-
1
-
-
0036780743
-
G-Protein-Coupled Receptor Oligomerization and Its Potential for Drug Discovery
-
George S. R., O'Dowd B. F., Lee S. P., G-Protein-Coupled Receptor Oligomerization and Its Potential for Drug Discovery. Nat. Rev. Drug Discov. 2002, 1, 808-820.
-
(2002)
Nat. Rev. Drug Discov
, vol.1
, pp. 808-820
-
-
George, S.R.1
O'Dowd, B.F.2
Lee, S.P.3
-
2
-
-
0035040530
-
Genetic Variations and Polymorphisms of G Protein-Coupled Receptors: Functional and Therapeutic Implications
-
Rana B. K., Shiina T., Insel P. A., Genetic Variations and Polymorphisms of G Protein-Coupled Receptors: Functional and Therapeutic Implications. Annu. Rev. Pharmacol. Toxicol. 2001, 41, 593-624.
-
(2001)
Annu. Rev. Pharmacol. Toxicol
, vol.41
, pp. 593-624
-
-
Rana, B.K.1
Shiina, T.2
Insel, P.A.3
-
3
-
-
0035283073
-
Orphan G-Protein-Coupled Receptors and Natural Ligand Discovery
-
Howard A. D., McAllister G., Feighner S. D.,. Orphan G-Protein-Coupled Receptors and Natural Ligand Discovery. Trends Pharmacol. Sci. 2001, 22, 132-140.
-
(2001)
Trends Pharmacol. Sci
, vol.22
, pp. 132-140
-
-
Howard, A.D.1
McAllister, G.2
Feighner, S.D.3
-
4
-
-
58149193205
-
Allosteric Modulators of GPCRs: A Novel Approach for the Treatment of CNS Disorders
-
Jeffrey Conn P., Christopoulos A., Lindsley C. W., Allosteric Modulators of GPCRs: A Novel Approach for the Treatment of CNS Disorders. Nat. Rev. Drug Discov. 2009, 8, 41-54.
-
(2009)
Nat. Rev. Drug Discov
, vol.8
, pp. 41-54
-
-
Jeffrey Conn, P.1
Christopoulos, A.2
Lindsley, C.W.3
-
5
-
-
58149119377
-
Activation of Metabotropic Glutamate Receptors as a Novel Approach for the Treatment of Schizophrenia
-
Conn P. J., Lindsley C. W., Jones C. K., Activation of Metabotropic Glutamate Receptors as a Novel Approach for the Treatment of Schizophrenia. Trends Pharmacol. Sci. 2009, 30, 25-31.
-
(2009)
Trends Pharmacol. Sci
, vol.30
, pp. 25-31
-
-
Conn, P.J.1
Lindsley, C.W.2
Jones, C.K.3
-
6
-
-
33749440087
-
Muscarinic Acetylcholine Receptors
-
Ishii M., Kurachi Y., Muscarinic Acetylcholine Receptors. Curr. Pharmaceut. Des. 2006, 12, 3573-3581.
-
(2006)
Curr. Pharmaceut. des
, vol.12
, pp. 3573-3581
-
-
Ishii, M.1
Kurachi, Y.2
-
7
-
-
38349193123
-
Muscarinic Acetylcholine Receptors as CNS Drug Targets
-
Langmead C. J., Watson J., Reavill C., Muscarinic Acetylcholine Receptors as CNS Drug Targets. Pharmacol. Ther. 2008, 117, 232-243.
-
(2008)
Pharmacol. Ther
, vol.117
, pp. 232-243
-
-
Langmead, C.J.1
Watson, J.2
Reavill, C.3
-
8
-
-
18344398824
-
Anticholinergics for Symptomatic Management of Parkinson's Disease
-
3, CD003735
-
Katzenschlager R., Sampaio C., Costa J., Lees A., Anticholinergics for Symptomatic Management of Parkinson's Disease. Cochrane Database Sys. Rev. 2002, 3, CD003735.
