid 46123346)
    • (2007) Neuropharmacology , vol.52 , Issue.2 , pp. 263-269
    • Dravolina, O.A.1    Zakharova, E.S.2    Shekunova, E.V.3    Zvartau, E.E.4    Danysz, W.5    Bespalov, A.Y.6
  • 5
    • 48049095987 scopus 로고    scopus 로고
    • Pharmacological effects of the metabotropic glutamate receptor 1 antagonist compared with those of the metabotropic glutamate receptor 5 antagonist and metabotropic glutamate receptor 2/3 agonist in rodents
    • Detailed investigations with a selective allosteric metabotropic glutamate receptor 1 antagonist, FTIDC [4-[1-(2-fluoropyridine-3-yl)-5-methyl-1 H -1,2,3-triazol-4-yl]- N -isopropyl- N -methy l-3,6-dihydropyridine-1(2 H)-carboxamide]
    • Satow, A., Maehara, S., Ise, S., Hikichi, H., Fukushima, M., Suzuki, G., Kimura, T., Tanak, T., Ito, S., Kawamoto, H., and Ohta, H. (2008) Pharmacological effects of the metabotropic glutamate receptor 1 antagonist compared with those of the metabotropic glutamate receptor 5 antagonist and metabotropic glutamate receptor 2/3 agonist in rodents: detailed investigations with a selective allosteric metabotropic glutamate receptor 1 antagonist, FTIDC [4-[1-(2-fluoropyridine-3-yl)-5-methyl-1 H -1,2,3-triazol-4-yl]- N -isopropyl- N -methy l-3,6-dihydropyridine-1(2 H)-carboxamide] J. Pharmacol. Exp. Ther. 326, 577-586
    • (2008) J. Pharmacol. Exp. Ther. , vol.326 , pp. 577-586
    • Satow, A.1    Maehara, S.2    Ise, S.3    Hikichi, H.4    Fukushima, M.5    Suzuki, G.6    Kimura, T.7    Tanak, T.8    Ito, S.9    Kawamoto, H.10    Ohta, H.11
  • 6
    • 27744446102 scopus 로고    scopus 로고
    • Pharmacological characterization of stress-induced hyperthermia in DBA/2 mice using metabotropic and ionotropic glutamate receptor ligands
    • DOI 10.1007/s00213-005-0169-2
    • Rorick-Kehn, L. M., Hart, J. C., and McKinzie, D. L. (2005) Pharmacological characterization of stress-induced hyperthermia in DBA/2 mice using metabotropic and ionotropic glutamate receptor ligands Psychopharmacology 183, 226-240 (Pubitemid 41609275)
    • (2005) Psychopharmacology , vol.183 , Issue.2 , pp. 226-240
    • Rorick-Kehn, L.M.1    Hart, J.C.2    McKinzie, D.L.3
  • 8
    • 23644446890 scopus 로고    scopus 로고
    • Anticonvulsant effects of LY456236, a selective mGlu1 receptor antagonist
    • DOI 10.1016/j.neuropharm.2005.05.010, PII S0028390805001942
    • Shannon, H. E., Peters, S. C., and Kingston, A. E. (2005) Anticonvulsant effects of LY456236, a selective mGlu1 receptor antagonist Neuropharmacology 49 (Suppl 1) 188-195 (Pubitemid 41115905)
    • (2005) Neuropharmacology , vol.49 , Issue.SUPPL. , pp. 188-195
    • Shannon, H.E.1    Peters, S.C.2    Kingston, A.E.3
  • 9
    • 0141755379 scopus 로고    scopus 로고
    • Comparison of the effect of glutamate receptor modulators in the 6 Hz and maximal electroshock seizure models
    • DOI 10.1016/j.eplepsyres.2003.08.001
    • Barton, M. E., Peters, S. C., and Shannon, H. E. (2003) Comparison of the effect of glutamate receptor modulators in the 6 Hz and maximal electroshock seizure models Epilepsy Res. 56, 17-26 (Pubitemid 37177052)
