-
1
-
-
0003174188
-
Practice guideline for the treatment of patients with schizophrenia. American Psychiatric Association
-
Practice guideline for the treatment of patients with schizophrenia. American Psychiatric Association. Am. J. Psychiatry 1997, 154,1-63.
-
(1997)
Am. J. Psychiatry
, vol.154
, pp. 1-63
-
-
-
2
-
-
0024247522
-
The current status of the dopamine hypothesis of schizophrenia
-
Carlsson, A. The current status of the dopamine hypothesis of schizophrenia. Neurovsychovharmacology 1988, 1, 179-186.
-
(1988)
Neurovsychovharmacology
, vol.1
, pp. 179-186
-
-
Carlsson, A.1
-
3
-
-
0024468417
-
Clinical studies on the mechanism of action of clozapine: The dopamine-serotonin hypothesis of schizophrenia
-
Meltzer, H. Y. Clinical studies on the mechanism of action of clozapine: the dopamine-serotonin hypothesis of schizophrenia. Psy-chovharmacology (Berlin) 1989, 99, S18-S27.
-
(1989)
Psy-chovharmacology (Berlin)
, vol.99
-
-
Meltzer, H.Y.1
-
4
-
-
0032895987
-
The use of atypical antipsychotics in the management of schizophrenia
-
Campbell, M.; Young, P. I.; Bateman, D. N.; Smith, J. M.; Thomas, S. H. The use of atypical antipsychotics in the management of schizophrenia. Br. J. Clin. Pharmacol. 1999, 47, 13-22.
-
(1999)
Br. J. Clin. Pharmacol
, vol.47
, pp. 13-22
-
-
Campbell, M.1
Young, P.I.2
Bateman, D.N.3
Smith, J.M.4
Thomas, S.H.5
-
5
-
-
0035990397
-
Olanzapine-associated diabetes mellitus
-
Koller, E. A.; Doraiswamy, P. M. Olanzapine-associated diabetes mellitus. Pharmacotherapy 2002, 22, 841-852.
-
(2002)
Pharmacotherapy
, vol.22
, pp. 841-852
-
-
Koller, E.A.1
Doraiswamy, P.M.2
-
6
-
-
0034598111
-
Atypical antipsychotics in the treatment of schizophrenia: Systematic overview and meta-regression analysis
-
Geddes, J.; Freemantle, N.; Harrison, P.; Bebbington, P. Atypical antipsychotics in the treatment of schizophrenia: systematic overview and meta-regression analysis. Br. Med. J. 2000, 321, 1371-1376.
-
(2000)
Br. Med. J
, vol.321
, pp. 1371-1376
-
-
Geddes, J.1
Freemantle, N.2
Harrison, P.3
Bebbington, P.4
-
7
-
-
0036035565
-
-
McGawin, J. K.; Goa, K. L. Aripiprazole. CNS Drugs 2002, 16, 779-786.
-
McGawin, J. K.; Goa, K. L. Aripiprazole. CNS Drugs 2002, 16, 779-786.
-
-
-
-
8
-
-
0037321460
-
Aripiprazole: Efficacy and Tolerability Profile of a Novel-Acting Atypical Antipsychotic
-
Buckley, P. F. Aripiprazole: Efficacy and Tolerability Profile of a Novel-Acting Atypical Antipsychotic. Drugs Today 2003, 2, 145-151.
-
(2003)
Drugs Today
, vol.2
, pp. 145-151
-
-
Buckley, P.F.1
-
9
-
-
0037396844
-
Novel antipsychotic agents: Recent advances in the drug treatment of schizophrenia
-
Butini, S.; Campiani, G.; De Angelis, M.; Fattorusso, C.; Nacci, V.; Fiorini, I. Novel antipsychotic agents: recent advances in the drug treatment of schizophrenia. Expert Ovin. Ther. Patents 2003,13, 425-448.
-
(2003)
Expert Ovin. Ther. Patents
, vol.13
, pp. 425-448
-
-
Butini, S.1
Campiani, G.2
De Angelis, M.3
Fattorusso, C.4
Nacci, V.5
Fiorini, I.6
-
10
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
Morphy, R.; Rankovic, Z. Designed multiple ligands. An emerging drug discovery paradigm. J. Med. Chem. 2005, 48, 6523-6543.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
11
-
-
44649091246
-
Modulation of Neuronal Excitability by Serotonin-NMDA Interactions in Prefrontal Cortex
-
Zhong, P.; Yuen, E. Y.; Yan, Z. Modulation of Neuronal Excitability by Serotonin-NMDA Interactions in Prefrontal Cortex. Mool CelL Neurosci. 2008, 38, 290-299.
-
(2008)
Mool CelL Neurosci
, vol.38
, pp. 290-299
-
-
Zhong, P.1
Yuen, E.Y.2
Yan, Z.3
-
14
-
-
0034711425
-
Binding of antipsychotic drugs to human brain receptors. Focus on newer generation compounds
-
(c) Richelson, E.; Souder, T. Binding of antipsychotic drugs to human brain receptors. Focus on newer generation compounds. Life Sci. 2000, 68, 29-39.
