-
1
-
-
0025232511
-
Serotonin Receptors: Clinical Implications
-
Glennon, R. A. Serotonin Receptors: Clinical Implications. Neurosci. Behav. Rev. 1990, 14, 35—47.
-
(1990)
Neurosci. Behav. Rev.
, vol.14
, pp. 35-47
-
-
Glennon, R.A.1
-
2
-
-
0012073075
-
Molecular/Cell Biology of G-Protein Coupled CNS Receptors
-
Gluchowski, C.; Branchek, T. A.; Weinshank, R. L.; Hartig, P. R. Molecular/Cell Biology of G-Protein Coupled CNS Receptors. Annu. Rep. Med. Chem. 1993, 28, 29-38.
-
(1993)
Annu. Rep. Med. Chem.
, vol.28
, pp. 29-38
-
-
Gluchowski, C.1
Branchek, T.A.2
Weinshank, R.L.3
Hartig, P.R.4
-
3
-
-
0026633428
-
Molecular Biology of the 5-HTi Receptor Subfamily
-
Hartig, P. R.; Adham, N.; Zgombick, J.; Weinshank, R.; Branchek, T. Molecular Biology of the 5-HTi Receptor Subfamily. Drug Dev. Res. 1992, 26, 215-224.
-
(1992)
Drug Dev. Res.
, vol.26
, pp. 215-224
-
-
Hartig, P.R.1
Adham, N.2
Zgombick, J.3
Weinshank, R.4
Branchek, T.5
-
4
-
-
0023188864
-
Buspirone Hydrochloride (Bespar®; Buspai®)-A New Anxiolytic Agent
-
Robinson, C. P. Buspirone Hydrochloride (Bespar®; Buspai®)-A New Anxiolytic Agent. Drugs Today 1987, 23, 311-319.
-
(1987)
Drugs Today
, vol.23
, pp. 311-319
-
-
Robinson, C.P.1
-
5
-
-
0026357349
-
Serotonin Receptor Subtypes and Neuropsychiatic Diseases: Focus on 5-HTm and 5-HTg Receptor Agents
-
Peroutka, S. J. VI. Serotonin Receptor Subtypes and Neuropsychiatic Diseases: Focus on 5-HTm and 5-HTg Receptor Agents. Pharmacol. Rev. 1991, 43, 579-586.
-
(1991)
Pharmacol. Rev.
, vol.43
, pp. 579-586
-
-
Peroutka, S.J.1
-
6
-
-
0027336957
-
(±) 3-Amino-6-carboxamido-1,2,3,4-tetrahydrocarbazole: A Conformationally Restricted Analogue of 5-Carboxamidotryptamine with Selectivity for the Serotonin 5-HTm Receptor
-
King, F. D.; Brown, A. M.; Gaster, L. M.; Kaumann, A. J.; Medhurst, A. D.; Parker, S. G.; Parsons, A. A.; Patch, T. L.; Raval, P. (±) 3-Amino-6-carboxamido-1,2,3,4-tetrahydrocarbazole: A Conformationally Restricted Analogue of 5-Carboxamidotryptamine with Selectivity for the Serotonin 5-HTm Receptor. J. Med. Chem. 1993, 36, 1918-1919.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1918-1919
-
-
King, F.D.1
Brown, A.M.2
Gaster, L.M.3
Kaumann, A.J.4
Medhurst, A.D.5
Parker, S.G.6
Parsons, A.A.7
Patch, T.L.8
Raval, P.9
-
7
-
-
0027246318
-
Synthesis and Serotonergic Activity of 5-(Oxadiazolyl)tryptamines: Potent Agonists for 5-HTm Receptors
-
Street, L. J.; Baker, R.; Castro, J. L.; Chambers, M. S.; Guiblin, A. R.; Hobbs, S. C.; Matassa, V. C.; Reeve, A. J.; Beer, M. S.; Middlemiss, D. N.; Noble, A. J.; Stanton, J. A.; Scholey, K.; Hargreaves, J. Synthesis and Serotonergic Activity of 5-(Oxadiazolyl)tryptamines: Potent Agonists for 5-HTm Receptors. J. Med. Chem. 1993, 36, 1529-1538.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1529-1538