    • (2003) Epilepsy Research , vol.56 , Issue.1 , pp. 17-26
    • Barton, M.E.1    Peters, S.C.2    Shannon, H.E.3
  • 13
    • 67649993985 scopus 로고    scopus 로고
    • Unique antipsychotic activities of the selective metabotropic glutamate receptor 1 allosteric antagonist 2-cyclopropyl-5-[1-(2-fluoro-3-pyridinyl)-5- methyl-1 H -1,2,3-triazol-4-yl]-2,3-dihydro-1 H -isoindol-1-one
    • Satow, A., Suzuki, G., Maehara, S., Hikichi, H., Murai, T., Kawagoe-Takaki, H., Hata, M., Ito, S., Ozaki, S., Kawamoto, H., and Ohta, H. (2009) Unique antipsychotic activities of the selective metabotropic glutamate receptor 1 allosteric antagonist 2-cyclopropyl-5-[1-(2-fluoro-3-pyridinyl)-5- methyl-1 H -1,2,3-triazol-4-yl]-2,3-dihydro-1 H -isoindol-1-one J. Pharmacol. Exp. Ther. 330, 179-190
    • (2009) J. Pharmacol. Exp. Ther. , vol.330 , pp. 179-190
    • Satow, A.1    Suzuki, G.2    Maehara, S.3    Hikichi, H.4    Murai, T.5    Kawagoe-Takaki, H.6    Hata, M.7    Ito, S.8    Ozaki, S.9    Kawamoto, H.10    Ohta, H.11
  • 14
    • 77953622543 scopus 로고    scopus 로고
    • Pharmacological effects of metabotropic glutamate receptor ligands on prepulse inhibition in DBA/2J mice
    • Hikichi, H., Nishino, M., Fukushima, M., Satow, A., Maehara, S., Kawamoto, H., and Ohta, H. (2010) Pharmacological effects of metabotropic glutamate receptor ligands on prepulse inhibition in DBA/2J mice Eur. J. Pharmacol. 639, 99-105
    • (2010) Eur. J. Pharmacol. , vol.639 , pp. 99-105
    • Hikichi, H.1    Nishino, M.2    Fukushima, M.3    Satow, A.4    Maehara, S.5    Kawamoto, H.6    Ohta, H.7
  • 15
    • 68949136974 scopus 로고    scopus 로고
    • Discovery and in vitro and in vivo profiles of 4-fluoro- N -[4-[6-(isopropylamino)pyrimidin-4-yl]-1,3-thiazol-2-yl]- N -methylbenzamide as novel class of an orally active metabotropic glutamate receptor 1 (mGluR1) antagonist
    • Satoh, A., Nagatomi, Y., Hirata, Y., Ito, S., Suzuki, G., Kimura, T., Maehara, S., Hikichi, H., Satow, A., Hata, M., Ohta, H., and Kawamoto, H. (2009) Discovery and in vitro and in vivo profiles of 4-fluoro- N -[4-[6- (isopropylamino)pyrimidin-4-yl]-1,3-thiazol-2-yl]- N -methylbenzamide as novel class of an orally active metabotropic glutamate receptor 1 (mGluR1) antagonist Bioorg. Med. Chem. Lett. 19, 5464-5468
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 5464-5468
    • Satoh, A.1    Nagatomi, Y.2    Hirata, Y.3    Ito, S.4    Suzuki, G.5    Kimura, T.6    Maehara, S.7    Hikichi, H.8    Satow, A.9    Hata, M.10    Ohta, H.11    Kawamoto, H.12
  • 16
    • 68949107534 scopus 로고    scopus 로고
    • Discovery and biological profile of isoindolinone derivatives as novel metabotropic glutamate receptor 1 antagonists: A potential treatment for psychotic disorders
    • Ito, S., Hirata, Y., Nagatomi, Y., Satoh, A., Suzuki, G., Kimura, T., Satow, A., Maehara, S., Hikichi, H., Hata, M., Ohta, H., and Kawamoto, H. (2009) Discovery and biological profile of isoindolinone derivatives as novel metabotropic glutamate receptor 1 antagonists: a potential treatment for psychotic disorders Bioorg. Med. Chem. Lett. 19, 5310-5313