-
(2002)
Cochrane Database Sys. Rev
-
-
Katzenschlager, R.1
Sampaio, C.2
Costa, J.3
Lees, A.4
-
9
-
-
84905223141
-
Discovery, Synthesis and Characterization of a Highly Muscarinic Acetylcholine Receptor (mAChR)-Selective M5-Orthosteric Antagonist, VU0488130 (ML381): A Novel Molecular Probe
-
Gentry P. R., Kokubo M., Bridges T. M.,. Discovery, Synthesis and Characterization of a Highly Muscarinic Acetylcholine Receptor (mAChR)-Selective M5-Orthosteric Antagonist, VU0488130 (ML381): A Novel Molecular Probe. ChemMedChem. 2014, 9, 1677-1682.
-
(2014)
ChemMedChem
, vol.9
, pp. 1677-1682
-
-
Gentry, P.R.1
Kokubo, M.2
Bridges, T.M.3
-
10
-
-
23844517718
-
Quantifying Bioactivity on a Large Scale: Quality Assurance and Analysis of Multiparametric Ultra-HTS Data
-
Heyse S., Bruttger O., Duerr O.,. Quantifying Bioactivity on a Large Scale: Quality Assurance and Analysis of Multiparametric Ultra-HTS Data. J. La. Automat. 2005, 10, 207-212.
-
(2005)
J. La. Automat
, vol.10
, pp. 207-212
-
-
Heyse, S.1
Bruttger, O.2
Duerr, O.3
-
11
-
-
84855961051
-
Discovery of a Highly Selective in Vitro and in Vivo M4 Positive Allosteric Modulator (PAM)
-
In; National Center for Biotechnology Information, Bethesda, MD
-
Lewis L. M., Bridges T. M., Niswender C. M.,. Discovery of a Highly Selective In Vitro and In Vivo M4 Positive Allosteric Modulator (PAM). In Probe Reports from the NIH Molecular Libraries Program; National Center for Biotechnology Information, Bethesda, MD, 2010.
-
(2010)
Probe Reports from the NIH Molecular Libraries Program
-
-
Lewis, L.M.1
Bridges, T.M.2
Niswender, C.M.3
-
12
-
-
0027245830
-
Substitution of Three Amino Acids Switches Receptor Specificity of Gq Alpha to That of Gi Alpha
-
Conklin B. R., Farfel Z., Lustig K. D.,. Substitution of Three Amino Acids Switches Receptor Specificity of Gq Alpha to That of Gi Alpha. Nature 1993, 363, 274-276.
-
(1993)
Nature
, vol.363
, pp. 274-276
-
-
Conklin, B.R.1
Farfel, Z.2
Lustig, K.D.3
-
13
-
-
0033003760
-
A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays
-
Zhang J. H., Chung T., Oldenburg K., A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays. J. Biomol. Screen. 1999, 4, 67-73.
-
(1999)
J. Biomol. Screen
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.2
Oldenburg, K.3
-
14
-
-
84904624070
-
Identification of Potent and Selective Inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PfM18AAP) of Human Malaria via High-Throughput Screening
-
Spicer T., Fernandez-Vega V., Chase P.,. Identification of Potent and Selective Inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PfM18AAP) of Human Malaria via High-Throughput Screening. J. Biomol. Screen. 2014, 19, 1107-1115.
-
(2014)
J. Biomol. Screen
, vol.19
, pp. 1107-1115
-
-
Spicer, T.1
Fernandez-Vega, V.2
Chase, P.3
-
15
-
-
84908866820
-
Identification of Selective Agonists and Positive Allosteric Modulators for Micro- and Delta-Opioid Receptors from a Single High-Throughput Screen
-
Burford N. T., Wehrman T., Bassoni D.,. Identification of Selective Agonists and Positive Allosteric Modulators for Micro- and Delta-Opioid Receptors from a Single High-Throughput Screen. J. Biomol. Screen. 2014, 19, 1255-1265.
