-
1
-
-
23644440521
-
Metabotropic glutamate receptor 2 modulates excitatory synaptic transmission in the rat globus pallidus
-
DOI 10.1016/j.neuropharm.2005.03.006, PII S0028390805001061
-
Poisik, O.; Raju, D. V.; Verreault, M.; Rodriguez, A.; Abeniyi, O. A.; Conn, P. J.; Smith, Y. Metabotropic glutamate receptor 2 modulates excitatory synaptic transmission in the rat globus pallidus Neuropharmacology 2005, 49, 57-69 (Pubitemid 41115893)
-
(2005)
Neuropharmacology
, vol.49
, Issue.SUPPL.
, pp. 57-69
-
-
Poisik, O.1
Raju, D.V.2
Verreault, M.3
Rodriguez, A.4
Abeniyi, O.A.5
Conn, P.J.6
Smith, Y.7
-
2
-
-
33846177868
-
Metabotropic glutamate receptor targets for neuropsychiatric disorders
-
DOI 10.1016/j.ddstr.2006.10.018, PII S1740677306000842
-
Linden, A.-M.; Schoepp, D. D. Metabotropic glutamate receptor targets for neuropsychiatric disorders Drug Discovery Today: Ther. Strategies 2006, 3, 507-517 (Pubitemid 46076174)
-
(2006)
Drug Discovery Today: Therapeutic Strategies
, vol.3
, Issue.4
, pp. 507-517
-
-
Linden, A.-M.1
Schoepp, D.D.2
-
3
-
-
34948858402
-
Activation of mGlu2/3 receptors as a new approach to treat schizophrenia: A randomized Phase 2 clinical trial
-
DOI 10.1038/nm1632, PII NM1632
-
Patil, S. T.; Zhang, L.; Martenyi, F.; Lowe, S. L.; Jackson, K. A.; Andreev, B. V.; Avedisova, A. S.; Bardenstein, L. M.; Gurovich, I. Y.; Morozova, M. A.; Mosolov, S. N.; Neznanov, N. G.; Reznik, A. M.; Smulevich, A. B.; Tochilov, V. A.; Johnson, B. G.; Monn, J. A.; Schoepp, D. D. Activation of mGlu2/3 receptors as a new approach to treat schizophrenia: A randomized Phase 2 clinical trial Nature Med. 2007, 13, 1102-1107 (Pubitemid 47517511)
-
(2007)
Nature Medicine
, vol.13
, Issue.9
, pp. 1102-1107
-
-
Patil, S.T.1
Zhang, L.2
Martenyi, F.3
Lowe, S.L.4
Jackson, K.A.5
Andreev, B.V.6
Avedisova, A.S.7
Bardenstein, L.M.8
Gurovich, I.Y.9
Morozova, M.A.10
Mosolov, S.N.11
Neznanov, N.G.12
Reznik, A.M.13
Smulevich, A.B.14
Tochilov, V.A.15
Johnson, B.G.16
Monn, J.A.17
Schoepp, D.D.18
-
4
-
-
45749139623
-
Evidence for the role of metabotropic glutamate (mGlu)2 not mGlu3 receptors in the preclinical antipsychotic pharmacology of the mGlu2/3 receptor agonist (-)-(1R,4S,5S,6S)-4-amino-2-sulfonylbicyclo[3.1.0]hexane-4,6- dicarboxylic acid (LY404039)
-
DOI 10.1124/jpet.108.136861
-
Fell, M. J.; Svensson, K. A.; Johnson, B. G.; Schoepp, D. D. Evidence for the role of metabotropic glutamate (mGlu)2 not mGlu3 receptors in the preclinical antipsychotic pharmacology of the mGlu2/3 receptor agonist (-)-(1 R,4 S,5 S,6 S)-4-amino-2-sulfonylbicyclo[3.1.0]hexane-4,6-dicarboxylic acid (LY404039) J. Pharmacol. Exp. Ther. 2008, 326, 209-217 (Pubitemid 351872145)
-
(2008)
Journal of Pharmacology and Experimental Therapeutics
, vol.326
, Issue.1
, pp. 209-217
-
-
Fell, M.J.1
Svensson, K.A.2
Johnson, B.G.3
Schoepp, D.D.4
-
5
-
-
34249078595
-
Metabotropic glutamate receptors as drug targets
-
DOI 10.2174/138945007780618544
-
Recasens, M.; Guiramand, J.; Aimar, R.; Abdulkarium, A.; Barbanel, G. Metabotropic glutamate receptors as drug targets Curr. Drug Targets 2007, 8, 651-681 (Pubitemid 46785063)
-
(2007)
Current Drug Targets
, vol.8
, Issue.5
, pp. 651-681
-
-
Recasens, M.1
Guiramand, J.2
Aimar, R.3
Abdulkarim, A.4
Barbanel, G.5
-
7
-
-
69949125537
-
Positive allosteric modulators of the metabotropic glutamate receptor 2 for the treatment of schizophrenia
-
For recent reviews, see
-
For recent reviews, see Fraley, M. Positive allosteric modulators of the metabotropic glutamate receptor 2 for the treatment of schizophrenia Expert Opin. Ther. Pat. 2009, 19, 1259-1275
-
(2009)
Expert Opin. Ther. Pat.
