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The dopamine D3-receptor : a postsynaptic receptor inhibitory on rat locomotor activity

Journal of Neural Transmission, 1993-01, Vol.94 (1), p.11-19

1993

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Common discriminative stimulus properties in rats of muscarinic antagonists, clozapine and the D 3 preferring antagonist PNU-99194A: an analysis of possible mechanisms

Behavioural pharmacology, 2001-09, Vol.12 (5), p.303-315

2001

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Common discriminative stimulus properties in rats of muscarinic antagonists, clozapine and the D3 preferring antagonist PNU-99194a: an analysis of possible mechanisms

Behavioural pharmacology, 2001-09, Vol.12 (5), p.303-315

2001

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Differential effects of dopamine D2 and D3 receptor antagonists in regard to dopamine release, in vivo receptor displacement and behaviour

Journal of Neural Transmission, 1994-01, Vol.98 (1), p.39-55

1994

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Comparison of 5-HT1A and dopamine D2 pharmacophores. X-ray structures and affinities of conformationally constrained ligands

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1301-1315

1993

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C-9 and N-Substituted Analogs of cis-(3aR)-(-)-2,3,3a,4,5,9b-Hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: 5-HT1A Receptor Agonists with Various Degrees of Metabolic Stability

Journal of medicinal chemistry, 1995-02, Vol.38 (4), p.725-734

1995

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Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted 2-Aminoindans

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4716-4732

2001

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Synthesis and biological activity of cis-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: A potent and selective 5-HT1A receptor agonist with good oral availability

Journal of medicinal chemistry, 1993-07, Vol.36 (15), p.2208-2218

1993

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Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

Journal of medicinal chemistry, 1993-03, Vol.36 (6), p.671-682

1993

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The chemical structure of U99194A

Journal of neural transmission. General section, 1995, Vol.99 (1-3), p.I

1995

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ChemInform Abstract: Synthesis of (R)- and (S)-1-Formyl-6,7,8,9-tetrahydro-N,N-(dipropyl)- 3H-benz(e)indol-8-amines: Potent and Orally Active 5-HT1A Receptor Agonists

ChemInform, 1995-03, Vol.26 (11), p.no-no

1995

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ChemInform Abstract: Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H- benz(e)indole Ring System. Part 2. Effect of 8-Amino Nitrogen Substitution on Serotonin Receptor Binding and Pharmacology

ChemInform, 1995-10, Vol.26 (42), p.no-no

1995

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Centrally acting serotonergic and dopaminergic agents. 2. Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Journal of medicinal chemistry, 1993-04, Vol.36 (8), p.1069-1083

1993

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ChemInform Abstract: Synthesis and Biological Activity of cis-(3aR)-(-)-2,3,3a,4,5,9b- Hexahydro-3-propyl-1H-benz(e)indole-9-carboxami de (VII): A Potent and Selective 5-HT1A Receptor Agonist with Good Oral Availability

ChemInform, 1994-11, Vol.25 (45), p.no-no

1994

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Centrally acting serotonergic and dopaminergic agents. 1. Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Journal of medicinal chemistry, 1993-04, Vol.36 (8), p.1053-1068

1993

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Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232 : increased dopamine D3 receptor preference and improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 1994-03, Vol.4 (5), p.689-694

1994

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Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist

Journal of labelled compounds & radiopharmaceuticals, 1997-11, Vol.39 (11), p.891-900

1997

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Dopamine D(3) receptor antagonists. 1. Synthesis and structure-activity relationships of 5,6-dimethoxy-N-alkyl- and N-alkylaryl-substituted 2-aminoindans

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4716-4732

2001

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Synthesis of (r)- and (s)-1-formyl-6,7,8,9-tetrahydro- N,N-(dipropyl)-3H-benz[e]indol-8-amines: Potent and orally active 5-ht1a receptor agonists

Journal of heterocyclic chemistry, 1994-01, Vol.31 (1), p.129-139

1994

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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effect of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2217-2230

