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Optimization of isochromanone based urotensin II receptor agonists

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (13), p.4844-4854

2010

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Identification of novel subtype selective RAR agonists

Biochemical pharmacology, 2005-12, Vol.71 (1), p.156-162

2005

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Pimavanserin, a selective serotonin (5-HT)2A-inverse agonist, enhances the efficacy and safety of risperidone, 2 mg/day, but does not enhance efficacy of haloperidol, 2 mg/day: Comparison with reference dose risperidone, 6 mg/day

Schizophrenia research, 2012-11, Vol.141 (2), p.144-152

2012

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Pimavanserin, a selective serotonin (5-HT)2A-inverse agonist, enhances the efficacy and safety of risperidone, 2mg/day, but does not enhance efficacy of haloperidol, 2mg/day: Comparison with reference dose risperidone, 6mg/day

Schizophrenia research, 2012-11, Vol.141 (2-3), p.144-152

2012

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Design, parallel synthesis and SAR of novel urotensin II receptor agonists

European journal of medicinal chemistry, 2007-02, Vol.42 (2), p.276-285

2007

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Isochromanone-based urotensin-II receptor agonists

Bioorganic & medicinal chemistry, 2005-04, Vol.13 (8), p.3057-3068

2005

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Novel and potent small-molecule urotensin II receptor agonists

Bioorganic & medicinal chemistry, 2009-07, Vol.17 (13), p.4657-4665

2009

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(R)- and (S)-8-acetyl-2-(dipropylamino)tetralin (LY-41) : two novel 5-HT1A receptor agonists

European journal of pharmacology, 1993-01, Vol.231 (1), p.69-76

1993

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Pharmacology of polymorphic variants of the human 5-HT1A receptor

Biochemical pharmacology, 2004-02, Vol.67 (3), p.479-490

2004

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Pharmacology of polymorphic variants of the human 5-HT 1A receptor

Biochemical pharmacology, 2004, Vol.67 (3), p.479-490

2004

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Interactions of ligands with active and inactive conformations of the dopamine D 2 receptor

European journal of pharmacology, 1998-04, Vol.346 (2), p.299-307

1998

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Derivatives of 2-arylcyclopropylamine: Synthesis and interactions with 5-HT 1A receptors

Bioorganic & medicinal chemistry letters, 1996, Vol.6 (4), p.415-420

1996

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Interactions of ligands with active and inactive conformations of the dopamine D2 receptor

European journal of pharmacology, 1998-04, Vol.346 (2-3), p.299-307

1998

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Differential serotoninergic and dopaminergic activities of the (R) - and the (S) -enantiomers of 2-(di-n-propylamino) tetralin

European journal of pharmacology, 1996-05, Vol.303 (3), p.151-162

1996

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Stereoselective palladium-catalyzed cyclopropanation of α,β-unsaturated carboxylic acids derivatized with oppolzer's sultam

Tetrahedron letters, 1991-09, Vol.32 (40), p.5625-5628

1991

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3-Lithioquinuclidin-2-ene: A novel intermediate for the synthesis of muscarinic agonists and antagonists

Bioorganic & medicinal chemistry letters, 1994-12, Vol.4 (24), p.2837-2840

1994

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Chirality in drug research and design

Trends in biotechnology, 1993-03, Vol.11 (3), p.73-74

1993

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Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT 1A and D 2A receptors

Bioorganic & medicinal chemistry letters, 1999, Vol.9 (11), p.1583-1586

1999

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Palladium catalyzed syntheses of phenyl-substittuted pgf2α analogues: potential antigluaucoma agents

Bioorganic & medicinal chemistry letters, 1993-02, Vol.3 (2), p.241-244

1993

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Ligand-controlled palladium-catalyzed intramolecular reactions of phenyl-substituted prostaglandin F2 α analogues

Tetrahedron, 1995-08, Vol.51 (33), p.9139-9154

1995

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Derivatives of 2-arylcyclopropylamine: Synthesis and interactions with 5-HT1A receptors

Bioorganic & medicinal chemistry letters, 1996-02, Vol.6 (4), p.415-420

1996

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(S)-UH-301 antagonizes (R)-8-OH-DPAT-indiiced cardiovascular effects in the rat

European journal of pharmacology, 1991-07, Vol.199 (3), p.367-370

1991

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Palladium catalyzed syntheses of phenyl-substittuted pgf 2α analogues: potential antigluaucoma agents

Bioorganic & medicinal chemistry letters, 1993, Vol.3 (2), p.241-244

1993

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Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT1A and D2A receptors

Bioorganic & medicinal chemistry letters, 1999-06, Vol.9 (11), p.1583-1586

1999

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Novel L-Phe-Gly mimetics

Tetrahedron letters, 1992-07, Vol.33 (31), p.4487-4490

1992

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Optimization of isochromanone based urotensin II receptor agonists

Identification of novel subtype selective RAR agonists

Pimavanserin, a selective serotonin (5-HT)2A-inverse agonist, enhances the efficacy and safety of risperidone, 2 mg/day, but does not enhance efficacy of haloperidol, 2 mg/day: Comparison with reference dose risperidone, 6 mg/day

Pimavanserin, a selective serotonin (5-HT)2A-inverse agonist, enhances the efficacy and safety of risperidone, 2mg/day, but does not enhance efficacy of haloperidol, 2mg/day: Comparison with reference dose risperidone, 6mg/day

Design, parallel synthesis and SAR of novel urotensin II receptor agonists

Isochromanone-based urotensin-II receptor agonists

Novel and potent small-molecule urotensin II receptor agonists

(R)- and (S)-8-acetyl-2-(dipropylamino)tetralin (LY-41) : two novel 5-HT1A receptor agonists

Pharmacology of polymorphic variants of the human 5-HT1A receptor

Pharmacology of polymorphic variants of the human 5-HT 1A receptor

Interactions of ligands with active and inactive conformations of the dopamine D 2 receptor

Derivatives of 2-arylcyclopropylamine: Synthesis and interactions with 5-HT 1A receptors

Interactions of ligands with active and inactive conformations of the dopamine D2 receptor

Differential serotoninergic and dopaminergic activities of the (R) - and the (S) -enantiomers of 2-(di-n-propylamino) tetralin

Stereoselective palladium-catalyzed cyclopropanation of α,β-unsaturated carboxylic acids derivatized with oppolzer's sultam

3-Lithioquinuclidin-2-ene: A novel intermediate for the synthesis of muscarinic agonists and antagonists

Chirality in drug research and design

Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT 1A and D 2A receptors

Palladium catalyzed syntheses of phenyl-substittuted pgf2α analogues: potential antigluaucoma agents

Ligand-controlled palladium-catalyzed intramolecular reactions of phenyl-substituted prostaglandin F2 α analogues

Derivatives of 2-arylcyclopropylamine: Synthesis and interactions with 5-HT1A receptors

(S)-UH-301 antagonizes (R)-8-OH-DPAT-indiiced cardiovascular effects in the rat

Palladium catalyzed syntheses of phenyl-substittuted pgf 2α analogues: potential antigluaucoma agents

Novel derivatives of 3-(dipropylamino)chroman. Interactions with 5-HT1A and D2A receptors

Novel L-Phe-Gly mimetics

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