-
(2000)
Life Sci
, vol.68
, pp. 29-39
-
-
Richelson, E.1
Souder, T.2
-
15
-
-
0032230189
-
Effect of tandospirone on tardive dyskinesia and parkinsonian symptoms
-
Yoshida, K.; Sugita, T.; Higuchi, H.; Hishikawa, Y. Effect of tandospirone on tardive dyskinesia and parkinsonian symptoms. Eur. Psychiatry 1998, 13, 421-422.
-
(1998)
Eur. Psychiatry
, vol.13
, pp. 421-422
-
-
Yoshida, K.1
Sugita, T.2
Higuchi, H.3
Hishikawa, Y.4
-
16
-
-
0031937466
-
Reversal of haloperidol-induced extrapiramidal side effects in cebus monkeys by 8-hydroxy-2-(di-N- propylamino)tetralin and its enantiomers
-
Christoffersen, C. L.; Meltzer, L. T. Reversal of haloperidol-induced extrapiramidal side effects in cebus monkeys by 8-hydroxy-2-(di-N- propylamino)tetralin and its enantiomers. Neurovsychovharmacology 1998, 18, 399-402.
-
(1998)
Neurovsychovharmacology
, vol.18
, pp. 399-402
-
-
Christoffersen, C.L.1
Meltzer, L.T.2
-
19
-
-
0037177358
-
1A receptor
-
1A receptor. Eur. J. Pharmacol. 2002, 441, 137-140.
-
(2002)
Eur. J. Pharmacol
, vol.441
, pp. 137-140
-
-
Jordan, S.1
Koprivica, V.2
Chen, R.3
Tottori, K.4
Kikuchi, T.5
Altar, C.A.6
-
21
-
-
52949139104
-
1A receptors improve cognition in schizophrenia
-
1A receptors improve cognition in schizophrenia. Behav. Brain Res. 2008,195, 98-102.
-
(2008)
Behav. Brain Res
, vol.195
, pp. 98-102
-
-
Meltzer, H.Y.1
Sumiyoshi, T.2
-
24
-
-
40849116470
-
-
2 receptor antagonist and potential antipsychotic agent: III. Actions in models of therapeutic activity and induction of side effects. J. Pharmacol. Exv. Ther. 2008, 324, 1212-1226.
-
2 receptor antagonist and potential antipsychotic agent: III. Actions in models of therapeutic activity and induction of side effects. J. Pharmacol. Exv. Ther. 2008, 324, 1212-1226.
-
-
-
-
25
-
-
14444269458
-
New Antipsychotic Agents with Serotonin and Dopamine Antagonist Properties Based on a Pyrrolo[2,1- b][1,3]benzothiazepine Structure
-
(a) Campiani, G.; Nacci, V.; Bechelli, S.; Ciani, S. M.; Garofalo, A.; Fiorini, I.; Wikstrom, H.; de Boer, P.; Liao, Y.; Tepper, P. G.; Cagnotto, A.; Mennini, T. New Antipsychotic Agents with Serotonin and Dopamine Antagonist Properties Based on a Pyrrolo[2,1- b][1,3]benzothiazepine Structure. J. Med. Chem. 1998, 41, 3763-3772.
-
(1998)
J. Med. Chem
, vol.41
, pp. 3763-3772
-
-
Campiani, G.1
Nacci, V.2
Bechelli, S.3
Ciani, S.M.4
Garofalo, A.5
Fiorini, I.6
Wikstrom, H.7
de Boer, P.8
Liao, Y.9
Tepper, P.G.10
Cagnotto, A.11
Mennini, T.12
-
26
-
-
0037122780
-
Pyrrolo[1,3]benzothiazepine atypical antipsychotic agents. Synthesis, structure-activity relationships, molecular-modelling, and biological studies
-
(b) Campiani, G.; Butini, S.; Gemma, S.; Nacci, V.; Fattorusso, C.; Catalanotti, B.; Giorgi, G.; Cagnotto, A.; Goegan, M.; Mennini, T.; Minetti, P.; Di Cesare, M. A.; Mastroianni, D.; Scafetta, N.; Galletti, B.; Stasi, M. A.; Castorina, M.; Pacifici, L.; Ghirardi, O.; Tinti, O.; Carminati, P. Pyrrolo[1,3]benzothiazepine atypical antipsychotic agents. Synthesis, structure-activity relationships, molecular-modelling, and biological studies. J. Med. Chem. 2002, 45, 344-359.
-
(2002)
J. Med. Chem
, vol.45
, pp. 344-359
-
-
Campiani, G.1
Butini, S.2
Gemma, S.3
Nacci, V.4
Fattorusso, C.5
Catalanotti, B.6
Giorgi, G.7
Cagnotto, A.8
Goegan, M.9
Mennini, T.10
Minetti, P.11
Di Cesare, M.A.12
Mastroianni, D.13
Scafetta, N.14
Galletti, B.15
Stasi, M.A.16
Castorina, M.17
Pacifici, L.18
Ghirardi, O.19
Tinti, O.20
Carminati, P.21
more..
