-
1
-
-
0028183017
-
International Union of Pharmacology Classification of Receptors for 5-Hydroxytryptamine (Serotonin)
-
Hoyer, D.; Clarke, D. E.; Fozard, J. R.; Hartig, P. R.; Martin, G. R.; Mylecharane, E. J.; Saxena, P. R.; Humphrey, P. P. A. International Union of Pharmacology Classification of Receptors for 5-Hydroxytryptamine (Serotonin). Pharmacol. Rev. 1994, 46 (2), 157.
-
(1994)
Pharmacol. Rev.
, vol.46
, Issue.2
, pp. 157
-
-
Hoyer, D.1
Clarke, D.E.2
Fozard, J.R.3
Hartig, P.R.4
Martin, G.R.5
Mylecharane, E.J.6
Saxena, P.R.7
Humphrey, P.P.A.8
-
4
-
-
0029867011
-
4 receptors: Physiology, pharmacology and therapeutic potential
-
4 receptors: physiology, pharmacology and therapeutic potential. Exp. Opin. Invest. Drugs 1996, 5 (4), 373.
-
(1996)
Exp. Opin. Invest. Drugs
, vol.5
, Issue.4
, pp. 373
-
-
Eglen, R.M.1
Hegde, S.S.2
-
5
-
-
0024263139
-
Nonclassical 5-hydroxytryptamine receptor positively coupled with adenylate cyclase in the central nervous system
-
Dumuis, A.; Bouhelal, R.; Sebben, M.; Cory, R.; Bockaert, J. A. nonclassical 5-hydroxytryptamine receptor positively coupled with adenylate cyclase in the central nervous system. Mol. Pharmacol. 1988, 34, 880.
-
(1988)
Mol. Pharmacol.
, vol.34
, pp. 880
-
-
Dumuis, A.1
Bouhelal, R.2
Sebben, M.3
Cory, R.4
Bockaert, J.A.5
-
6
-
-
0028978023
-
The 5-HT4 receptor: Molecular cloning and pharmacological characterization of two splice variants
-
(a) Gerald, C.; Adham, N.; Kao, H.-T.; Olsen, M. A.; Laz, T. M.; Schechter, L. E.; Bard, J. A.; Vaysse, P. J. J.; Hartig, P. R.; Branchek, T. A.; Weinshank, R. L. The 5-HT4 receptor: molecular cloning and pharmacological characterization of two splice variants. EMBO J. 1995, 14, 2806.
-
(1995)
EMBO J.
, vol.14
, pp. 2806
-
-
Gerald, C.1
Adham, N.2
Kao, H.-T.3
Olsen, M.A.4
Laz, T.M.5
Schechter, L.E.6
Bard, J.A.7
Vaysse, P.J.J.8
Hartig, P.R.9
Branchek, T.A.10
Weinshank, R.L.11
-
7
-
-
0029156503
-
Expression of Serotonin receptor mRNAs in blood vessels
-
(b) Ullmer, C.; Schmuck, K.; Kalkman, H. O.; Lubbert, H. Expression of Serotonin receptor mRNAs in blood vessels. FEBS Lett. 1995, 370, 215.
-
(1995)
FEBS Lett.
, vol.370
, pp. 215
-
-
Ullmer, C.1
Schmuck, K.2
Kalkman, H.O.3
Lubbert, H.4
-
8
-
-
0026611585
-
4 receptor subtype inhibits potassium current in colliculi neurons via activation of a cyclic AMP-dependent protein kinase
-
4 receptor subtype inhibits potassium current in colliculi neurons via activation of a cyclic AMP-dependent protein kinase. Br. J. Pharmacol. 1992, 105, 973.
-
(1992)
Br. J. Pharmacol.
, vol.105
, pp. 973
-
-
Fagni, L.1
Dumuis, A.2
Sebben, M.3
Bockaert, J.4
-
9
-
-
0030431051
-
4 Receptor Antagonist: Comparison to Cisapride and RS23597-190
-
4 Receptor Antagonist: Comparison to Cisapride and RS23597-190. J. Pharmacol. Exp. Ther. 1996, 277, 97.
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.277
, pp. 97
-
-
Cohen, M.1
Bloomquist, W.2
Schaus, J.3
Thompson, D.4
Susemichel, A.5
Calligaro, D.6
Cohen, I.7
-
11
-
-
0028173139
-
4 Receptors in Rat but not Guinea Pig, Rabbit or Dog Esophageal Smooth Muscle
-
4 Receptors in Rat but not Guinea Pig, Rabbit or Dog Esophageal Smooth Muscle. Gen. Pharmacol. 1994, 25 (6), 1143.
-
(1994)
Gen. Pharmacol.