, vol.19
, pp. 1259-1275
-
-
Fraley, M.1
-
8
-
-
35848941110
-
Allosteric modulators for mGlu receptors
-
DOI 10.2174/157015907781695900
-
Gasparini, F.; Spooren, W. Allosteric modulators for mGlu receptors Curr. Neuropharmacol. 2007, 5, 187-194 (Pubitemid 351863860)
-
(2007)
Current Neuropharmacology
, vol.5
, Issue.3
, pp. 187-194
-
-
Gasparini, F.1
Spooren, W.2
-
9
-
-
24644475202
-
Positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (mGluR2)
-
DOI 10.2174/1568026054750281
-
Rudd, M. T.; McCauley, J. A. Positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (mGluR2) Curr. Top. Med. Chem. 2005, 5, 869-884 For more recent publications, see the following: Tresadern, G.; Cid, J. M.; Macdonald, G. J.; Vega, J. A.; De Lucas, A. I.; Garcia, A.; Matesanz, E.; Linares, M. L.; Oehlrich, D.; Lavreysen, H.; Biesmans, I.; Trabanco, A. A. Scaffold hopping from pyridone to imidazo[1,2-a]puridines. New positive allosteric modulators of metabotropic glutamate 2 receptor Bioorg. Med. Chem. Lett. 2010, 20, 175-179 (Pubitemid 41282355)
-
(2005)
Current Topics in Medicinal Chemistry
, vol.5
, Issue.9
, pp. 869-884
-
-
Rudd, M.T.1
McCauley, J.A.2
-
10
-
-
77952100973
-
3-Aryl-5-phenoxymethyl-1,3-oxazolidin-2-ones as positive allosteric modulators of mGluR2 for the treatment of schizophrenia: Hit-to-lead efforts
-
Brnardic, E. J.; Fraley, M. E.; Garbaccio, R. M.; Layton, M. E.; Sanders, J. M.; Culberson, C.; Jacobson, M.; Magliaro, B. C.; Hutson, P. H.; O'Brien, J. A.; Huszar, S. L.; Uslander, J. M.; Fillgrove, K. L.; Tang, C.; Kuo, Y.; Sur, S. M.; Hartman, G. D. 3-Aryl-5-phenoxymethyl-1,3-oxazolidin-2-ones as positive allosteric modulators of mGluR2 for the treatment of schizophrenia: Hit-to-lead efforts Bioorg. Med. Chem. Lett. 2010, 20, 3129-3133
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 3129-3133
-
-
Brnardic, E.J.1
Fraley, M.E.2
Garbaccio, R.M.3
Layton, M.E.4
Sanders, J.M.5
Culberson, C.6
Jacobson, M.7
Magliaro, B.C.8
Hutson, P.H.9
O'Brien, J.A.10
Huszar, S.L.11
Uslander, J.M.12
Fillgrove, K.L.13
Tang, C.14
Kuo, Y.15
Sur, S.M.16
Hartman, G.D.17
-
11
-
-
78649291978
-
Discovery of oxazolobenzimidazoles as Postive Allosteric Modulators for the mGluR2 Receptor
-
Garbaccio, R. M.; Brnardict, E. J.; Fraley, M. E.; Hartman, G. D.; Hutson, P. H.; O'Brien, J. A.; Magliar, B. C.; Uslaner, J. M.; Huszar, S. L.; Fillgrove, K. L.; Small, J. H.; Tang, C.; Kuo, Y.; Jacobson, M. A. Discovery of oxazolobenzimidazoles as Postive Allosteric Modulators for the mGluR2 Receptor ACS Med. Chem. Lett. 2010, 1, 406-410
-
(2010)
ACS Med. Chem. Lett.