-
27
-
-
9144232388
-
-
Campiani, G.; Butini, S.; Fattorusso, C.; Catalanotti, B.; Gemma, S.; Nacci, V.; Morelli, E.; Cagnotto, A.; Mereghetti, I.; Mennini, T.; Carli, M.; Minetti, P.; Di Cesare, M. A.; Mastroianni, D.; Scafetta, N.; Galletti, B.; Stasi, M. A.; Castorina, M.; Pacifici, L.; Vertechy, M.; Di Serio, S.; Ghirardi, O.; Tinti, O.; Carminati, P. Pyrrolo[1,3]benzothiazepine- based serotonin and dopamine receptor antagonists. Molecular modeling, further structure-activity relationship studies, and identification of novel atypical antipsychotic agents. J. Med. Chem. 2004, 47, 143-157.
-
(c) Campiani, G.; Butini, S.; Fattorusso, C.; Catalanotti, B.; Gemma, S.; Nacci, V.; Morelli, E.; Cagnotto, A.; Mereghetti, I.; Mennini, T.; Carli, M.; Minetti, P.; Di Cesare, M. A.; Mastroianni, D.; Scafetta, N.; Galletti, B.; Stasi, M. A.; Castorina, M.; Pacifici, L.; Vertechy, M.; Di Serio, S.; Ghirardi, O.; Tinti, O.; Carminati, P. Pyrrolo[1,3]benzothiazepine- based serotonin and dopamine receptor antagonists. Molecular modeling, further structure-activity relationship studies, and identification of novel atypical antipsychotic agents. J. Med. Chem. 2004, 47, 143-157.
-
-
-
-
28
-
-
20144377689
-
Novel atypical antipsychotic agents: Rational design, an efficient palladium-catalyzed route, and pharmacological studies
-
(d) Campiani, G.; Butini, S.; Fattorusso, C.; Trotta, F.; Gemma, S.; Catalanotti, B.; Nacci, V.; Fiorini, I.; Cagnotto, A.; Mereghetti, I.; Mennini, T.; Minetti, P.; Di Cesare, M. A.; Stasi, M. A.; Di Serio, S.; Ghirardi, O.; Tinti, O.; Carminati, P. Novel atypical antipsychotic agents: rational design, an efficient palladium-catalyzed route, and pharmacological studies. J. Med. Chem. 2005, 48, 1705-1708.
-
(2005)
J. Med. Chem
, vol.48
, pp. 1705-1708
-
-
Campiani, G.1
Butini, S.2
Fattorusso, C.3
Trotta, F.4
Gemma, S.5
Catalanotti, B.6
Nacci, V.7
Fiorini, I.8
Cagnotto, A.9
Mereghetti, I.10
Mennini, T.11
Minetti, P.12
Di Cesare, M.A.13
Stasi, M.A.14
Di Serio, S.15
Ghirardi, O.16
Tinti, O.17
Carminati, P.18
-
29
-
-
0042921579
-
2 receptors
-
2 receptors. J. Med. Chem. 2003, 46, 3822-3839.
-
(2003)
J. Med. Chem
, vol.46
, pp. 3822-3839
-
-
Campiani, G.1
Butini, S.2
Trotta, F.3
Fattorusso, C.4
Catalanotti, B.5
Aiello, F.6
Gemma, S.7
Nacci, V.8
Novellino, E.9
Stark, J.A.10
Cagnotto, A.11
Fumagalli, E.12
Carnovali, F.13
Cervo, L.14
Mennini, T.15
-
30
-
-
0033901262
-
Unexpected formation of quinolone derivatives in Reissert indole synthesis
-
Suzuki, H.; Gyoutoku, H.; Yokoo, H.; Shinba, M.; Sato, Y.; Yamada, H.; Murakami, Y. Unexpected formation of quinolone derivatives in Reissert indole synthesis. Synlett 2000, 8, 1196-1199.
-
(2000)
Synlett
, vol.8
, pp. 1196-1199
-
-
Suzuki, H.1
Gyoutoku, H.2
Yokoo, H.3
Shinba, M.4
Sato, Y.5
Yamada, H.6
Murakami, Y.7
-
31
-
-
0024806160
-
-
Rajur, S. B.; Merwade, A. Y.; Flendi, S. B.; Basanagoudar, I. D. Synthesis of 1,2,3,4-tetrahydropyrazino[1,2-a]indoles and ethyl 1-(2- amino-ethyl)indole-2-carboxylates. Indian J. Chem. 1989, 28B, 1065-1068.
-
Rajur, S. B.; Merwade, A. Y.; Flendi, S. B.; Basanagoudar, I. D. Synthesis of 1,2,3,4-tetrahydropyrazino[1,2-a]indoles and ethyl 1-(2- amino-ethyl)indole-2-carboxylates. Indian J. Chem. 1989, 28B, 1065-1068.
-
-
-
-
32
-
-
0020468430
-
-
Repke, D. B., III. Synthesis of 5-methoxy-and 5-hydroxy-1,2,3,4- tetrahydro-9H-pyrido[3,4-b]indoles. J. Heterocycl. Chem. 1982, 19, 845-848.