, vol.25
, Issue.6
, pp. 1143
-
-
Cohen, M.L.1
Susemichel, A.D.2
Bloomquist, W.3
Robertson, D.W.4
-
12
-
-
0028270273
-
GR 113, 808: A novel selective antagonist with high affinity at the 5-HT4 receptor
-
Gale, J. D.; Grossman, C. J.; Whitehead, J. W. F.; Oxford, A. W.; Bunce, K. T.; Humphrey, P. P. A. GR 113, 808: a novel selective antagonist with high affinity at the 5-HT4 receptor. Br. J. Pharmacol. 1994, 111, 332.
-
(1994)
Br. J. Pharmacol.
, vol.111
, pp. 332
-
-
Gale, J.D.1
Grossman, C.J.2
Whitehead, J.W.F.3
Oxford, A.W.4
Bunce, K.T.5
Humphrey, P.P.A.6
-
13
-
-
0028343154
-
4 receptor antagonist, on guinea pig distal colon
-
4 receptor antagonist, on guinea pig distal colon. Br. J. Pharmacol. 1994, 112, 789.
-
(1994)
Br. J. Pharmacol.
, vol.112
, pp. 789
-
-
Wardel, K.A.1
Ellis, E.S.2
Baxter, G.S.3
Kennett, G.A.4
Gaster, L.M.5
Sanger, G.J.6
-
14
-
-
0028004493
-
4 Receptor Antagonist RS-23597 are High Affinity Partial Agonists
-
4 Receptor Antagonist RS-23597 are High Affinity Partial Agonists. Bioorg. Med. Chem. Lett. 1994, 20, 2477.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 2477
-
-
Clark, R.D.1
Jahangir, A.2
Langsten, J.A.3
Weinhardt, K.K.4
Miller, A.B.5
Leung, E.6
Eglen, R.M.7
-
15
-
-
0030014935
-
4 receptor antagonism by SB 207266
-
4 receptor antagonism by SB 207266. Br. J. Pharmacol. 1996, 118, 665.
-
(1996)
Br. J. Pharmacol.
, vol.118
, pp. 665
-
-
Wardle, K.A.1
Bingham, S.2
Ellis, E.S.3
Gaster, L.M.4
Rushant, B.5
Smith, M.I.6
Sanger, G.J.7
-
16
-
-
0029144097
-
4 receptor antagonist
-
4 receptor antagonist. BioOrg. Med. Chem. Lett. 1995, 5, 2119.
-
(1995)
BioOrg. Med. Chem. Lett.
, vol.5
, pp. 2119
-
-
Clark, R.D.1
Jahangir, A.2
Flippen, L.A.3
Miller, A.B.4
Leung, E.5
Bonhaus, D.W.6
Wong, E.H.F.7
Johnson, L.G.8
Eglen, R.M.9
-
17
-
-
0029897159
-
Hydride Reagents for Stereoselective Reductive Amination. An Improved Preparation of 3-endo-Tropanamine
-
McGill, J.; LaBell, E.; Williams, M. Hydride Reagents for Stereoselective Reductive Amination. An Improved Preparation of 3-endo-Tropanamine. Tetrahedron Lett. 1996, 37, 3977.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 3977
-
-
McGill, J.1
Labell, E.2
Williams, M.3
-
18
-
-
0343278751
-
Indazole Analogue of Tryptamine: A New Synthesis of Indazoles
-
Ainsworth, C. Indazole Analogue of Tryptamine: A New Synthesis of Indazoles. J. Am. Chem. Soc. 1957, 79, 5242.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 5242
-
-
Ainsworth, C.1
-
19
-
-
15144343246
-
-
note
-
While the alkylation of indazole-3-carboxylic esters and of indazole itself is known to give regiochemical mixtures of N-1 and N-2 alkylated products, the alkylation of amide 12a predominantly gave the N-l alkylated product. It is believed that internal hydrogen bonding between the amide N-H and N-2 (i) deactivates N-2 to alkylation and directs alkylation to N-1.
-
-
-
-
20
-
-
0025369707
-
3 Receptor Antagonists
-
3 Receptor Antagonists. J. Med. Chem. 1990, 33, 2101.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2101
-
-
Turconi, M.1
Nicola, M.2
Quintero, M.G.3
Maiocchi, L.4
Micheletti, R.5
Giraldo, E.6
Donetti, A.7
-
22
-
-
0026527430
-
3 receptor antagonist: Synthesis and structure-activity relationships
-
3 receptor antagonist: synthesis and structure-activity relationships. J. Med. Chem. 1992, 35, 310.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 310
-
-
Robertson, D.1
Lacefield, W.2
Bloomquist, W.3
Pfeifer, W.4
Simon, R.5
Cohen, M.6
-
23
-
-
0025761899
-
Investigation into the 5-hydroxytryptamine receptor mediating smooth muscle relaxation in the rat oesophagus
-
(a) Reeves, J. J.; Bunce, K. T.; Humphrey, P. P. A. Investigation into the 5-hydroxytryptamine receptor mediating smooth muscle relaxation in the rat oesophagus. Br. J. Pharmacol. 1991, 103, 1067.
-
(1991)
Br. J. Pharmacol.
