-
1
-
-
27744589455
-
Muscarinic receptor subtype pharmacology and physiology
-
Eglen, R. M. Muscarinic receptor subtype pharmacology and physiology Prog. Med. Chem. 2005, 43, 105-136
-
(2005)
Prog. Med. Chem.
, vol.43
, pp. 105-136
-
-
Eglen, R.M.1
-
2
-
-
34548362105
-
Muscarinic acetylcholine receptors: Mutant mice provide new insights for drug development
-
Wess, J.; Eglen, R. M.; Gautam, D. Muscarinic acetylcholine receptors: mutant mice provide new insights for drug development Nat. Rev. Drug Discovery 2007, 6, 721-733
-
(2007)
Nat. Rev. Drug Discovery
, vol.6
, pp. 721-733
-
-
Wess, J.1
Eglen, R.M.2
Gautam, D.3
-
3
-
-
77954612317
-
Allosteric activators of muscarinic receptors as novel approaches for treatment of CNS disorders
-
Digby, G. J.; Shirey, J. K.; Conn, P. J. Allosteric activators of muscarinic receptors as novel approaches for treatment of CNS disorders Mol. BioSyst. 2010, 6, 1345-1354
-
(2010)
Mol. BioSyst.
, vol.6
, pp. 1345-1354
-
-
Digby, G.J.1
Shirey, J.K.2
Conn, P.J.3
-
4
-
-
19944401545
-
Allosterism at muscarinic receptors: Ligands and mechanisms
-
Birdsall, N. J. M.; Lazareno, S. Allosterism at muscarinic receptors: ligands and mechanisms Mini-Rev. Med. Chem. 2005, 33, 523-543
-
(2005)
Mini-Rev. Med. Chem.
, vol.33
, pp. 523-543
-
-
Birdsall, N.J.M.1
Lazareno, S.2
-
5
-
-
77951985712
-
Allosteric ligands for G protein-coupled receptors: A novel strategy with attractive therapeutic opportunities
-
De Amici, M.; Dallanoce, C.; Holzgrabe, U.; Tränkle, C.; Mohr, K. Allosteric ligands for G protein-coupled receptors: a novel strategy with attractive therapeutic opportunities Med. Res. Rev. 2010, 30, 463-549
-
(2010)
Med. Res. Rev.
, vol.30
, pp. 463-549
-
-
De Amici, M.1
Dallanoce, C.2
Holzgrabe, U.3
Tränkle, C.4
Mohr, K.5
-
6
-
-
33847122495
-
Allosteric modulation of G protein-coupled receptors
-
May, L. T.; Leach, K.; Sexton, P. M.; Christopoulos, A. Allosteric modulation of G protein-coupled receptors Annu. Rev. Pharmacol. Toxicol. 2007, 47, 14.1-14.51
-
(2007)
Annu. Rev. Pharmacol. Toxicol.
, vol.47
, pp. 141-1451
-
-
May, L.T.1
Leach, K.2
Sexton, P.M.3
Christopoulos, A.4
-
7
-
-
34347395367
-
A novel, conformation-specific allosteric inhibitor of the tachykinin NK2 receptor (NK2R) with functionally selective properties
-
Maillet, E. L.; Pellegrini, N.; Valant, C.; Bucher, B.; Hibert, M.; Bourguignon, J.-J.; Galzi, J.-L. A novel, conformation-specific allosteric inhibitor of the tachykinin NK2 receptor (NK2R) with functionally selective properties FASEB J. 2007, 21, 2124-2134
-
(2007)
FASEB J.
, vol.21
, pp. 2124-2134
-
-
Maillet, E.L.1
Pellegrini, N.2
Valant, C.3
Bucher, B.4
Hibert, M.5
Bourguignon, J.-J.6
Galzi, J.-L.7
-
8
-
-
0023958554
-
Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods
-
Ehlert, F. J. Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods Mol. Pharmacol. 1988, 35, 187-194
-
(1988)
Mol. Pharmacol.