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 5310-5313
    • Ito, S.1    Hirata, Y.2    Nagatomi, Y.3    Satoh, A.4    Suzuki, G.5    Kimura, T.6    Satow, A.7    Maehara, S.8    Hikichi, H.9    Hata, M.10    Ohta, H.11    Kawamoto, H.12
  • 17
    • 1442275398 scopus 로고    scopus 로고
    • 3H]R214127
    • DOI 10.1016/j.neuropharm.2003.11.014, PII S002839080300443X
    • Lavreysen, H., Pereira, S. N., Leysen, J. E., Langlois, X., and Lesage, A. S. (2004) Metabotropic glutamate 1 receptor distribution and occupancy in the rat brain: a quantitative autoradiographic study using [3H]R214127 Neuropharmacology 46, 609-619 (Pubitemid 38292965)
    • (2004) Neuropharmacology , vol.46 , Issue.5 , pp. 609-619
    • Lavreysen, H.1    Pereira, S.N.2    Leysen, J.E.3    Langlois, X.4    Lesage, A.S.J.5
  • 18
    • 0037731410 scopus 로고    scopus 로고
    • 3H]R214127: A novel high-affinity radioligand for the mGlu1 receptor reveals a common binding site shared by multiple allosteric antagonists
    • DOI 10.1124/mol.63.5.1082
    • Lavreysen, H., Janssen, C., Bischoff, F., Langlois, X., Leysen, J. E., and Lesage, A. S. (2003) [3H]R214127: a novel high-affinity radioligand for the mGlu1 receptor reveals a common binding site shared by multiple allosteric antagonists Mol. Pharmacol. 63, 1082-1093 (Pubitemid 36529927)
    • (2003) Molecular Pharmacology , vol.63 , Issue.5 , pp. 1082-1093
    • Lavreysen, H.1    Janssen, C.2    Bischoff, F.3    Langlois, X.4    Leysen, J.E.5    Lesage, A.S.J.6
  • 23
    • 33947213963 scopus 로고    scopus 로고
    • Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma
    • DOI 10.1158/0008-5472.CAN-06-3665
    • Namkoong, J., Shin, S. S., Lee, H. J., Marin, Y. E., Wall, B. A., Goydos, J. S., and Chen, S. (2007) Metabotropic glutamate receptor 1 and glutamate signaling in human melanoma Cancer Res. 67, 2298-2305 (Pubitemid 46424250)
    • (2007) Cancer Research , vol.67 , Issue.5 , pp. 2298-2305
    • Namkoong, J.1    Shin, S.-S.2    Hwa, J.L.3    Marin, Y.E.4    Wall, B.A.5    Goydos, J.S.6    Chen, S.7
  • 24
    • 84859107394 scopus 로고    scopus 로고
    • Metabotropic glutamate receptor-1: A potential therapeutic target for the treatment of breast cancer
    • Speyer, C. L., Smith, J. S., Banda, M., DeVries, J. A., Mekani, T., and Gorski, D. H. (2012) Metabotropic glutamate receptor-1: a potential therapeutic target for the treatment of breast cancer Breast Cancer Res. Treat. 132, 565-573
    • (2012) Breast Cancer Res. Treat. , vol.132 , pp. 565-573
    • Speyer, C.L.1    Smith, J.S.2    Banda, M.3    Devries, J.A.4    Mekani, T.5    Gorski, D.H.6
  • 25
    • 67649992440 scopus 로고    scopus 로고
    • Recent progress in the discovery and development of negative allosteric modulators of mGluR5
    • Lindsley, C. W. and Emmitte, K. A. (2009) Recent progress in the discovery and development of negative allosteric modulators of mGluR5 Curr. Opin. Drug Discovery Dev. 12, 446-457
    • (2009) Curr. Opin. Drug Discovery Dev. , vol.12 , pp. 446-457