-
Repke, D. B., III. Synthesis of 5-methoxy-and 5-hydroxy-1,2,3,4- tetrahydro-9H-pyrido[3,4-b]indoles. J. Heterocycl. Chem. 1982, 19, 845-848.
-
-
-
-
33
-
-
0035006416
-
Application of phosphonium salts to the reactions of various kinds of amides
-
Sugimoto, O.; Mori, M.; Moriya, K.; Tanji, K. Application of phosphonium salts to the reactions of various kinds of amides. Helv. Chim. Acta 2001, 84, 1112-1118.
-
(2001)
Helv. Chim. Acta
, vol.84
, pp. 1112-1118
-
-
Sugimoto, O.1
Mori, M.2
Moriya, K.3
Tanji, K.4
-
34
-
-
0033550251
-
Synthesis of deuterium labelled desulfoglucosinolates as internal standards for LC-MS analysis
-
Robertson, A. A. B.; Botting, N. P. Synthesis of deuterium labelled desulfoglucosinolates as internal standards for LC-MS analysis. Tetrahedron 1999, 55, 13269-13284.
-
(1999)
Tetrahedron
, vol.55
, pp. 13269-13284
-
-
Robertson, A.A.B.1
Botting, N.P.2
-
35
-
-
64349117026
-
-
GPCR alignments;
-
GPCR alignments; www.bioinfo-pharma.u-strasbg.fr/gpcrdb/jss.html.
-
-
-
-
36
-
-
16844383383
-
The opsins
-
Terakita, A. The opsins. Genome Biol. 2005, 6, 213.
-
(2005)
Genome Biol
, vol.6
, pp. 213
-
-
Terakita, A.1
-
37
-
-
0032541084
-
G protein-coupled receptors. II. Mechanism of agonist activation
-
Gether, U.; Kobilka, B. K. G protein-coupled receptors. II. Mechanism of agonist activation. J. Biol. Chem. 1998, 273, 17979-17982.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 17979-17982
-
-
Gether, U.1
Kobilka, B.K.2
-
38
-
-
0035800850
-
Activation of the beta 2-adrenergic receptor involves disruption of an ionic lock between the cytoplasmic ends of transmembrane segments 3 and 6
-
Ballesteros, J. A.; Jensen, A. D.; Liapakis, G.; Rasmussen, S. G.; Shi, L.; Gether, U.; Javitch, J. A. Activation of the beta 2-adrenergic receptor involves disruption of an ionic lock between the cytoplasmic ends of transmembrane segments 3 and 6. J. Biol. Chem. 2001, 276, 29171-29177.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 29171-29177
-
-
Ballesteros, J.A.1
Jensen, A.D.2
Liapakis, G.3
Rasmussen, S.G.4
Shi, L.5
Gether, U.6
Javitch, J.A.7
-
39
-
-
0037192858
-
Evidence for a model of agonist-induced activation of 5-hy-droxytryptamine 2A serotonin receptors that involves the disruption of a strong ionic interaction between helices 3 and 6
-
Shapiro, D. A.; Kristiansen, K.; Weiner, D. M.; Kroeze, W. K.; Roth, B.L. Evidence for a model of agonist-induced activation of 5-hy-droxytryptamine 2A serotonin receptors that involves the disruption of a strong ionic interaction between helices 3 and 6. J. Biol. Chem. 2002, 277, 11441-11449.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 11441-11449
-
-
Shapiro, D.A.1
Kristiansen, K.2
Weiner, D.M.3
Kroeze, W.K.4
Roth, B.L.5
-
40
-
-
33144459843
-
Molecular mechanism of 7TM receptor activation-a global toggle switch model
-
Schwartz, T. W.; Frimurer, T. M.; Holst, B.; Rosenkilde, M. M.; Elling, C.E. Molecular mechanism of 7TM receptor activation-a global toggle switch model. Annu. Rev. Pharmacol. Toxicol. 2006, 46, 481-519.
-
(2006)
Annu. Rev. Pharmacol. Toxicol
, vol.46
, pp. 481-519
-
-
Schwartz, T.W.1
Frimurer, T.M.2
Holst, B.3
Rosenkilde, M.M.4
Elling, C.E.5
-
41
-
-
0036169280
-
The binding site of aminergic G protein-coupled receptors: The transmembrane segments and second extracellular loop
-
Shi, L.; Javitch, J. A. The binding site of aminergic G protein-coupled receptors: the transmembrane segments and second extracellular loop. Annu. Rev. Pharmacol. Toxicol. 2002, 42, 437-467.
-
(2002)
Annu. Rev. Pharmacol. Toxicol
, vol.42
, pp. 437-467
-
-
Shi, L.1
Javitch, J.A.2
-
42
-
-
0032570306
-
A cluster of aromatic residues in the sixth membrane-spanning segment of the dopamine D2 receptor is accessible in the binding-site crevice
-
Javitch, J. A.; Ballesteros, J. A.; Weinstein, H.; Chen, J. A cluster of aromatic residues in the sixth membrane-spanning segment of the dopamine D2 receptor is accessible in the binding-site crevice. Biochemistry 1998, 37, 998-1006.