, vol.35
, pp. 187-194
-
-
Ehlert, F.J.1
-
9
-
-
10744223983
-
N -Desmethylclozapine, an allosteric agonist at muscarinic M1 receptor, potentiates N -methyl- d -aspartate receptor activity
-
Sur, C.; Mallorga, P. J.; Wittmann, M.; Jacobson, M. A.; Pascarella, D.; Williams, J. B.; Brandish, P. E.; Pettibone, D. J.; Scolnick, E. M.; Conn, P. J. N -Desmethylclozapine, an allosteric agonist at muscarinic M1 receptor, potentiates N -methyl- d -aspartate receptor activity Proc. Natl. Acad. Sci. U.S.A. 2003, 100, 13674-13679
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 13674-13679
-
-
Sur, C.1
Mallorga, P.J.2
Wittmann, M.3
Jacobson, M.A.4
Pascarella, D.5
Williams, J.B.6
Brandish, P.E.7
Pettibone, D.J.8
Scolnick, E.M.9
Conn, P.J.10
-
10
-
-
0036259109
-
Discovery of an ectopic activation site on the M1 muscarinic receptor
-
Spalding, T. A.; Trotter, C.; Skjaerbaek, N.; Messier, T. L.; Currier, E. A.; Burstein, E. S.; Li, D.; Hacksell, U.; Brann, M. R. Discovery of an ectopic activation site on the M1 muscarinic receptor Mol. Pharmacol. 2002, 61, 1297-1302
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 1297-1302
-
-
Spalding, T.A.1
Trotter, C.2
Skjaerbaek, N.3
Messier, T.L.4
Currier, E.A.5
Burstein, E.S.6
Li, D.7
Hacksell, U.8
Brann, M.R.9
-
11
-
-
30044435787
-
Probing the molecular mechanism of interaction between 4- n -butyl-1-[4-(2-methylphenyl)-4-oxo-1-butyl]-piperidine (AC-42) and the muscarinic M1 receptor: Direct pharmacological evidence that AC-42 is an allosteric agonist
-
Langmead, C. J.; Fry, V. A. H.; Forbes, I. T.; Branch, C. L.; Christopoulos, A.; Wood, M. D.; Herdon, H. J. Probing the molecular mechanism of interaction between 4- n -butyl-1-[4-(2-methylphenyl)-4-oxo-1-butyl]-piperidine (AC-42) and the muscarinic M1 receptor: direct pharmacological evidence that AC-42 is an allosteric agonist Mol. Pharmacol. 2006, 69, 236-246
-
(2006)
Mol. Pharmacol.
, vol.69
, pp. 236-246
-
-
Langmead, C.J.1
Fry, V.A.H.2
Forbes, I.T.3
Branch, C.L.4
Christopoulos, A.5
Wood, M.D.6
Herdon, H.J.7
-
12
-
-
33751072945
-
Structural requirements of transmembrane domain 3 for activation by the M1 muscarinic receptor agonists AC-42, AC-260584, clozapine, and N -desmethylclozapine: Evidence for three distinct modes of receptor activation
-
Spalding, T. A.; Ma, J. N.; Ott, T. R.; Friberg, M.; Bajpai, A.; Risso Bradley, S.; Davis, R. E.; Brann, M. R.; Burstein, E. S. Structural requirements of transmembrane domain 3 for activation by the M1 muscarinic receptor agonists AC-42, AC-260584, clozapine, and N -desmethylclozapine: evidence for three distinct modes of receptor activation Mol. Pharmacol. 2006, 70, 1974-1983
-
(2006)
Mol. Pharmacol.
, vol.70
, pp. 1974-1983
-
-
Spalding, T.A.1
Ma, J.N.2
Ott, T.R.3
Friberg, M.4
Bajpai, A.5
Risso Bradley, S.6
Davis, R.E.7
Brann, M.R.8
Burstein, E.S.9
-
13
-
-
46249084634
-
Characterization of a CNS penetrant, selective M1 muscarinic receptor agonist, 77-LH-28-1
-
Langmead, C. J.; Austin, N. E.; Branch, C. L.; Brown, J. T.; Buchanan, K. A.; Davies, C. H.; Forbes, I. T.; Fry, V. A. H.; Hagan, J. J.; Herdon, H. J.; Jones, G. A.; Jeggo, R.; Kew, J. N. C.; Mazzali, A.; Melarange, R. Characterization of a CNS penetrant, selective M1 muscarinic receptor agonist, 77-LH-28-1 Br. J. Pharmacol. 2008, 154, 1104-1115
-
(2008)
Br. J. Pharmacol.
, vol.154
, pp. 1104-1115
-
-
Langmead, C.J.1
Austin, N.E.2
Branch, C.L.3
Brown, J.T.4
Buchanan, K.A.5
Davies, C.H.6
Forbes, I.T.7
Fry, V.A.H.8
Hagan, J.J.9
Herdon, H.J.10
Jones, G.A.11
Jeggo, R.12
Kew, J.N.C.13
Mazzali, A.14
Melarange, R.15
-
14
-
-
55249118679
-
Novel selective allosteric activator of the M1 muscarinic acetylcholine receptor regulates amyloid processing and produces antipsychotic-like activity in rats
-
Jones, C. K.; Brady, A. E.; Davis, A. A.; Xiang, Z.; Bubser, M.; Tantawy, M. N.; Kane, A. S.; Bridges, T. M.; Kennedy, J. P.; Bradley, S. R.; Peterson, T. E.; Ansari, M. S.; Baldwin, R. M. Novel selective allosteric activator of the M1 muscarinic acetylcholine receptor regulates amyloid processing and produces antipsychotic-like activity in rats J. Neurosci. 2008, 28, 10422-10433
-
(2008)