1995

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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2217-2230

1995

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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. II: Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Journal of medicinal chemistry, 1995, Vol.38 (12), p.2217-2230

1995

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Centrally acting serotonergic and dopaminergic agents. II: Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Journal of medicinal chemistry, 1993, Vol.36 (8), p.1069-1083

1993

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Centrally acting serotonergic and dopaminergic agents. I: Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Journal of medicinal chemistry, 1993, Vol.36 (8), p.1053-1068

1993

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Dopamine D 3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy- N -alkyl- and N -Alkylaryl-Substituted 2-Aminoindans

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4716-4732

2001

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The dopamine D3-receptor : a postsynaptic receptor inhibitory on rat locomotor activity

Common discriminative stimulus properties in rats of muscarinic antagonists, clozapine and the D 3 preferring antagonist PNU-99194A: an analysis of possible mechanisms

Common discriminative stimulus properties in rats of muscarinic antagonists, clozapine and the D3 preferring antagonist PNU-99194a: an analysis of possible mechanisms

Differential effects of dopamine D2 and D3 receptor antagonists in regard to dopamine release, in vivo receptor displacement and behaviour

Comparison of 5-HT1A and dopamine D2 pharmacophores. X-ray structures and affinities of conformationally constrained ligands

C-9 and N-Substituted Analogs of cis-(3aR)-(-)-2,3,3a,4,5,9b-Hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: 5-HT1A Receptor Agonists with Various Degrees of Metabolic Stability

Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted 2-Aminoindans

Synthesis and biological activity of cis-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-propyl-1H-benz[e]indole-9-carboxamide: A potent and selective 5-HT1A receptor agonist with good oral availability

Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

The chemical structure of U99194A

ChemInform Abstract: Synthesis of (R)- and (S)-1-Formyl-6,7,8,9-tetrahydro-N,N-(dipropyl)- 3H-benz(e)indol-8-amines: Potent and Orally Active 5-HT1A Receptor Agonists

ChemInform Abstract: Structure-Activity Relationships in the 8-Amino-6,7,8,9-tetrahydro-3H- benz(e)indole Ring System. Part 2. Effect of 8-Amino Nitrogen Substitution on Serotonin Receptor Binding and Pharmacology

Centrally acting serotonergic and dopaminergic agents. 2. Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

ChemInform Abstract: Synthesis and Biological Activity of cis-(3aR)-(-)-2,3,3a,4,5,9b- Hexahydro-3-propyl-1H-benz(e)indole-9-carboxami de (VII): A Potent and Selective 5-HT1A Receptor Agonist with Good Oral Availability

Centrally acting serotonergic and dopaminergic agents. 1. Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Synthesis and biological activity of C-5 modified derivatives of (+)-AJ76 and (+)-UH232 : increased dopamine D3 receptor preference and improved pharmacokinetic properties

Synthesis of isotopically labeled CIS-(3aR)-(-)-2,3,3a,4,5,9b-hexahydro-3-(N-propyl)-1H-benz[e]indole-9-carboxamide, a 5-HT1A receptor agonist

Dopamine D(3) receptor antagonists. 1. Synthesis and structure-activity relationships of 5,6-dimethoxy-N-alkyl- and N-alkylaryl-substituted 2-aminoindans

Synthesis of (r)- and (s)-1-formyl-6,7,8,9-tetrahydro- N,N-(dipropyl)-3H-benz[e]indol-8-amines: Potent and orally active 5-ht1a receptor agonists

Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effect of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. II: Effects of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology

Centrally acting serotonergic and dopaminergic agents. II: Synthesis and structure-activity relationships of 2,3,3a,4,9,9a-hexahydro-1H-benz[f]indole derivatives

Centrally acting serotonergic and dopaminergic agents. I: Synthesis and structure-activity relationships of 2,3,3a,4,5,9b-hexahydro-1H-benz[e]indole derivatives

Dopamine D 3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy- N -alkyl- and N -Alkylaryl-Substituted 2-Aminoindans

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