-
(1998)
Biochemistry
, vol.37
, pp. 998-1006
-
-
Javitch, J.A.1
Ballesteros, J.A.2
Weinstein, H.3
Chen, J.4
-
43
-
-
36248970132
-
Crystal structure of the human beta2 adrenergic G-protein-coupled receptor
-
Rasmussen, S. G.; Choi, H. J.; Rosenbaum, D. M.; Kobilka, T. S.; Thian, F. S.; Edwards, P. C.; Burghammer, M.; Ratnala, V. R.; Sanishvili, R.; Fischetti, R. F.; Schertler, G. F.; Weis, W. I.; Kobilka, B. K. Crystal structure of the human beta2 adrenergic G-protein-coupled receptor. Nature 2007, 450, 383-387.
-
(2007)
Nature
, vol.450
, pp. 383-387
-
-
Rasmussen, S.G.1
Choi, H.J.2
Rosenbaum, D.M.3
Kobilka, T.S.4
Thian, F.S.5
Edwards, P.C.6
Burghammer, M.7
Ratnala, V.R.8
Sanishvili, R.9
Fischetti, R.F.10
Schertler, G.F.11
Weis, W.I.12
Kobilka, B.K.13
-
44
-
-
36448995359
-
High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor
-
Cherezov, V.; Rosenbaum, D. M.; Hanson, M. A.; Rasmussen, S. G.; Thian, F. S.; Kobilka, T. S.; Choi, H. J.; Kuhn, P.; Weis, W. I.; Kobilka, B. K.; Stevens, R. C. High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor. Science 2007, 318, 1258-1265.
-
(2007)
Science
, vol.318
, pp. 1258-1265
-
-
Cherezov, V.1
Rosenbaum, D.M.2
Hanson, M.A.3
Rasmussen, S.G.4
Thian, F.S.5
Kobilka, T.S.6
Choi, H.J.7
Kuhn, P.8
Weis, W.I.9
Kobilka, B.K.10
Stevens, R.C.11
-
45
-
-
36448978229
-
GPCR engineering yields high- resolution structural insights into beta2-adrenergic receptor function
-
Rosenbaum, D. M.; Cherezov, V.; Hanson, M. A.; Rasmussen, S. G.; Thian, F. S.; Kobilka, T. S.; Choi, H. J.; Yao, X. J.; Weis, W. I.; Stevens, R. C.; Kobilka, B. K. GPCR engineering yields high- resolution structural insights into beta2-adrenergic receptor function. Science 2007, 318, 1266-1273.
-
(2007)
Science
, vol.318
, pp. 1266-1273
-
-
Rosenbaum, D.M.1
Cherezov, V.2
Hanson, M.A.3
Rasmussen, S.G.4
Thian, F.S.5
Kobilka, T.S.6
Choi, H.J.7
Yao, X.J.8
Weis, W.I.9
Stevens, R.C.10
Kobilka, B.K.11
-
46
-
-
1642410853
-
-
Kalani, M. Y.; Vaidehi, N.; Hall, S. E.; Trabanino, R. J.; Freddolino, P. L.; Kalani, M. A.; Floriano, W. B.; Kam, V. W.; Goddard, W. A., 3rd. The predicted 3D structure of the human D2 dopamine receptor and the binding site and binding affinities for agonists and antagonists. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 3815-3820.
-
Kalani, M. Y.; Vaidehi, N.; Hall, S. E.; Trabanino, R. J.; Freddolino, P. L.; Kalani, M. A.; Floriano, W. B.; Kam, V. W.; Goddard, W. A., 3rd. The predicted 3D structure of the human D2 dopamine receptor and the binding site and binding affinities for agonists and antagonists. Proc. Natl. Acad. Sci. U.S.A. 2004, 101, 3815-3820.
-
-
-
-
47
-
-
0030742276
-
Identification of conserved aromatic residues essential for agonist binding and second messenger production at 5-hydroxytryptamine2A receptors
-
Roth, B. L.; Shoham, M.; Choudhary, M. S.; Khan, N. Identification of conserved aromatic residues essential for agonist binding and second messenger production at 5-hydroxytryptamine2A receptors. Mol. Pharmacol. 1997, 52, 259-266.
-
(1997)
Mol. Pharmacol
, vol.52
, pp. 259-266
-
-
Roth, B.L.1
Shoham, M.2
Choudhary, M.S.3
Khan, N.4
-
48
-
-
33748032418
-
3 receptor ligands: Structure-activity relationships and selected neu- ropharmacological aspects
-
3 receptor ligands: structure-activity relationships and selected neu- ropharmacological aspects. Pharmacol Ther. 2006, 112, 281-333.
-
(2006)
Pharmacol Ther
, vol.112
, pp. 281-333
-
-
Boeckler, F.1
Gmeiner, P.2
-
49
-
-
0030880426
-
Interaction of tryptamine and ergoline compounds with threonine 196 in the ligand binding site of the 5-hydroxytryptamine6 receptor
-
Boess, F. G., Jr.; Meyer, V.; Zwingelstein, C.; Sleight, A. J. Interaction of tryptamine and ergoline compounds with threonine 196 in the ligand binding site of the 5-hydroxytryptamine6 receptor. Mol. Pharmacol. 1997, 52, 515-523.