, vol.1
, pp. 406-410
-
-
Garbaccio, R.M.1
Brnardict, E.J.2
Fraley, M.E.3
Hartman, G.D.4
Hutson, P.H.5
O'Brien, J.A.6
Magliaro, B.C.7
Uslaner, J.M.8
Huszar, S.L.9
Fillgrove, K.L.10
Small, J.H.11
Tang, C.12
Kuo, Y.13
Jacobson, M.A.14
-
12
-
-
78650315615
-
Discovery of 1, 5-disubstituted pyridines: A new class of positive allosteric modulators of the metabotropic glutamate 2 receptor
-
Cid, J. M.; Duvey, G.; Cluzeau, P.; Nhem, V.; Macary, K.; Raux, A.; Poirier, N.; Muller, J.; Bolea, C; Finn, T.; Urios, I.; Epping-Jordan, M.; Chamelot, E.; Derouet, F.; Girard, F.; MacDonald, G. J.; Vega, J. A.; De Lucas, A. I.; Matesanz, E.; Lavreysen, H.; Linares, M. L.; Oehlrich, D.; Oyarzabal, H.; Tresadern, G.; Trabanco, A. A.; Andres, J. I.; Le Poul, E.; Imogai, H.; Lutjens, R.; Rocher, J.-P. Discovery of 1, 5-disubstituted pyridines: A new class of positive allosteric modulators of the metabotropic glutamate 2 receptor ACS Chem. Neurosci. 2010, 1, 788-795
-
(2010)
ACS Chem. Neurosci.
, vol.1
, pp. 788-795
-
-
Cid, J.M.1
Duvey, G.2
Cluzeau, P.3
Nhem, V.4
MacAry, K.5
Raux, A.6
Poirier, N.7
Muller, J.8
Bolea, C.9
Finn, T.10
Urios, I.11
Epping-Jordan, M.12
Chamelot, E.13
Derouet, F.14
Girard, F.15
MacDonald, G.J.16
Vega, J.A.17
De Lucas, A.I.18
Matesanz, E.19
Lavreysen, H.20
Linares, M.L.21
Oehlrich, D.22
Oyarzabal, H.23
Tresadern, G.24
Trabanco, A.A.25
Andres, J.I.26
Le Poul, E.27
Imogai, H.28
Lutjens, R.29
Rocher, J.-P.30
more..
-
13
-
-
53349165547
-
3-(Imidazolylmethyl)-3-aza-bicyclo[3.1.0]hexan-6-yl)methyl ethers: A novel series of mGluR2 positive allosteric modulators
-
Zhang, L.; Rogers, B. N.; Duplantier, A. J.; McHardy, S. F.; Efremov, I.; Berke, H.; Qian, W.; Zhang, A. Q.; Maklad, N.; Candler, J.; Doran, A. C.; Lazzaro, J. T., Jr.; Ganong, A. H. 3-(Imidazolylmethyl)-3-aza-bicyclo[3.1.0] hexan-6-yl)methyl ethers: A novel series of mGluR2 positive allosteric modulators Bioorg. Med. Chem. Lett. 2008, 18, 5493-5496
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5493-5496
-
-
Zhang, L.1
Rogers, B.N.2
Duplantier, A.J.3
McHardy, S.F.4
Efremov, I.5
Berke, H.6
Qian, W.7
Zhang, A.Q.8
Maklad, N.9
Candler, J.10
Doran, A.C.11
Lazzaro, Jr.J.T.12
Ganong, A.H.13
-
14
-
-
64249109525
-
3-Benzyl-1,3-oxazolidin-2-ones as mGluR2 positive allosteric modulators: Hit-to lead and lead optimization
-
Duplantier, A. J.; Efremov, I.; Candler, J.; Doran, A. C.; Ganong, A. H.; Haas, J. A.; Hanks, A. N.; Kraus, K. G.; Lazarro, J. T., Jr.; Lu, J.; Maklad, N.; McCarthy, S. A.; O'Sullivan, T. J.; Rogers, B. N.; Siuciak, J. A.; Spracklin, D. K.; Zhang, L. 3-Benzyl-1,3-oxazolidin-2-ones as mGluR2 positive allosteric modulators: Hit-to lead and lead optimization Bioorg. Med. Chem. Lett. 2009, 19, 2524-2529
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2524-2529
-
-
Duplantier, A.J.1
Efremov, I.2
Candler, J.3
Doran, A.C.4
Ganong, A.H.5