J. Neurosci.
, vol.28
, pp. 10422-10433
-
-
Jones, C.K.1
Brady, A.E.2
Davis, A.A.3
Xiang, Z.4
Bubser, M.5
Tantawy, M.N.6
Kane, A.S.7
Bridges, T.M.8
Kennedy, J.P.9
Bradley, S.R.10
Peterson, T.E.11
Ansari, M.S.12
Baldwin, R.M.13
-
15
-
-
77956318161
-
Discovery of N -{1-[3-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)propyl] piperidin-4-yl}-2-phenylacetamide (Lu AE51090): An allosteric muscarinic M1 receptor agonist with unprecedented selectivity and precognitive potential
-
Sams, A. G.; Hentzer, M.; Mikkelsen, G. K.; Larsen, K.; Bundgaard, C.; Plath, N.; Christofferson, C. T.; Bang-Andersen, B. Discovery of N -{1-[3-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)propyl]piperidin-4-yl} -2-phenylacetamide (Lu AE51090): an allosteric muscarinic M1 receptor agonist with unprecedented selectivity and precognitive potential J. Med. Chem. 2010, 53, 6386-6397
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6386-6397
-
-
Sams, A.G.1
Hentzer, M.2
Mikkelsen, G.K.3
Larsen, K.4
Bundgaard, C.5
Plath, N.6
Christofferson, C.T.7
Bang-Andersen, B.8
-
16
-
-
77952947252
-
Discovery and characterization of novel subtype-selective allosteric agonists for the investigation of M1 receptor function in the central nervous system
-
Lebois, E. P.; Bridges, T. M.; Lewis, L. M.; Dawson, E. S.; Kane, A. S.; Xiang, Z.; Jadhav, S.; Yin, H.; Kennedy, J. P.; Meiler, J.; Niswender, C. M.; Jones, C. K.; Conn, P. J.; Weaver, C. D.; Lindsley, C. W. Discovery and characterization of novel subtype-selective allosteric agonists for the investigation of M1 receptor function in the central nervous system ACS Chem. Neurosci. 2010, 1, 104-121
-
(2010)
ACS Chem. Neurosci.
, vol.1
, pp. 104-121
-
-
Lebois, E.P.1
Bridges, T.M.2
Lewis, L.M.3
Dawson, E.S.4
Kane, A.S.5
Xiang, Z.6
Jadhav, S.7
Yin, H.8
Kennedy, J.P.9
Meiler, J.10
Niswender, C.M.11
Jones, C.K.12
Conn, P.J.13
Weaver, C.D.14
Lindsley, C.W.15
-
17
-
-
72049088792
-
AC-260584, an orally bioavailable M1 muscarinic receptor allosteric agonist, improves cognitive performance in an animal model
-
Bradley, S. R.; Lameh, J.; Ohrmund, L.; Son, T.; Bajpai, A.; Nguyen, D.; Friberg, M.; Burstein, E. S.; Spalding, T. A.; Ott, T. R.; Schiffer, H. H.; Tabatabaei, A.; McFarland, K.; Davis, R. E.; Bonhaus, D. W. AC-260584, an orally bioavailable M1 muscarinic receptor allosteric agonist, improves cognitive performance in an animal model Neuropharmacology 2010, 58, 365-373
-
(2010)
Neuropharmacology
, vol.58
, pp. 365-373
-
-
Bradley, S.R.1
Lameh, J.2
Ohrmund, L.3
Son, T.4
Bajpai, A.5
Nguyen, D.6
Friberg, M.7
Burstein, E.S.8
Spalding, T.A.9
Ott, T.R.10
Schiffer, H.H.11
Tabatabaei, A.12
McFarland, K.13
Davis, R.E.14
Bonhaus, D.W.15
-
18
-
-
78649946419
-
Facilitation of long-term potentiation by muscarinic M1 receptors is mediated by inhibition of SK channels
-
Buchanan, K. A.; Petrovic, M. M.; Chamberlain, S. E. L.; Marrion, N. V.; Mellor, J. R. Facilitation of long-term potentiation by muscarinic M1 receptors is mediated by inhibition of SK channels Neuron 2010, 68, 948-963
-
(2010)
Neuron
, vol.68
, pp. 948-963
-
-
Buchanan, K.A.1
Petrovic, M.M.2
Chamberlain, S.E.L.3
Marrion, N.V.4
Mellor, J.R.5
-
19
-
-
54349106685
-
G protein coupling and signalling pathway activation by M1 muscarinic acetylcholine receptor orthosteric and allosteric agonists
-
Thomas, R. L.; Mistry, R.; Langmead, C. J.; Wood, M. D.; Challiss, R. A. J. G protein coupling and signalling pathway activation by M1 muscarinic acetylcholine receptor orthosteric and allosteric agonists J. Pharmacol. Exp. Ther. 2008, 327, 365-374
-
(2008)