-
(1997)
Mol. Pharmacol
, vol.52
, pp. 515-523
-
-
Boess Jr., F.G.1
Meyer, V.2
Zwingelstein, C.3
Sleight, A.J.4
-
50
-
-
0033786003
-
Differential modes of agonist binding to 5-hydroxytryptamine(2A) serotonin receptors revealed by mutation and molecular modeling of conserved residues in transmembrane region 5
-
Shapiro, D. A.; Kristiansen, K.; Kroeze, W. K.; Roth, B. L. Differential modes of agonist binding to 5-hydroxytryptamine(2A) serotonin receptors revealed by mutation and molecular modeling of conserved residues in transmembrane region 5. Mol. Pharmacol. 2000, 58, 877-886.
-
(2000)
Mol. Pharmacol
, vol.58
, pp. 877-886
-
-
Shapiro, D.A.1
Kristiansen, K.2
Kroeze, W.K.3
Roth, B.L.4
-
51
-
-
0028009827
-
Species variations in transmembrane region V of the 5-hydroxytryptamine type 2A receptor alter the structure-activity relationship of certain ergolines and tryptamines
-
Johnson, M. P.; Loncharich, R. J.; Baez, M.; Nelson, D. L. Species variations in transmembrane region V of the 5-hydroxytryptamine type 2A receptor alter the structure-activity relationship of certain ergolines and tryptamines. Mol. Pharmacol. 1994, 45, 277-286.
-
(1994)
Mol. Pharmacol
, vol.45
, pp. 277-286
-
-
Johnson, M.P.1
Loncharich, R.J.2
Baez, M.3
Nelson, D.L.4
-
53
-
-
47249159421
-
Modeling hERG and its Interactions with Drugs: Recent Advances in Light of Current Potassium Channel Simulations
-
Recanatini, M.; Cavalli, A.; Masetti, M. Modeling hERG and its Interactions with Drugs: Recent Advances in Light of Current Potassium Channel Simulations. ChemMedChem. 2008, 3, 523-535.
-
(2008)
ChemMedChem
, vol.3
, pp. 523-535
-
-
Recanatini, M.1
Cavalli, A.2
Masetti, M.3
-
54
-
-
34250836484
-
Drug block of the hERG potassium channel: Insight from modelling
-
Stansfeld, P. J.; Gedeck, P.; Gosling, M.; Cox, B.; Mitcheson, J. S.; Sutcliffe, M. J. Drug block of the hERG potassium channel: insight from modelling. Proteins 2007, 68, 568-580.
-
(2007)
Proteins
, vol.68
, pp. 568-580
-
-
Stansfeld, P.J.1
Gedeck, P.2
Gosling, M.3
Cox, B.4
Mitcheson, J.S.5
Sutcliffe, M.J.6
-
55
-
-
33644967111
-
New insights about hERG blockade obtained from protein modeling, potential energy mapping, and docking studies
-
Farid, R.; Day, T.; Friesner, R. A.; Pearlstein, R. A. New insights about hERG blockade obtained from protein modeling, potential energy mapping, and docking studies. Bioorg. Med. Chem. 2006, 14, 3160-3173.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 3160-3173
-
-
Farid, R.1
Day, T.2
Friesner, R.A.3
Pearlstein, R.A.4
-
56
-
-
33645816995
-
Molecular determinants of hERG channel block
-
Kamiya, K.; Niwa, R.; Mitcheson, J. S.; Sanguinetti, M. C. Molecular determinants of hERG channel block. Mol. Pharmacol. 2006, 69, 1709-1716.
-
(2006)
Mol. Pharmacol
, vol.69
, pp. 1709-1716
-
-
Kamiya, K.1
Niwa, R.2
Mitcheson, J.S.3
Sanguinetti, M.C.4
-
57
-
-
44249086160
-
Topological mapping of the asymmetric drug binding to the human ether-à-go-go-related gene product (hERG) potassium channel by use of tandem dimers
-
Myokai, T.; Ryu, S.; Shimizu, H.; Oiki, S. Topological mapping of the asymmetric drug binding to the human ether-à-go-go-related gene product (hERG) potassium channel by use of tandem dimers. Mol. Pharmacol. 2008, 73, 1643-1651.
-
(2008)
Mol. Pharmacol
, vol.73
, pp. 1643-1651
-
-
Myokai, T.1
Ryu, S.2
Shimizu, H.3
Oiki, S.4
-
58
-
-
0038743107
-
Characterization of hERG potassium channel inhibition using CoMSiA 3D QSAR and homology modeling approaches
-
Pearlstein, R. A.; Vaz, R. J.; Kang, J.; Chen, X. L.; Preobrazhenskaya, M.; Shchekotikhin, A. E.; Korolev, A. M.; Lysenkova, L. N.; Miroshnikova, O. V.; Hendrix, J.; Rampe, D. Characterization of hERG potassium channel inhibition using CoMSiA 3D QSAR and homology modeling approaches. Bioorg. Med. Chem. Lett. 2003,13, 1829-1835.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 1829-1835
-
-
Pearlstein, R.A.1
Vaz, R.J.2
Kang, J.3
Chen, X.L.4
Preobrazhenskaya, M.5
Shchekotikhin, A.E.6
Korolev, A.M.7
Lysenkova, L.N.8
Miroshnikova, O.V.9
Hendrix, J.10
Rampe, D.11
-
59
-
-
0037194634
-
Toward a pharmacophore for drugs inducing the long QT syndrome: Insights from a CoMFA study of hERG K(+) channel blockers
-
Cavalli, A.; Poluzzi, E.; De Ponti, F.; Recanatini, M. Toward a pharmacophore for drugs inducing the long QT syndrome: insights from a CoMFA study of hERG K(+) channel blockers. J. Med. Chem. 2002, 45, 3844-3853.