-
(2014)
J. Biomol. Screen
, vol.19
, pp. 1255-1265
-
-
Burford, N.T.1
Wehrman, T.2
Bassoni, D.3
-
16
-
-
77954482106
-
A Multiplex Calcium Assay for Identification of GPCR Agonists and Antagonists
-
Liu K., Southall N., Titus S.,. A Multiplex Calcium Assay for Identification of GPCR Agonists and Antagonists. Assay Drug Dev. Technol. 2010, 8, 367-369.
-
(2010)
Assay Drug Dev. Technol
, vol.8
, pp. 367-369
-
-
Liu, K.1
Southall, N.2
Titus, S.3
-
17
-
-
33748671369
-
The 7 TM G-Protein-Coupled Receptor Target Family
-
Jacoby E., Bouhelal R., Gerspacher M.,. The 7 TM G-Protein-Coupled Receptor Target Family. ChemMedChem. 2006, 1, 761-782.
-
(2006)
ChemMedChem
, vol.1
, pp. 761-782
-
-
Jacoby, E.1
Bouhelal, R.2
Gerspacher, M.3
-
18
-
-
78649919580
-
Discovery of Novel Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 Reveals Chemical and Functional Diversity and in Vivo Activity in Rat Behavioral Models of Anxiolytic and Antipsychotic Activity
-
Rodriguez A. L., Grier M. D., Jones C. K.,. Discovery of Novel Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 Reveals Chemical and Functional Diversity and In Vivo Activity in Rat Behavioral Models of Anxiolytic and Antipsychotic Activity. Mol. Pharmacol. 2010, 78, 1105-1123.
-
(2010)
Mol. Pharmacol
, vol.78
, pp. 1105-1123
-
-
Rodriguez, A.L.1
Grier, M.D.2
Jones, C.K.3
-
19
-
-
84867246771
-
Development of a High-Throughput Calcium Flux Assay for Identification of All Ligand Types Including Positive, Negative, and Silent Allosteric Modulators for G Protein-Coupled Receptors
-
Noblin D. J., Bertekap R. L. Jr., Burford N. T.,. Development of a High-Throughput Calcium Flux Assay for Identification of All Ligand Types Including Positive, Negative, and Silent Allosteric Modulators for G Protein-Coupled Receptors. Assay Drug Dev. Technol. 2012, 10, 457-467.
-
(2012)
Assay Drug Dev. Technol
, vol.10
, pp. 457-467
-
-
Noblin, D.J.1
Bertekap, R.L.2
Burford, N.T.3
-
20
-
-
73549095525
-
Selective and Brain Penetrant Neuropeptide y y2 Receptor Antagonists Discovered by Whole-Cell High-Throughput Screening
-
Brothers S. P., Saldanha S. A., Spicer T. P.,. Selective and Brain Penetrant Neuropeptide y y2 Receptor Antagonists Discovered by Whole-Cell High-Throughput Screening. Mol. Pharmacol. 2010, 77, 46-57.
-
(2010)
Mol. Pharmacol
, vol.77
, pp. 46-57
-
-
Brothers, S.P.1
Saldanha, S.A.2
Spicer, T.P.3
-
21
-
-
0037442769
-
Identification of Metabotropic Glutamate Receptor Antagonists Using an Automated High-Throughput Screening System
-
Hodder P., Cassaday J., Peltier R.,. Identification of Metabotropic Glutamate Receptor Antagonists Using an Automated High-Throughput Screening System. Anal. Biochem. 2003, 313, 246-254.
-
(2003)
Anal. Biochem
, vol.313
, pp. 246-254
-
-
Hodder, P.1
Cassaday, J.2
Peltier, R.3
-
22
-
-
84862964996
-
Functional Impact of Allosteric Agonist Activity of Selective Positive Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 in Regulating Central Nervous System Function
-
Noetzel M. J., Rook J. M., Vinson P. N.,. Functional Impact of Allosteric Agonist Activity of Selective Positive Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 5 in Regulating Central Nervous System Function. Mol. Pharmacol. 2012, 81, 120-133.