J. Pharmacol. Exp. Ther.
, vol.327
, pp. 365-374
-
-
Thomas, R.L.1
Mistry, R.2
Langmead, C.J.3
Wood, M.D.4
Challiss, R.A.J.5
-
20
-
-
73349107462
-
Contrasting effects of allosteric and orthosteric agonists on M1 muscarinic acetylcholine receptor internalization and down-regulation
-
Thomas, R. L.; Langmead, C. J.; Wood, M. D.; Challiss, R. A. J. Contrasting effects of allosteric and orthosteric agonists on M1 muscarinic acetylcholine receptor internalization and down-regulation J. Pharmacol. Exp. Ther. 2009, 331, 1086-1095
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.331
, pp. 1086-1095
-
-
Thomas, R.L.1
Langmead, C.J.2
Wood, M.D.3
Challiss, R.A.J.4
-
21
-
-
77955887321
-
Differential effects of allosteric M1 muscarinic acetylcholine receptor agonists on receptor activation, arrestin 3 recruitment, and receptor downregulation
-
Davis, A. A.; Heilman, C. J.; Brady, A. E.; Miller, N. R.; Fuerstenau-Sharp, M.; Hanson, B. J.; Lindsley, C. W.; Conn, P. J.; Lah, J. J.; Levey, A. I. Differential effects of allosteric M1 muscarinic acetylcholine receptor agonists on receptor activation, arrestin 3 recruitment, and receptor downregulation ACS Chem. Neurosci. 2010, 1, 542-551
-
(2010)
ACS Chem. Neurosci.
, vol.1
, pp. 542-551
-
-
Davis, A.A.1
Heilman, C.J.2
Brady, A.E.3
Miller, N.R.4
Fuerstenau-Sharp, M.5
Hanson, B.J.6
Lindsley, C.W.7
Conn, P.J.8
Lah, J.J.9
Levey, A.I.10
-
22
-
-
77957055780
-
Integrated methods for the construction of three dimensional models and computational probing of structure-function relationships in G-protein coupled receptors
-
Ballesteros, J. A.; Weinstein, H. Integrated methods for the construction of three dimensional models and computational probing of structure-function relationships in G-protein coupled receptors Methods Neurosci. 1995, 25, 366-428
-
(1995)
Methods Neurosci.
, vol.25
, pp. 366-428
-
-
Ballesteros, J.A.1
Weinstein, H.2
-
23
-
-
59449090754
-
Mutagenic mapping suggests a novel binding mode for selective agonists of M1 muscarinic acetylcholine receptors
-
Lebon, G.; Langmead, C. J.; Tehan, B. G.; Hulme, E. C. Mutagenic mapping suggests a novel binding mode for selective agonists of M1 muscarinic acetylcholine receptors Mol. Pharmacol. 2009, 75, 331-341
-
(2009)
Mol. Pharmacol.
, vol.75
, pp. 331-341
-
-
Lebon, G.1
Langmead, C.J.2
Tehan, B.G.3
Hulme, E.C.4
-
24
-
-
77953777461
-
Orthosteric and allosteric modes of interaction of novel selective agonists of the M1 muscarinic acetylcholine receptor
-
Avlani, V. A.; Langmead, C. J.; Guida, E.; Wood, M. D.; Tehan, B. G.; Herdon, H. J.; Watson, J. M.; Sexton, P. M.; Christopoulos, A. Orthosteric and allosteric modes of interaction of novel selective agonists of the M1 muscarinic acetylcholine receptor Mol. Pharmacol. 2010, 78, 94-104
-
(2010)
Mol. Pharmacol.
, vol.78
, pp. 94-104
-
-
Avlani, V.A.1
Langmead, C.J.2
Guida, E.3
Wood, M.D.4
Tehan, B.G.5
Herdon, H.J.6
Watson, J.M.7
Sexton, P.M.8
Christopoulos, A.9
-
25
-
-
77951223981
-
Identification of orthosteric and allosteric site mutations in M2 muscarinic acetylcholine receptors that contribute to ligand-selective signalling bias
-
Gregory, K. J.; Hall, N. E.; Tobin, A. B.; Sexton, P. M.; Christopoulos, A. Identification of orthosteric and allosteric site mutations in M2 muscarinic acetylcholine receptors that contribute to ligand-selective signalling bias J. Biol. Chem. 2010, 285, 7459-7474
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 7459-7474
-
-
Gregory, K.J.1
Hall, N.E.2
Tobin, A.B.3
Sexton, P.M.4
Christopoulos, A.5
-
26
-
-
77957233070
-
The M1 muscarinic receptor allosteric agonists AC-42 and 1-[1′-(2-methylbenzyl)-1,4′-bipiperidin-4-yl]-1,3-dihydro-2 H -benzimidazol-2-one bind to a unique site distinct from the acetylcholine orthosteric site
-
Jacobson, M. A.; Kreatsoulas, C.; Pascarella, D. M.; O'Brien, J. A.; Sur, C. The M1 muscarinic receptor allosteric agonists AC-42 and 1-[1′-(2-methylbenzyl)-1,4′-bipiperidin-4-yl]-1,3-dihydro-2 H -benzimidazol-2-one bind to a unique site distinct from the acetylcholine orthosteric site Mol. Pharmacol. 2010, 78, 648-657
-
(2010)
Mol. Pharmacol.