-
(2002)
J. Med. Chem
, vol.45
, pp. 3844-3853
-
-
Cavalli, A.1
Poluzzi, E.2
De Ponti, F.3
Recanatini, M.4
-
60
-
-
0035096016
-
1a receptor activation: A possible mechanism of atypical antipsychotic-induced cortical dopamine release
-
1a receptor activation: a possible mechanism of atypical antipsychotic-induced cortical dopamine release. J. Neuro- chem. 2001, 76, 1521-1531.
-
(2001)
J. Neuro- chem
, vol.76
, pp. 1521-1531
-
-
Ichikawa, J.1
Ishii, H.2
Bonaccorso, S.3
Fowler, W.L.4
O'Laughlin, I.A.5
Meltzer, H.Y.6
-
62
-
-
0031023562
-
Blockade of phencyclidine-induced hyperlocomotion by olanzapine, clozapine and serotonin receptor subtype selective antagonists in mice
-
(b) Gleason, S. D.; Shannon, H. E. Blockade of phencyclidine-induced hyperlocomotion by olanzapine, clozapine and serotonin receptor subtype selective antagonists in mice. Psychopharmacology (Berlin) 1997, 129, 79-84.
-
(1997)
Psychopharmacology (Berlin)
, vol.129
, pp. 79-84
-
-
Gleason, S.D.1
Shannon, H.E.2
-
63
-
-
0026775521
-
-
Deutch, A. Y.; Lee, M. C.; Iadarola, M. J. Regionally specific effects of atypical antipsychotic drugs on striatal fos expression: the nucleus accumbens shell as a locus of antipsychotic action. Mol. Cell. Neurosci. 1992, 3, 332-341. (b) Robertson, G. S.; Fibiger, H. C. Neuroleptics increase c-fos expression in the forebrain: contrasting effects of haloperidol and clozapine. Neuroscience 1992, 46, 315-328.
-
(a) Deutch, A. Y.; Lee, M. C.; Iadarola, M. J. Regionally specific effects of atypical antipsychotic drugs on striatal fos expression: the nucleus accumbens shell as a locus of antipsychotic action. Mol. Cell. Neurosci. 1992, 3, 332-341. (b) Robertson, G. S.; Fibiger, H. C. Neuroleptics increase c-fos expression in the forebrain: contrasting effects of haloperidol and clozapine. Neuroscience 1992, 46, 315-328.
-
-
-
-
64
-
-
0032466201
-
Modification of haloperidol- induced pattern of c-fos expression by serotonin agonists
-
Tremblay, P. O.; Gervais, J.; Rouillard, C. Modification of haloperidol- induced pattern of c-fos expression by serotonin agonists. Eur. J. Neurosci. 1998, 10, 3546-3555.
-
(1998)
Eur. J. Neurosci
, vol.10
, pp. 3546-3555
-
-
Tremblay, P.O.1
Gervais, J.2
Rouillard, C.3
-
65
-
-
0028135046
-
Induction Patterns of Fos-Like Immunoreactivity in the Forebrain as Predictors of Atypical Antipsychotic Activity
-
Robertson, G. S.; Matsumura, H.; Fibiger, H. C. Induction Patterns of Fos-Like Immunoreactivity in the Forebrain as Predictors of Atypical Antipsychotic Activity. J Pharmacol Exp Ther. 1994, 271, 1058-1066.
-
(1994)
J Pharmacol Exp Ther
, vol.271
, pp. 1058-1066
-
-
Robertson, G.S.1
Matsumura, H.2
Fibiger, H.C.3
-
66
-
-
1042277046
-
Testing the validity of c-fos expression profiling to aid the therapeutic classification of psychoactive drugs
-
Sumner, B. E.; Cruise, L. A.; Slattery, D. A.; Hill, D. R.; Shahid, M.; Henry, B. Testing the validity of c-fos expression profiling to aid the therapeutic classification of psychoactive drugs. Psychopharmacology (Berlin) 2004, 171, 306-321.
-
(2004)
Psychopharmacology (Berlin)
, vol.171
, pp. 306-321
-
-
Sumner, B.E.1
Cruise, L.A.2
Slattery, D.A.3
Hill, D.R.4
Shahid, M.5
Henry, B.6
-
67
-
-
0033550212
-
Synthesis of meta-substituted aniline derivatives by nucleophilic substitution
-
Belfield, A. J.; Brown, G. R.; Foubister, A. J.; Ratcliffe, P. D. Synthesis of meta-substituted aniline derivatives by nucleophilic substitution. Tetrahedron 1999, 55, 13285-13300.