Haas, J.A.6
Hanks, A.N.7
Kraus, K.G.8
Lazarro, Jr.J.T.9
Lu, J.10
Maklad, N.11
McCarthy, S.A.12
O'Sullivan, T.J.13
Rogers, B.N.14
Siuciak, J.A.15
Spracklin, D.K.16
Zhang, L.17
-
15
-
-
72249115352
-
The identification of structurally novel, selective, orally bioavailable positive modulators of mGluR2
-
During the preparation of this manuscript, a structurally related series of mGluR2 PAMs was disclosed by D'Alessandro et al. For a reference, see
-
During the preparation of this manuscript, a structurally related series of mGluR2 PAMs was disclosed by D'Alessandro et al. For a reference, see D'Alessandro, P. L.; Corti, C.; Roth, A.; Ugolini, A.; Sava, A.; Montanari, D.; Bianchi, F.; Garland, S. L.; Powney, B.; Koppe, E. L.; Rocheville, M.; Osborne, G.; Perez, P.; De la Fuente, J.; De Los Frailes, M.; Smith, P. W.; Branch, C.; Nash, D.; Watson, S. P. The identification of structurally novel, selective, orally bioavailable positive modulators of mGluR2 Bioorg. Med. Chem. Lett. 2010, 20, 759-762
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 759-762
-
-
D'Alessandro, P.L.1
Corti, C.2
Roth, A.3
Ugolini, A.4
Sava, A.5
Montanari, D.6
Bianchi, F.7
Garland, S.L.8
Powney, B.9
Koppe, E.L.10
Rocheville, M.11
Osborne, G.12
Perez, P.13
De La Fuente, J.14
De Los Frailes, M.15
Smith, P.W.16
Branch, C.17
Nash, D.18
Watson, S.P.19
-
16
-
-
79952786161
-
-
20 glutamate challenge. Data are analyzed as a ratio of the peak fluorescence to the baseline after compound addition. Assay to assay variability in PAM potency required multiple experiments to determine potency, typically n > 3.
-
20 glutamate challenge. Data are analyzed as a ratio of the peak fluorescence to the baseline after compound addition. Assay to assay variability in PAM potency required multiple experiments to determine potency, typically n > 3.
-
-
-
-
17
-
-
44949250688
-
Blood-brain barrier permeability considerations for CNS-targeted compound library design
-
Hitchcock, S. A. Blood-brain barrier permeability considerations for CNS-targeted compound library design Curr. Opin. Chem. Biol. 2008, 12, 318-323
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 318-323
-
-
Hitchcock, S.A.1
-
18
-
-
35748934487
-
The influence of drug-like concepts on decision-making in medicinal chemistry
-
Leeson, P. D.; Springthorpe, B. The influence of drug-like concepts on decision-making in medicinal chemistry Nature Rev. Drug Discovery 2007, 6, 881-891
-
(2007)
Nature Rev. Drug Discovery
, vol.6
, pp. 881-891
-
-
Leeson, P.D.1
Springthorpe, B.2
-
19
-
-
79952785092
-
-
note
-
i = 426 nM). Compound 3 was also screened in mGluR1 (agonist, antagonist mode), mGluR5 (agonist, antagonist, PAM mode) functional assays with no activity detected up to 10 -M.
-
-
-
-
20
-
-
79952790518
-
-
note
-
2 receptors and measures the inhibition of quinpirole stimulation by the test compounds.