, vol.103
, pp. 1067
-
-
Reeves, J.J.1
Bunce, K.T.2
Humphrey, P.P.A.3
-
25
-
-
15144346833
-
-
See ref 11 for another example in which amides possessed higher efficacy (i.e., greater agonist activity) than the corresponding esters
-
See ref 11 for another example in which amides possessed higher efficacy (i.e., greater agonist activity) than the corresponding esters.
-
-
-
-
26
-
-
0026335156
-
4 receptors and potential therapeutic implications
-
4 receptors and potential therapeutic implications. Drugs Future 1991, 16, 1011.
-
(1991)
Drugs Future
, vol.16
, pp. 1011
-
-
Turconi, M.1
Schiantarelli, P.2
Borsini, F.3
Rizzi, C.4
Ladinsky, H.5
Donetti, A.6
-
29
-
-
0013227460
-
Substituted Benzamides. The development of selective dopamine antagonists
-
Dahlbom, R., Nilsson, J. L. G., Eds.: Swedish Pharmaceutical Press: Stockholm
-
de Paulis, T. Substituted Benzamides. The development of selective dopamine antagonists. In VIIth International Symposium on Medicinal Chemistry, Proceedings, Vol. 1; Dahlbom, R., Nilsson, J. L. G., Eds.: Swedish Pharmaceutical Press: Stockholm, 1985; p 405.
-
(1985)
VIIth International Symposium on Medicinal Chemistry, Proceedings
, vol.1
, pp. 405
-
-
De Paulis, T.1
-
30
-
-
15144341486
-
-
b = 8.40) (Cohen, M. L.; Robertson, D. W.; Susemichel, A. D.; Krushinski, J. K. Unpublished results)
-
b = 8.40) (Cohen, M. L.; Robertson, D. W.; Susemichel, A. D.; Krushinski, J. K. Unpublished results).
-
-
-
-
31
-
-
0021812342
-
Identification of serotonin M-receptor subtypes and their specific blockade by a new class of drugs
-
Richardson, B. P.; Engel, G.; Donatsch, P.; Stadler, P. A. Identification of serotonin M-receptor subtypes and their specific blockade by a new class of drugs. Nature 1985, 316, 126.
-
(1985)
Nature
, vol.316
, pp. 126
-
-
Richardson, B.P.1
Engel, G.2
Donatsch, P.3
Stadler, P.A.4
-
32
-
-
0024477141
-
3 Receptor antagonist Properties of ICS 205-930, GR38032F and Zacopride
-
3 Receptor antagonist Properties of ICS 205-930, GR38032F and Zacopride. J. Pharmacol. Exp. Ther. 1989, 248, 197.
-
(1989)
J. Pharmacol. Exp. Ther.
, vol.248
, pp. 197
-
-
Cohen, M.C.1
Bloomquist, W.2
Gidda, J.S.3
Lacefield, W.4
-
34
-
-
0010382945
-
3 Antagonist Binding Site
-
Hamon, M.; Ed.; Academic Press: London, Chapter 4
-
3 Receptors; Hamon, M.; Ed.; Academic Press: London, 1995; Chapter 4, p 59.
-
(1995)
3 Receptors
, pp. 59
-
-
Gozlan, H.1
Langlois, M.2
-
35
-
-
0018332473
-
3H]-prazosin to rat brain alpha-adrenergic receptors
-
3H]-prazosin to rat brain alpha-adrenergic receptors. Eur. J. Pharmacol. 1979, 55, 323.
-
(1979)
Eur. J. Pharmacol.
, vol.55
, pp. 323
-
-
Greengrass, P.1
Bremner, R.2
-
37
-
-
0028986803
-
4 receptor function
-
4 receptor function. J. Pharm. Pharmacol. 1995, 47, 219.
-
(1995)
J. Pharm. Pharmacol.
, vol.47
, pp. 219
-
-
Bingham, S.1
King, B.F.2
Rushant, B.3
Smith, M.I.4
Gaster, L.M.5
Sanger, G.J.6
-
39
-
-
0027239618
-
4 receptor antagonist
-
4 receptor antagonist. Br. J. Pharmacol. 1993, 110, 119.
-
(1993)
Br. J. Pharmacol.
, vol.110
, pp. 119
-
-
Eglen, R.M.1
Bley, K.2
Bonhous, D.W.3
Clark, R.D.4
Hegde, S.S.5
Johnson, L.G.6
Leung, E.7
Wong, E.H.F.8
-
40
-
-
15144355161
-
-
note
-
4 receptor antagonist activity in vitro, yet no ex vivo inhibition of esophageal relaxation to serotonin occurred at a dose (1.0 mg/kg) 10-fold higher than the inhibitory dose of 8. This finding is consistent with the conclusion that the activity of compounds in this ex vivo assay following oral administration is due to systemic absorption rather than through localized effects.
-
-
-
-
41
-
-
15144346314
-
-
See ref 6 for a detailed report on the pharmacology of 8
-
See ref 6 for a detailed report on the pharmacology of 8.
-
-
-
|