-
(1999)
Tetrahedron
, vol.55
, pp. 13285-13300
-
-
Belfield, A.J.1
Brown, G.R.2
Foubister, A.J.3
Ratcliffe, P.D.4
-
68
-
-
44949229187
-
Exploiting Protein Fluctuations at the Active-Site Gorge of Human Cholinesterases: Further Optimization of the Design Strategy to Develop Extremely Potent Inhibitors
-
Butini, S.; Campiani, G.; Borriello, M.; Gemma, S.; Panico, A.; Persico, M.; Catalanotti, B.; Ros, S.; Brindisi, M.; Agnusdei, M.; Fiorini, I.; Nacci, V.; Novellino, E.; Belinskaya, T.; Saxena, A.; Fattorusso, C. Exploiting Protein Fluctuations at the Active-Site Gorge of Human Cholinesterases: Further Optimization of the Design Strategy to Develop Extremely Potent Inhibitors. J. Med. Chem. 2008, 51, 3154-3170.
-
(2008)
J. Med. Chem
, vol.51
, pp. 3154-3170
-
-
Butini, S.1
Campiani, G.2
Borriello, M.3
Gemma, S.4
Panico, A.5
Persico, M.6
Catalanotti, B.7
Ros, S.8
Brindisi, M.9
Agnusdei, M.10
Fiorini, I.11
Nacci, V.12
Novellino, E.13
Belinskaya, T.14
Saxena, A.15
Fattorusso, C.16
-
69
-
-
5244247401
-
A III atomic level simulations on a million particles: The cell multipole method for Coulomb and London nonbond interactions
-
Ding, H. Q.; Karasawa, N.; Goddard, W. A III atomic level simulations on a million particles: the cell multipole method for Coulomb and London nonbond interactions. J. Chem. Phys. 1992, 97, 4309-4315.
-
(1992)
J. Chem. Phys
, vol.97
, pp. 4309-4315
-
-
Ding, H.Q.1
Karasawa, N.2
Goddard, W.3
-
70
-
-
0023769808
-
Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system
-
Dauber-Osguthorpe, P.; Roberts, V. A.; Osguthorpe, D. J.; Wolff, J.; Genest, M.; Hagler, A. T. Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system. Proteins 1988, 4, 31-47.
-
(1988)
Proteins
, vol.4
, pp. 31-47
-
-
Dauber-Osguthorpe, P.1
Roberts, V.A.2
Osguthorpe, D.J.3
Wolff, J.4
Genest, M.5
Hagler, A.T.6
-
71
-
-
84986527718
-
Derivation of class II force fields. I. Methodology and quantum force field for the alkyl functional group and alkane molecules
-
Maple, J. R.; Hwang, M. J.; Stockfisch, T. P.; Dinur, U.; Waldman, M.; Ewig, C. S.; Hagler, A. T. Derivation of class II force fields. I. Methodology and quantum force field for the alkyl functional group and alkane molecules. J Comput Chem. 1994, 15, 162-182.
-
(1994)
J Comput Chem
, vol.15
, pp. 162-182
-
-
Maple, J.R.1
Hwang, M.J.2
Stockfisch, T.P.3
Dinur, U.4
Waldman, M.5
Ewig, C.S.6
Hagler, A.T.7
-
74
-
-
0018001339
-
Simultaneous analysis of families of sigmoidal curves: Application to bioassay, radioligand assay and physiological dose-response curves
-
DeLean, K. W.; Munson, P. J.; Rodbard, D. Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay and physiological dose-response curves. Am. J. Physiol. 1978, 235, E97-E102.
-
(1978)
Am. J. Physiol
, vol.235
-
-
DeLean, K.W.1
Munson, P.J.2
Rodbard, D.3
-
76
-
-
34249804470
-
Alpha-7 nicotinic acetylcholine receptor agonists selectively activate limbic regions of the rat forebrain: An effect similar to antipsychotics
-
Hansen, H. H.; Timmermann, D. B.; Peters, D.; Walters, C.; Damaj, M. I.; Mikkelsen, J. D. Alpha-7 nicotinic acetylcholine receptor agonists selectively activate limbic regions of the rat forebrain: an effect similar to antipsychotics. J. Neurosci. Res. 2007, 85, 1810-1818.
-
(2007)
J. Neurosci. Res
, vol.85
, pp. 1810-1818
-
-
Hansen, H.H.1
Timmermann, D.B.2
Peters, D.3
Walters, C.4
Damaj, M.I.5
Mikkelsen, J.D.6
-
77
-
-
0032214969
-
Expression of Fos in the circadian system following nonphotic stimulation
-
Mikkelsen, J. D.; Vrang, N.; Mrosovsky, N. Expression of Fos in the circadian system following nonphotic stimulation. Brain Res. Bull. 1998, 47, 367-376.
-
(1998)
Brain Res. Bull
, vol.47
, pp. 367-376
-
-
Mikkelsen, J.D.1
Vrang, N.2
Mrosovsky, N.3
|