-
-
-
-
21
-
-
33746768115
-
Targeting the dopamine D2 receptor in schizophrenia
-
For a recent review, see
-
For a recent review, see Seeman, P. Targeting the dopamine D2 receptor in schizophrenia Expert Opin. Ther. Targets 2006, 10, 515-531
-
(2006)
Expert Opin. Ther. Targets
, vol.10
, pp. 515-531
-
-
Seeman, P.1
-
22
-
-
84986517183
-
Synthesis of the 1,2,3,4-tetrahydrobenzofuro[2,3-c]pyridine ring system
-
Jaen, J. C.; Wise, L. D. Synthesis of the 1,2,3,4-tetrahydrobenzofuro[2, 3-c]pyridine ring system J. Heterocycl. Chem. 1987, 24, 1317-1319
-
(1987)
J. Heterocycl. Chem.
, vol.24
, pp. 1317-1319
-
-
Jaen, J.C.1
Wise, L.D.2
-
23
-
-
79952791302
-
-
50 values > 3000 nM); compounds (+)- 17c - e were also screened in mGluR1 (agonist, antagonist mode), mGluR5 (agonist, antagonist, PAM mode) functional assays with no activity detected up to 10 -M.
-
50 values > 3000 nM); compounds (+)- 17c - e were also screened in mGluR1 (agonist, antagonist mode), mGluR5 (agonist, antagonist, PAM mode) functional assays with no activity detected up to 10 -M.
-
-
-
-
24
-
-
0033695199
-
Studies of Amphetamine or Methamphetamine Psychosis in Japan: Relation of Methamphetamine Psychosis to Schizophrenia
-
Yui, K.; Ikemoto, S.; Ishiguro, T.; Goto, K. Studies of Amphetamine or Methamphetamine Psychosis in Japan: Relation of Methamphetamine Psychosis to Schizophrenia Ann. N.Y. Acad. Sci. 2000, 914, 1-12
-
(2000)
Ann. N.Y. Acad. Sci.
, vol.914
, pp. 1-12
-
-
Yui, K.1
Ikemoto, S.2
Ishiguro, T.3
Goto, K.4
-
25
-
-
0346157993
-
Neuropharmacological Profile of an Atypical Antipsychotic, NRA0562
-
Hirota, S.; Kawashima, N.; Chaki, S.; Okuyama, S. Neuropharmacological Profile of an Atypical Antipsychotic, NRA0562 CNS Drug Rev. 2003, 9, 375-388 (Pubitemid 38031865)
-
(2003)
CNS Drug Reviews
, vol.9
, Issue.4
, pp. 375-388
-
-
Hirota, S.1
Kawashima, N.2
Chaki, S.3
Okuyama, S.4
-
26
-
-
48049095987
-
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 -methyl-3,6-dihydropyridine-1(2 H)-carboxamide
-
Satow, A.; Maehara, S.; Ise, S.; Hikichi, H.; Fukushima, M.; Suzuki, G.; Kimura, T.; Tanaka, T.; Ito, S.; Kawamoto, H.; Ohta, H. 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 -methyl-3,6- dihydropyridine-1(2 H)-carboxamide] J. Pharmacol. Exp. Ther. 2008, 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
Tanaka, T.8
Ito, S.9
Kawamoto, H.10
Ohta, H.11
-
27
-
-
0029956082
-
Synthesis and Pharmacological Characterization of All Sixteen Stereoisomers of 2-(2-Carboxy-3-phenylcyclopropyl)glycine. Focus on (2 S,1- S,2- S,3- R)-2-(2-Carboxy-3-phenylcyclopropyl)glycine, a Novel and Selective Group II Metabotropic Glutamate Receptor Antagonist
-
Marinozzi, M.; Natalini, B.; Constantino, G.; Tijskens, P.; Thomsen, C.; Pellicciari, R. Synthesis and Pharmacological Characterization of All Sixteen Stereoisomers of 2-(2-Carboxy-3-phenylcyclopropyl)glycine. Focus on (2 S,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
-
-
Marinozzi, M.1
Natalini, B.2
Constantino, G.3
Tijskens, P.4
Thomsen, C.5
Pellicciari, R.6
-
28
-
-
79952788728
-
Glutamate mGluR2/3 agonists inhibit mescaline-induced scratching in mice: A potential model of antipsychotic activity
-
abstract 1030.16.