, vol.78
, pp. 648-657
-
-
Jacobson, M.A.1
Kreatsoulas, C.2
Pascarella, D.M.3
O'Brien, J.A.4
Sur, C.5
-
27
-
-
0038334965
-
Fluorescence resonance energy transfer to probe human M1 muscarinic receptor structure and drug binding properties
-
Ilien, B.; Franchet, C.; Bernard, P.; Morisset, S.; Weill, C. O.; Bourguignon, J.-J.; Hibert, M.; Galzi, J.-L. Fluorescence resonance energy transfer to probe human M1 muscarinic receptor structure and drug binding properties J. Neurochem. 2003, 85, 768-778
-
(2003)
J. Neurochem.
, vol.85
, pp. 768-778
-
-
Ilien, B.1
Franchet, C.2
Bernard, P.3
Morisset, S.4
Weill, C.O.5
Bourguignon, J.-J.6
Hibert, M.7
Galzi, J.-L.8
-
28
-
-
67749116459
-
Pirenzepine promotes the dimerization of muscarinic M1 receptors through a three-step binding process
-
Ilien, B.; Glasser, N.; Clamme, J.-P.; Didier, P.; Piemont, E.; Chinnappan, R.; Daval, S. B.; Galzi, J.-L.; Mely, Y. Pirenzepine promotes the dimerization of muscarinic M1 receptors through a three-step binding process J. Biol. Chem. 2009, 284, 19533-19543
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 19533-19543
-
-
Ilien, B.1
Glasser, N.2
Clamme, J.-P.3
Didier, P.4
Piemont, E.5
Chinnappan, R.6
Daval, S.B.7
Galzi, J.-L.8
Mely, Y.9
-
29
-
-
44649157592
-
Antipsychotic-like behavioural effects and cognitive enhancement by a potent and selective muscarinic M1 receptor agonist, AC-260584
-
Vanover, K. E.; Veinbergs, I.; Davis, R. E. Antipsychotic-like behavioural effects and cognitive enhancement by a potent and selective muscarinic M1 receptor agonist, AC-260584 Behav. Neurosci. 2008, 122, 570-575
-
(2008)
Behav. Neurosci.
, vol.122
, pp. 570-575
-
-
Vanover, K.E.1
Veinbergs, I.2
Davis, R.E.3
-
30
-
-
15144345928
-
Selective endothelin A receptor antagonists: Discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivatives
-
Astles, P. C.; Brealey, C.; Brown, T. J.; Facchini, V.; Handscombe, C.; Harris, N. V.; McCarthy, C.; McLay, I. M.; Porter, B.; Roach, A. G.; Sargent, C.; Smith, C.; Walsh, R. J. A. Selective endothelin A receptor antagonists: discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivatives J. Med. Chem. 1998, 41, 2732-2744
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2732-2744
-
-
Astles, P.C.1
Brealey, C.2
Brown, T.J.3
Facchini, V.4
Handscombe, C.5
Harris, N.V.6
McCarthy, C.7
McLay, I.M.8
Porter, B.9
Roach, A.G.10
Sargent, C.11
Smith, C.12
Walsh, R.J.A.13
-
31
-
-
0042666435
-
Carbonyl participation in the solvolysis of ketone derivatives. The observation and isolation of intermediates
-
Ward, H. R.; Sherman, P. D. Carbonyl participation in the solvolysis of ketone derivatives. The observation and isolation of intermediates J. Am. Chem. Soc. 1968, 90, 3812-3817
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 3812-3817
-
-
Ward, H.R.1
Sherman, P.D.2
-
32
-
-
0026080085
-
Coupling of arylboronic acids with a partially reduced pyridine derivative
-
Wustrow, D. J.; Wise, L. D. Coupling of arylboronic acids with a partially reduced pyridine derivative Synthesis 1991, 11, 993-995
-
(1991)
Synthesis
, vol.11
, pp. 993-995
-
-
Wustrow, D.J.1
Wise, L.D.2
-
33
-
-
0000202518
-
Palladium-catalyzed olefination of vinyl triflates
-
Scott, W. J.; Pena, M. R.; Sward, K.; Stoessel, S. J.; Stille, J. K. Palladium-catalyzed olefination of vinyl triflates J. Org. Chem. 1985, 50, 2302-2308
-
(1985)