-
-
Street, L.J.1
Baker, R.2
Castro, J.L.3
Chambers, M.S.4
Guiblin, A.R.5
Hobbs, S.C.6
Matassa, V.C.7
Reeve, A.J.8
Beer, M.S.9
Middlemiss, D.N.10
Noble, A.J.11
Stanton, J.A.12
Scholey, K.13
Hargreaves, J.14
-
8
-
-
0025280635
-
K 3-(1,2,5,6-Tetrahydropyrid-4-yl)-pyrrolo[3,2-b]pyrid-5-one: A Potent mid Selective Serotonin (5-HTm) Ligand and Rotationally Restricted Phenolic Analog of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indole
-
Macor, J. E.; Burkhart, C. A.; Heym, J. H.; Ives, J. L.; Lebel, L. A.; Newman, M. E.; Nielsen, J. A.; Ryan, K.; Schulz, D. W.; Tbrgersen, L. K.; Koe, B. K 3-(1,2,5,6-Tetrahydropyrid-4-yl)-pyrrolo[3,2-b]pyrid-5-one: A Potent mid Selective Serotonin (5-HTm) Ligand and Rotationally Restricted Phenolic Analog of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indole. J. Med. Chem. 1990, 33, 2087-2093.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2087-2093
-
-
Macor, J.E.1
Burkhart, C.A.2
Heym, J.H.3
Ives, J.L.4
Lebel, L.A.5
Newman, M.E.6
Nielsen, J.A.7
Ryan, K.8
Schulz, D.W.9
Tbrgersen, L.K.10
Koe, B.11
-
9
-
-
0004447314
-
Synthesis of a Rotationally Restricted Phenolic Analog of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl) indole (RU-24969)
-
Macor, J. E.; Newman, M. E. Synthesis of a Rotationally Restricted Phenolic Analog of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl) indole (RU-24969). Heterocycles 1990, 31, 805-809.
-
(1990)
Heterocycles
, vol.31
, pp. 805-809
-
-
Macor, J.E.1
Newman, M.E.2
-
10
-
-
0011932637
-
Synthesis of Some Conformationally Restricted Serotonin Analogs
-
Macor, J. E.; Ryan, K. Synthesis of Some Conformationally Restricted Serotonin Analogs. Heterocycles 1990, 31, 1497-1504.
-
(1990)
Heterocycles
, vol.31
, pp. 1497-1504
-
-
Macor, J.E.1
Ryan, K.2
-
11
-
-
0025727992
-
Synthesis of a Dihydropyrano[3,2-elindóle as a Rotationally Restricted Phenolic Analog of the Neurotransmitter Serotonin
-
Macor, J. E.; Newman, M. E. Synthesis of a Dihydropyrano[3,2-elindóle as a Rotationally Restricted Phenolic Analog of the Neurotransmitter Serotonin. Tetrahedron Lett. 1991, 32, 3345-3348.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 3345-3348
-
-
Macor, J.E.1
Newman, M.E.2
-
12
-
-
0026504586
-
The Synthesis of Pyrano[3,2-e]indoles and Pyrano[2,3-f]indoles as Rotationally Restricted Analogs of the Neurotransmitter Serotonin
-
Macor, J. E.; Ryan, K.; Newman, M. E. The Synthesis of Pyrano[3,2-e]indoles and Pyrano[2,3-f]indoles as Rotationally Restricted Analogs of the Neurotransmitter Serotonin. Tetrahedron 1992, 48, 1039-1052.