-
Gross, G.; Wicke, K. M.; Mezler, M.; Schoemaker, H. Glutamate mGluR2/3 agonists inhibit mescaline-induced scratching in mice: A potential model of antipsychotic activity. 34th Annual Meeting of the Society for Neuroscience, 2004, abstract 1030.16.
-
(2004)
34th Annual Meeting of the Society for Neuroscience
-
-
Gross, G.1
Wicke, K.M.2
Mezler, M.3
Schoemaker, H.4
-
29
-
-
33846549510
-
2A Receptor-Mediated Signaling Pathways to Affect Behavior
-
DOI 10.1016/j.neuron.2007.01.008, PII S0896627307000281
-
Gonzalez-Maeso, J.; Weisstaub, N. V.; Zhou, M.; Chan, P.; Ivic, L.; Ang, R.; Lira, A; Bradley-Moore, M.; Ge, Y.; Zhou, Q.; Sealfon, S. C.; Gingrich, J. A. Hallucinogens recruit specific cortical 5-HT2A receptor-mediated signaling pathways to affect behavior Neuron 2007, 53, 439-452 (Pubitemid 46161267)
-
(2007)
Neuron
, vol.53
, Issue.3
, pp. 439-452
-
-
Gonzalez-Maeso, J.1
Weisstaub, N.V.2
Zhou, M.3
Chan, P.4
Ivic, L.5
Ang, R.6
Lira, A.7
Bradley-Moore, M.8
Ge, Y.9
Zhou, Q.10
Sealfon, S.C.11
Gingrich, J.A.12
-
30
-
-
0037630660
-
The hallucinogen 1-[2,5-dimethoxy-4-iodophenyl]-2-aminopropane (DOI) increases cortical extracellular glutamate levels in rats
-
DOI 10.1016/S0304-3940(03)00547-0
-
Scruggs, J. L.; Schmidt, D.; Deutch, A. Y. The hallucinogen 1-[2,5-dimethoxy-4-iodophenyl]-2-aminopropane (DOI) increases cortical extracellular glutamate levels in rats Neurosci. Lett. 2003, 346, 137-140 (Pubitemid 36829280)
-
(2003)
Neuroscience Letters
, vol.346
, Issue.3
, pp. 137-140
-
-
Scruggs, J.L.1
Schmidt, D.2
Deutch, A.Y.3
-
31
-
-
0034551757
-
DOI -induced activation of the cortex: Dependence on 5-HT2A heteroceptors on thalamocortical glutamatergic neurons
-
Scruggs, J. L.; Patel, S.; Bubser, M.; Deutch, A. Y. DOI -induced activation of the cortex: Dependence on 5-HT2A heteroceptors on thalamocortical glutamatergic neurons J. Neurosci. 2000, 20, 8846-8852
-
(2000)
J. Neurosci.
, vol.20
, pp. 8846-8852
-
-
Scruggs, J.L.1
Patel, S.2
Bubser, M.3
Deutch, A.Y.4
-
32
-
-
0033799996
-
A novel approach to the identification of psychiatric drugs: Serotonin-glutamate interactions in the prefrontal cortex
-
Marek, G. J. A novel approach to the identification of psychiatric drugs: Serotonin-glutamate interactions in the prefrontal cortex CNS Drug Rev. 2000, 6, 206-218
-
(2000)
CNS Drug Rev.
, vol.6
, pp. 206-218
-
-
Marek, G.J.1
-
33
-
-
0036874825
-
Influence of nonspecific brain and plasma binding on CNS exposure: Implications for rational drug discovery
-
DOI 10.1002/bdd.325
-
Kalvass, J. C.; Maurer, T. S. Influence of nonspecific brain and plasma binding on CNS exposure: Implications for rational drug discovery Biopharm. Drug Dispos. 2002, 23, 327-338 (Pubitemid 36124162)
-
(2002)
Biopharmaceutics and Drug Disposition
, vol.23
, Issue.8
, pp. 327-338
-
-
Kalvass, J.C.1
Maurer, T.S.2
|