J. Org. Chem.
, vol.50
, pp. 2302-2308
-
-
Scott, W.J.1
Pena, M.R.2
Sward, K.3
Stoessel, S.J.4
Stille, J.K.5
-
34
-
-
0030834998
-
Elaboration of the side-chain of amino acid derivatives by palladium catalysed couplings
-
Crisp, G. T.; Jiang, Y.-L.; Pullman, P. J.; De Savi, C. Elaboration of the side-chain of amino acid derivatives by palladium catalysed couplings Tetrahedron 1997, 53, 17489-17500
-
(1997)
Tetrahedron
, vol.53
, pp. 17489-17500
-
-
Crisp, G.T.1
Jiang, Y.-L.2
Pullman, P.J.3
De Savi, C.4
-
35
-
-
0032487893
-
N -Boc ethyl oxamate: A new nitrogen nucleophile for use in Mitsunobu reactions
-
Berrée, F.; Michelot, G.; Le Corre, M. N -Boc ethyl oxamate: a new nitrogen nucleophile for use in Mitsunobu reactions Tetrahedron Lett. 1998, 39, 8275-8276
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8275-8276
-
-
Berrée, F.1
Michelot, G.2
Le Corre, M.3
-
36
-
-
53849112953
-
Solid-phase organic tagging resins for labeling biomolecules by 1,3-dipolar cycloaddition: Application to the synthesis of a fluorescent non-peptidic vasopressin receptor ligand
-
Bonnet, D.; Riche, S.; Loison, S.; Dagher, R.; Frantz, M. C.; Boudier, L.; Rahmeh, R.; Mouillac, B.; Haiech, J.; Hibert, M. Solid-phase organic tagging resins for labeling biomolecules by 1,3-dipolar cycloaddition: application to the synthesis of a fluorescent non-peptidic vasopressin receptor ligand Chem.-Eur. J. 2008, 14, 6247-6254
-
(2008)
Chem.-Eur. J.
, vol.14
, pp. 6247-6254
-
-
Bonnet, D.1
Riche, S.2
Loison, S.3
Dagher, R.4
Frantz, M.C.5
Boudier, L.6
Rahmeh, R.7
Mouillac, B.8
Haiech, J.9
Hibert, M.10
-
37
-
-
0035077936
-
Chemistry of sulforhodamine-amine conjugates
-
Corrie, J. E. T.; Davis, C. T.; Eccleston, J. F. Chemistry of sulforhodamine-amine conjugates Bioconjugate Chem. 2001, 12, 186-194
-
(2001)
Bioconjugate Chem.
, vol.12
, pp. 186-194
-
-
Corrie, J.E.T.1
Davis, C.T.2
Eccleston, J.F.3
-
38
-
-
3843100563
-
Fluorescent pirenzepine derivatives as potential bitopic ligands of the human M1 muscarinic receptor
-
Tahtaoui, C.; Parrot, I.; Klotz, P.; Guillier, F.; Galzi, J.-L.; Hibert, M.; Ilien, B. Fluorescent pirenzepine derivatives as potential bitopic ligands of the human M1 muscarinic receptor J. Med. Chem. 2004, 47, 4300-4315
-
(2004)
J. Med. Chem.
, vol.47
, pp. 4300-4315
-
-
Tahtaoui, C.1
Parrot, I.2
Klotz, P.3
Guillier, F.4
Galzi, J.-L.5
Hibert, M.6
Ilien, B.7
-
39
-
-
0032770310
-
Functional characterization and potential applications for enhanced green fluorescent protein- and epitope-fused human M1 muscarinic receptors
-
Weill, C.; Galzi, J. L.; Chasserot-Golaz, S.; Goeldner, M.; Ilien, B. Functional characterization and potential applications for enhanced green fluorescent protein- and epitope-fused human M1 muscarinic receptors J. Neurochem. 1999, 73, 791-801
-
(1999)
J. Neurochem.
, vol.73
, pp. 791-801
-
-
Weill, C.1
Galzi, J.L.2
Chasserot-Golaz, S.3
Goeldner, M.4
Ilien, B.5
-
40
-
-
0029126526
-
Detection, quantitation, and verification of allosteric interactions of agents with labeled and unlabeled ligands at G protein-coupled receptors: Interactions of strychnine and acetylcholine at muscarinic receptors
-
Lazareno, S.; Birdsall, N. J. M. Detection, quantitation, and verification of allosteric interactions of agents with labeled and unlabeled ligands at G protein-coupled receptors: interactions of strychnine and acetylcholine at muscarinic receptors Mol. Pharmacol. 1995, 48, 362-378
-
(1995)
Mol. Pharmacol.
, vol.48
, pp. 362-378
-
-
Lazareno, S.1
Birdsall, N.J.M.2
-
41
-
-
1842333847
-
Positive cooperativity of acetylcholine and other agonists with allosteric ligands on muscarinic acetylcholine receptors
-
Jakubik, J.; Bacakova, L.; El-Fakahany, E. E.; Tucek, S. Positive cooperativity of acetylcholine and other agonists with allosteric ligands on muscarinic acetylcholine receptors Mol. Pharmacol. 1997, 52, 172-179
-
(1997)
Mol. Pharmacol.
, vol.52
, pp. 172-179
-
-
Jakubik, J.1
Bacakova, L.2
El-Fakahany, E.E.3
Tucek, S.4
-
42
-
-
0028815463
-
Probing of the location of the allosteric site on m1 muscarinic receptors by site-directed mutagenesis
-
Matsui, H. S.; Lazareno, S.; Birdsall, N. J. M. Probing of the location of the allosteric site on m1 muscarinic receptors by site-directed mutagenesis Mol. Pharmacol. 1995, 47, 88-98
-
(1995)
Mol. Pharmacol.