-
(1992)
Tetrahedron
, vol.48
, pp. 1039-1052
-
-
Macor, J.E.1
Ryan, K.2
Newman, M.E.3
-
13
-
-
0026754567
-
1-(2-Aminoethyl)-6-methyl-8,9-dihydropyrano[3,2-elindole: A Rotationally Restricted Phenolic Analog of the Neurotransmitter Serotonin and Agonist Selective for Serotonin (5-HT2) Receptors
-
Macor, J. E.; Fox, C. B.; Johnson, C.; Koe, B. K.; Lebel, L. A.; Zorn, S. H. 1-(2-Aminoethyl)-6-methyl-8,9-dihydropyrano[3,2-elindole: A Rotationally Restricted Phenolic Analog of the Neurotransmitter Serotonin and Agonist Selective for Serotonin (5-HT2) Receptors. J. Med. Chem. 1992, 35, 3625-3632.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3625-3632
-
-
Macor, J.E.1
Fox, C.B.2
Johnson, C.3
Koe, B.K.4
Lebel, L.A.5
Zorn, S.H.6
-
14
-
-
0026462892
-
The Synthesis and Serotonergic Pharmacology of the Enantiomers of 3-[(N-Methylpynolidin-2-yl)methyl]-5-methoxy-1H-indole: Discovery of Stereogenic Differentiation in the Aminoethyl Sidechain of the Neurotransmitter Serotonin
-
Macor, J. E.; Blake, J.; Fox, C. A.; Johnson, C.; Koe, B. K.; Lebel, L. A.; Morrone, J. M.; Ryan, K.; Schmidt, A. W.; Schulz, D. W.; Zorn, S. H. The Synthesis and Serotonergic Pharmacology of the Enantiomers of 3-[(N-Methylpynolidin-2-yl)methyl]-5-methoxy-1H-indole: Discovery of Stereogenic Differentiation in the Aminoethyl Sidechain of the Neurotransmitter Serotonin. J. Med. Chem. 1992, 35, 4503-4505.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4503-4505
-
-
Macor, J.E.1
Blake, J.2
Fox, C.A.3
Johnson, C.4
Koe, B.K.5
Lebel, L.A.6
Morrone, J.M.7
Ryan, K.8
Schmidt, A.W.9
Schulz, D.W.10
Zorn, S.H.11
-
15
-
-
0027056036
-
Synthesis of a Conformationally Restricted Analog of the Anti-migraine Drug, Sumatriptan
-
Macor, J. E.; Blank, D. H.; Post, R. J.; Ryan, K. Synthesis of a Conformationally Restricted Analog of the Anti-migraine Drug, Sumatriptan. Tetrahedron Lett. 1992, 33, 8011-8014.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 8011-8014
-
-
Macor, J.E.1
Blank, D.H.2
Post, R.J.3
Ryan, K.4
-
16
-
-
0027982809
-
The Synthesis of Conformationally/Rotationally Restricted Analogs of the Neurotransmitter Serotonin
-
Macor, J. E.; Blank, D. H.; Post, R. J. The Synthesis of Conformationally/Rotationally Restricted Analogs of the Neurotransmitter Serotonin. Tetrahedron Lett. 1994, 35, 45—48.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 45-48
-
-
Macor, J.E.1
Blank, D.H.2
Post, R.J.3
-
17
-
-
0027524103
-
Simple Synthesis of 5-Amino-3-(2-dimethylaminoethyl)indole [5-amino-N,N-dimethyltryptamine]
-
Macor, J. E.; Ryan, K. A. Simple Synthesis of 5-Amino-3-(2-dimethylaminoethyl)indole [5-amino-N,N-dimethyltryptamine]. Synth. Commun. 1993, 23, 65-72.
-
(1993)
Synth. Commun.
, vol.23
, pp. 65-72
-
-
Macor, J.E.1
Ryan, K.A.2
-
18
-
-
0027515704
-
Conformationally restricted sumatriptan analogues, CP-122,288 and CP-122,638 exhibit enhanced potency against neurogenic inflammation in dura matter
-
Lee, W. S.; Moskowitz, M. A. Conformationally restricted sumatriptan analogues, CP-122,288 and CP-122,638 exhibit enhanced potency against neurogenic inflammation in dura matter. Brain Res. 1993, 626, 303-305.
-
(1993)
Brain Res.
, vol.626
, pp. 303-305
-
-
Lee, W.S.1
Moskowitz, M.A.2
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