-
(2012)
Mol. Pharmacol
, vol.81
, pp. 120-133
-
-
Noetzel, M.J.1
Rook, J.M.2
Vinson, P.N.3
-
23
-
-
61349093537
-
Subtype-Selective Allosteric Modulators of Muscarinic Receptors for the Treatment of CNS Disorders
-
Conn P. J., Jones C. K., Lindsley C. W., Subtype-Selective Allosteric Modulators of Muscarinic Receptors for the Treatment of CNS Disorders. Trends Pharmacol. Sci. 2009, 30, 148-155.
-
(2009)
Trends Pharmacol. Sci
, vol.30
, pp. 148-155
-
-
Conn, P.J.1
Jones, C.K.2
Lindsley, C.W.3
-
24
-
-
84949116313
-
Discovery and SAR of Muscarinic Receptor Subtype 1 (M) Allosteric Activators from a Molecular Libraries High Throughput Screen. Part 1: 2,5-Dibenzyl-2H-pyrazolo[4,3-c]quinolin-3(5H)-ones as Positive Allosteric Modulators
-
Han C., Chatterjee A., Noetzel M. J.,. Discovery and SAR of Muscarinic Receptor Subtype 1 (M) Allosteric Activators from a Molecular Libraries High Throughput Screen. Part 1: 2,5-Dibenzyl-2H-pyrazolo[4,3-c]quinolin-3(5H)-ones as Positive Allosteric Modulators. Bioorg. Med. Chem. Lett. 2015, 25, 384-388.
-
(2015)
Bioorg. Med. Chem. Lett
, vol.25
, pp. 384-388
-
-
Han, C.1
Chatterjee, A.2
Noetzel, M.J.3
-
25
-
-
41149111966
-
A Novel Assay of Gi/o-Linked G Protein-Coupled Receptor Coupling to Potassium Channels Provides New Insights into the Pharmacology of the Group III Metabotropic Glutamate Receptors
-
Niswender C. M., Johnson K. A., Luo Q.,. A Novel Assay of Gi/o-Linked G Protein-Coupled Receptor Coupling to Potassium Channels Provides New Insights into the Pharmacology of the Group III Metabotropic Glutamate Receptors. Mol. Pharmacol. 2008, 73, 1213-1224.
-
(2008)
Mol. Pharmacol
, vol.73
, pp. 1213-1224
-
-
Niswender, C.M.1
Johnson, K.A.2
Luo, Q.3
-
27
-
-
79955479052
-
Discovery and Optimization of a Novel, Selective and Brain Penetrant M1 Positive Allosteric Modulator (PAM): The Development of ML169, an MLPCN Probe
-
Reid P. R., Bridges T. M., Sheffler D. J.,. Discovery and Optimization of a Novel, Selective and Brain Penetrant M1 Positive Allosteric Modulator (PAM): The Development of ML169, an MLPCN Probe. Bioorg. Med. Chem. Lett. 2011, 21, 2697-2701.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 2697-2701
-
-
Reid, P.R.1
Bridges, T.M.2
Sheffler, D.J.3
-
28
-
-
84905223141
-
Discovery, Synthesis and Characterization of a Highly Muscarinic Acetylcholine Receptor (mAChR)-Selective M5-Orthosteric Antagonist, VU0488130 (ML381): A Novel Molecular Probe
-
Gentry P. R., Kokubo M., Bridges T. M.,. Discovery, Synthesis and Characterization of a Highly Muscarinic Acetylcholine Receptor (mAChR)-Selective M5-Orthosteric Antagonist, VU0488130 (ML381): A Novel Molecular Probe. ChemMedChem. 2014, 9, 1677-1682.
-
(2014)
ChemMedChem
, vol.9
, pp. 1677-1682
-
-
Gentry, P.R.1
Kokubo, M.2
Bridges, T.M.3
|