, vol.47
, pp. 88-98
-
-
Matsui, H.S.1
Lazareno, S.2
Birdsall, N.J.M.3
-
43
-
-
0033945117
-
3H]scopolamine and acetylcholine at muscarinic receptor subtypes: Identification of a second allosteric site
-
3H] scopolamine and acetylcholine at muscarinic receptor subtypes: identification of a second allosteric site Mol. Pharmacol. 2000, 58, 194-207
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 194-207
-
-
Lazareno, S.1
Popham, A.2
Birdsall, N.J.M.3
-
44
-
-
0033007440
-
Allosteric interactions of quaternary strychnine and brucine derivatives with muscarinic acetylcholine receptors
-
Gharagozloo, P.; Lazareno, S.; Popham, A.; Birdsall, N. J. M. Allosteric interactions of quaternary strychnine and brucine derivatives with muscarinic acetylcholine receptors J. Med. Chem. 1999, 42, 438-445
-
(1999)
J. Med. Chem.
, vol.42
, pp. 438-445
-
-
Gharagozloo, P.1
Lazareno, S.2
Popham, A.3
Birdsall, N.J.M.4
-
46
-
-
0030218059
-
Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation
-
Kostenis, E.; Mohr, K. Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation Trends Pharmacol. Sci. 1996, 17, 280-283
-
(1996)
Trends Pharmacol. Sci.
, vol.17
, pp. 280-283
-
-
Kostenis, E.1
Mohr, K.2
-
47
-
-
0025121206
-
Muscarinic acetylcholine receptors. Peptide sequencing identifies residues involved in antagonist binding and disulfide bond formation
-
Kurtenbach, E.; Curtis, C. A. M.; Pedder, E. K.; Aitken, A.; Harris, A. C. M.; Hulme, E. C. Muscarinic acetylcholine receptors. Peptide sequencing identifies residues involved in antagonist binding and disulfide bond formation J. Biol. Chem. 1990, 265, 13702-13708
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 13702-13708
-
-
Kurtenbach, E.1
Curtis, C.A.M.2
Pedder, E.K.3
Aitken, A.4
Harris, A.C.M.5
Hulme, E.C.6
-
48
-
-
79960176452
-
Progress in structure based drug design for G protein-coupled receptors
-
Congreve, M.; Langmead, C. J.; Mason, J. S.; Marshall, F. H. Progress in structure based drug design for G protein-coupled receptors J. Med. Chem. 2011, 54, 4283-4311
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4283-4311
-
-
Congreve, M.1
Langmead, C.J.2
Mason, J.S.3
Marshall, F.H.4
-
49
-
-
84981779372
-
Zwischenmolekulare energiewanderung und fluoreszenz
-
Förster, T. Zwischenmolekulare energiewanderung und fluoreszenz Ann. Phys. (Leipzig) 1948, 2, 55-75
-
(1948)
Ann. Phys. (Leipzig)
, vol.2
, pp. 55-75
-
-
Förster, T.1
-
50
-
-
0036892882
-
Analogs of WIN 62,577 define a second allosteric site on muscarinic receptors
-
Lazareno, S.; Popham, A.; Birdsall, N. J. M. Analogs of WIN 62,577 define a second allosteric site on muscarinic receptors Mol. Pharmacol. 2002, 62, 1492-1505
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 1492-1505
-
-
Lazareno, S.1
Popham, A.2
Birdsall, N.J.M.3
-
51
-
-
0037329292
-
Structure and activation of muscarinic acetylcholine receptors
-
Hulme, E. C.; Lu, Z. L.; Saldanha, J. W.; Bee, M. S. Structure and activation of muscarinic acetylcholine receptors Biochem. Soc. Trans. 2003, 31, 29-34
-
(2003)
Biochem. Soc. Trans.
, vol.31
, pp. 29-34
-
-
Hulme, E.C.1
Lu, Z.L.2
Saldanha, J.W.3
Bee, M.S.4
-
52
-
-
33748643600
-
The predicted 3D structure of the human M1 muscarinic acetylcholine receptor with agonist and antagonist bound
-
Peng, J. Y.; Vaidehi, N.; Hall, S. E.; Goddard, W. A The predicted 3D structure of the human M1 muscarinic acetylcholine receptor with agonist and antagonist bound ChemMedChem 2006, 1, 878-890
-
(2006)
ChemMedChem
, vol.1
, pp. 878-890
-
-
Peng, J.Y.1
Vaidehi, N.2
Hall, S.E.3
Goddard, W.A.4
-
53
-
-
0034705362
-
Evidence for a tandem two-site model of ligand binding to muscarinic acetylcholine receptors
-
Jakubik, J.; El-Fakahany, E. E.; Tucek, S. Evidence for a tandem two-site model of ligand binding to muscarinic acetylcholine receptors J. Biol. Chem. 2000, 275, 18836-18844
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 18836-18844
-
-
Jakubik, J.1
El-Fakahany, E.E.2
Tucek, S.3
-
54
-
-
45749136445
-
Allosteric modulation of muscarinic acetylcholine receptors
-
Gregory, K. J.; Sexton, P. M.; Christopoulos, A. Allosteric modulation of muscarinic acetylcholine receptors Curr. Neuropharmacol. 2007, 5, 157-167
-
(2007)
Curr. Neuropharmacol.