    • Lindsley, C.W.1    Emmitte, K.A.2
  • 29
    • 80455173693 scopus 로고    scopus 로고
    • Discovery, synthesis, and structure-activity relationship development of a series of N -4-(2,5-dioxopyrrolidin-1-yl)phenylpicolinamides (VU0400195, ML182): Characterization of a novel positive allosteric modulator of the metabotropic glutamate receptor 4 (mGlu(4)) with oral efficacy in an antiparkinsonian animal model
    • Jones, C. K., Engers, D. W., Thompson, A. D., Field, J. R., Blobaum, A. L., Lindsley, S. R., Zhou, Y., Gogliotti, R. D., Jadhav, S., Zamorano, R., Bogenpohl, J., Smith, Y., Morrison, R., Daniels, J. S., Weaver, C. D., Conn, P. J., Lindsley, C. W., Niswender, C. M., and Hopkins, C. R. (2011) Discovery, synthesis, and structure-activity relationship development of a series of N -4-(2,5-dioxopyrrolidin-1-yl)phenylpicolinamides (VU0400195, ML182): characterization of a novel positive allosteric modulator of the metabotropic glutamate receptor 4 (mGlu(4)) with oral efficacy in an antiparkinsonian animal model J. Med. Chem. 54, 7639-7647
    • (2011) J. Med. Chem. , vol.54 , pp. 7639-7647
    • Jones, C.K.1    Engers, D.W.2    Thompson, A.D.3    Field, J.R.4    Blobaum, A.L.5    Lindsley, S.R.6    Zhou, Y.7    Gogliotti, R.D.8    Jadhav, S.9    Zamorano, R.10    Bogenpohl, J.11    Smith, Y.12    Morrison, R.13    Daniels, J.S.14    Weaver, C.D.15    Conn, P.J.16    Lindsley, C.W.17    Niswender, C.M.18    Hopkins, C.R.19
  • 33
    • 27844482134 scopus 로고    scopus 로고
    • A close structural analog of 2-methyl-6-(phenylethynyl)-pyridine acts as a neutral allosteric site ligand on metabotropic glutamate receptor subtype 5 and blocks the effects of multiple allosteric modulators
    • DOI 10.1124/mol.105.016139
    • Rodriguez, A. L., Nong, Y., Sekaran, N. K., Alagille, D., Tamagnan, G. D., and Conn, P. J. (2005) A close structural analog of 2-methyl-6- (phenylethynyl)-pyridine acts as a neutral allosteric site ligand on metabotropic glutamate receptor subtype 5 and blocks the effects of multiple allosteric modulators Mol. Pharmacol. 68, 1793-1802 (Pubitemid 41654362)
    • (2005) Molecular Pharmacology , vol.68 , Issue.6 , pp. 1793-1802
    • Rodriguez, A.L.1    Nong, Y.2    Sekaran, N.K.3    Alagille, D.4    Tamagnan, G.D.5    Conn, P.J.6
  • 34
    • 47149106805 scopus 로고    scopus 로고
    • Synthesis and SAR of a mGluR5 allosteric partial antagonist lead: Unexpected modulation of pharmacology with slight structural modifications to a 5-(phenylethynyl)pyrimidine scaffold
    • Sharma, S., Rodriguez, A. L., Conn, P. J., and Lindsley, C. W. (2008) Synthesis and SAR of a mGluR5 allosteric partial antagonist lead: unexpected modulation of pharmacology with slight structural modifications to a 5-(phenylethynyl)pyrimidine scaffold Bioorg. Med. Chem. Lett. 18, 4098-4101
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 4098-4101
    • Sharma, S.1    Rodriguez, A.L.2    Conn, P.J.3    Lindsley, C.W.4
  • 36
    • 33746265808 scopus 로고    scopus 로고
    • A novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators
    • DOI 10.1124/mol.105.021857
    • Hemstapat, K., de Paulis, T., Chen, Y., Brady, A. E., Grover, V. K., Alagille, D., Tamagnan, G. D., and Conn, P. J. (2006) A novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators Mol. Pharmacol. 70, 616-626 (Pubitemid 44092322)
    • (2006) Molecular Pharmacology , vol.70 , Issue.2 , pp. 616-626
    • Hemstapat, K.1    De Paulis, T.2    Chen, Y.3    Brady, A.E.4    Grover, V.K.5    Alagille, D.6    Tamagnan, G.D.7    Conn, P.J.8
  • 39
    • 34248667888 scopus 로고    scopus 로고
    • Pharmacological characterization of a new, orally active and potent allosteric metabotropic glutamate receptor 1 antagonist, 4-[1-(2-fluoropyridin- 3-yl)-5-methyl-1H-1,2,3-triazol-4-yl]-N-isopropyl-N-methyl-3, 6-dihydropyridine-1(2H)-carboxamide (FTIDC)
    • DOI 10.1124/jpet.106.116574
    • Suzuki, G., Kimura, T., Satow, A., Kaneko, N., Fukuda, J., Hikichi, H., Sakai, N., Maehara, S., Kawagoe-Takaki, H., Hata, M., Azuma, T., Ito, S., Kawamoto, H., and Ohta, H. (2007) Pharmacological characterization of a new, orally active and potent allosteric metabotropic glutamate receptor 1 antagonist, 4-[1-(2-fluoropyridin-3-yl)-5-methyl-1 H -1,2,3-triazol-4-yl]- N -isopropyl- N -methyl-3,6-dihydropyridine-1(2 H)-carboxamide (FTIDC) J. Pharmacol. Exp. Ther. 321, 1144-1153 (Pubitemid 46766521)
    • (2007) Journal of Pharmacology and Experimental Therapeutics , vol.321 , Issue.3 , pp. 1144-1153
    • Suzuki, G.1    Kimura, T.2    Satow, A.3    Kaneko, N.4    Fukuda, J.5    Hikichi, H.6    Sakai, N.7    Maehara, S.8    Kawagoe-Takaki, H.9    Hata, M.10    Azuma, T.11    Ito, S.12    Kawamoto, H.13    Ohta, H.14
  • 40
    • 79955556415 scopus 로고    scopus 로고
    • Radiosynthesis and preliminary evaluation of 4-[18F]fluoro- N -[4-[6-(isopropylamino)pyrimidin-4-yl]-1,3-thiazol-2-yl]- N -methylbenzamide as a new positron emission tomography ligand for metabotropic glutamate receptor subtype 1
    • Yamasaki, T., Fujinaga, M., Yoshida, Y., Kumata, K., Yui, J., Kawamura, K., Hatori, A., Fukumura, T., and Zhang, M. R. (2011) Radiosynthesis and preliminary evaluation of 4-[18F]fluoro- N -[4-[6-(isopropylamino)pyrimidin-4- yl]-1,3-thiazol-2-yl]- N -methylbenzamide as a new positron emission tomography ligand for metabotropic glutamate receptor subtype 1 Bioorg. Med. Chem. Lett. 21, 2998-3001
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 2998-3001
    • Yamasaki, T.1    Fujinaga, M.2    Yoshida, Y.3    Kumata, K.4    Yui, J.5    Kawamura, K.6    Hatori, A.7    Fukumura, T.8    Zhang, M.R.9
  • 41
    • 20944438126 scopus 로고    scopus 로고
    • 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
    • DOI 10.1007/s00213-005-2143-4
    • Varty, G. B., Grilli, M., Forlani, A., Fredduzzi, S., Grzelak, M. E., Guthrie, D. H., Hodgson, R. A., Lu, S. X., Nicolussi, E., Pond, A. J., Parker, E. M., Hunter, J. C., Higgins, G. A., Reggiani, A., and Bertorelli, R. (2005) 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 179, 207-217 (Pubitemid 40576708)