, vol.5
, pp. 157-167
-
-
Gregory, K.J.1
Sexton, P.M.2
Christopoulos, A.3
-
55
-
-
0038575799
-
3H]dimethyl-W84 at the common allosteric site of muscarinic M2 receptors
-
3H]dimethyl-W84 at the common allosteric site of muscarinic M2 receptors Mol. Pharmacol. 2003, 64, 180-190
-
(2003)
Mol. Pharmacol.
, vol.64
, pp. 180-190
-
-
Tränkle, C.1
Weyand, O.2
Voigländer, U.3
Mynett, A.4
Lazareno, S.5
Birdsall, N.J.M.6
Mohr, K.7
-
56
-
-
0035860802
-
The neurokinin A receptor activates calcium and cAMP responses through distinct conformational states
-
Palanché, T.; Ilien, B.; Zoffmann, S.; Reck, M.-P.; Bucher, B.; Edelstein, S.; Galzi, J.-L. The neurokinin A receptor activates calcium and cAMP responses through distinct conformational states J. Biol. Chem. 2001, 276, 34853-34861
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 34853-34861
-
-
Palanché, T.1
Ilien, B.2
Zoffmann, S.3
Reck, M.-P.4
Bucher, B.5
Edelstein, S.6
Galzi, J.-L.7
-
58
-
-
57649170953
-
A novel mechanism of G protein-coupled receptor functional selectivity. Muscarinic partial agonist McN-A-343 as a bitopic orthosteric/allosteric ligand
-
Valant, C.; Gregory, K. J.; Hall, N. E.; Scammels, P. J.; Lew, M. J.; Sexton, P. M.; Christopoulos, A. A novel mechanism of G protein-coupled receptor functional selectivity. Muscarinic partial agonist McN-A-343 as a bitopic orthosteric/allosteric ligand J. Biol. Chem. 2008, 283, 29312-29321
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 29312-29321
-
-
Valant, C.1
Gregory, K.J.2
Hall, N.E.3
Scammels, P.J.4
Lew, M.J.5
Sexton, P.M.6
Christopoulos, A.7
-
59
-
-
77951136172
-
Hybrid ortho/allosteric ligands for the adenosine A1 receptor
-
Narlawar, R.; Lane, J. R.; Doddareddy, M.; Lin, J.; Brussee, J.; Ijzerman, A. P. Hybrid ortho/allosteric ligands for the adenosine A1 receptor J. Med. Chem. 2010, 53, 3028-3037
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3028-3037
-
-
Narlawar, R.1
Lane, J.R.2
Doddareddy, M.3
Lin, J.4
Brussee, J.5
Ijzerman, A.P.6
-
60
-
-
59649112659
-
Dualsteric GPCR targeting: A novel route to binding and signaling pathway selectivity
-
Antony, J.; Kellershohn, K.; Mohr-Andrä, M.; Kebig, A.; Prilla, S.; Muth, M.; Heller, E.; Disingrini, T.; Dallanoce, C.; Bertoni, S.; Schrobang, J.; Tränkle, C.; Kostenis, E.; Christopoulos, A.; Höltje, H. D.; Barocelli, E.; De Amici, M.; Holzgrabe, U.; Mohr, K. Dualsteric GPCR targeting: a novel route to binding and signaling pathway selectivity FASEB J. 2009, 23, 442-450
-
(2009)
FASEB J.
, vol.23
, pp. 442-450
-
-
Antony, J.1
Kellershohn, K.2
Mohr-Andrä, M.3
Kebig, A.4
Prilla, S.5
Muth, M.6
Heller, E.7
Disingrini, T.8
Dallanoce, C.9
Bertoni, S.10
Schrobang, J.11
Tränkle, C.12
Kostenis, E.13
Christopoulos, A.14
Höltje, H.D.15
Barocelli, E.16
De Amici, M.17
Holzgrabe, U.18
Mohr, K.19
-
61
-
-
67650489125
-
Orthosteric/allosteric bitopic hybrids. Going hybrid at GPCRs
-
Valant, C.; Sexton, P. M.; Christopoulos, A. Orthosteric/allosteric bitopic hybrids. Going hybrid at GPCRs Mol. Interventions 2009, 9, 125-135
-
(2009)
Mol. Interventions
, vol.9
, pp. 125-135
-
-
Valant, C.1
Sexton, P.M.2
Christopoulos, A.3
-
62
-
-
84858024834
-
-
Molecular Probes.
-
Molecular Probes. http://www.probes.com/handbook/.
-
-
-
|