    • (2005) Psychopharmacology , vol.179 , Issue.1 , pp. 207-217
    • Varty, G.B.1    Grilli, M.2    Forlani, A.3    Fredduzzi, S.4    Grzelak, M.E.5    Guthrie, D.H.6    Hodgson, R.A.7    Lu, S.X.8    Nicolussi, E.9    Pond, A.J.10    Parker, E.M.11    Hunter, J.C.12    Higgins, G.A.13    Reggiani, A.14    Bertorelli, R.15
  • 42
    • 20144369074 scopus 로고    scopus 로고
    • Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGlu1 antagonists
    • DOI 10.1021/jm049499o
    • Mabire, D., Coupa, S., Adelinet, C., Poncelet, A., Simonnet, Y., Venet, M., Wouters, R., Lesage, A. S., Van Beijsterveldt, L., and Bischoff, F. (2005) Synthesis, structure-activity relationship, and receptor pharmacology of a new series of quinoline derivatives acting as selective, noncompetitive mGlu1 antagonists J. Med. Chem. 48, 2134-2153 (Pubitemid 40396342)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.6 , pp. 2134-2153
    • Mabire, D.1    Coupa, S.2    Adelinet, C.3    Poncelet, A.4    Simonnet, Y.5    Venet, M.6    Wouters, R.7    Lesage, A.S.J.8    Van Beijsterveldt, L.9    Bischoff, F.10
  • 45
    • 0037424518 scopus 로고    scopus 로고
    • Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glutamate 1 receptor
    • DOI 10.1074/jbc.M211759200
    • Malherbe, P., Kratochwil, N., Knoflach, F., Zenner, M. T., Kew, J. N., Kratzeisen, C., Maerki, H. P., Adam, G., and Mutel, V. (2003) Mutational analysis and molecular modeling of the allosteric binding site of a novel, selective, noncompetitive antagonist of the metabotropic glutamate 1 receptor J. Biol. Chem. 278, 8340-8347 (Pubitemid 36800582)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.10 , pp. 8340-8347
    • Malherbe, P.1    Kratochwil, N.2    Knoflach, F.3    Zenner, M.-T.4    Kew, J.N.C.5    Kratzeisen, C.6    Maerki, H.P.7    Adam, G.8    Mutel, V.9
  • 46
    • 34447632041 scopus 로고    scopus 로고
    • Allosteric GPCR modulators: Taking advantage of permissive receptor pharmacology
    • DOI 10.1016/j.tips.2007.06.004, PII S0165614707001496, Allosterism and Collateral Efficacy
    • Leach, K., Sexton, P. M., and Christopoulos, A. (2007) Allosteric GPCR modulators: taking advantage of permissive receptor pharmacology Trends Pharmacol. Sci. 28, 382-389 (Pubitemid 47087967)
    • (2007) Trends in Pharmacological Sciences , vol.28 , Issue.8 , pp. 382-389
    • Leach, K.1    Sexton, P.M.2    Christopoulos, A.3
  • 48
    • 72449206576 scopus 로고    scopus 로고
    • Efficient synthesis of 1,4-diaryl-5-methyl-1,2,3-triazole, a potential mGluR1 antagonist, and the risk assessment study of arylazides
    • Tsuritani, T., Mizuno, H., Nonoyama, N., Kii, S., Akao, A., Sato, K., Yasuda, N., and Mase, T. (2009) Efficient synthesis of 1,4-diaryl-5-methyl-1,2, 3-triazole, a potential mGluR1 antagonist, and the risk assessment study of arylazides Org. Process Res. Dev. 13, 1407-1412
    • (2009) Org. Process Res. Dev. , vol.13 , pp. 1407-1412
    • Tsuritani, T.1    Mizuno, H.2    Nonoyama, N.3    Kii, S.4    Akao, A.5    Sato, K.6    Yasuda, N.7    Mase, T.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.