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The anxiolytic-like effects of the novel, orally active nociceptin opioid receptor agonist 8-[bis(2-methylphenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octan-3-ol (SCH 221510)

The Journal of pharmacology and experimental therapeutics, 2008-08, Vol.326 (2), p.672-682

2008

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Cyclic urea derivatives as potent NK1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (4), p.1065-1069

2006

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Interdisciplinary Teaching of Pharmacology and Genetics: Comparing Two Different Active Learning Models in Medical School

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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The Gerbil Elevated Plus-maze II: Anxiolytic-like Effects of Selective Neurokinin NK1 Receptor Antagonists

Neuropsychopharmacology (New York, N.Y.), 2002-09, Vol.27 (3), p.371-379

2002

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The Gerbil Elevated Plus-Maze I: Behavioral Characterization and Pharmacological Validation

Neuropsychopharmacology (New York, N.Y.), 2002-09, Vol.27 (3), p.357-370

2002

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Cyclic urea derivatives as potent NK1 selective antagonists

Bioorganic & medicinal chemistry letters, 2005-09, Vol.15 (17), p.3896-3899

2005

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SCH 57790, a selective muscarinic M2 receptor antagonist, releases acetylcholine and produces cognitive enhancement in laboratory animals

European journal of pharmacology, 2001-11, Vol.431 (2), p.189-200

2001

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Improving the Oral Efficacy of CNS Drug Candidates: Discovery of Highly Orally Efficacious Piperidinyl Piperidine M2 Muscarinic Receptor Antagonists

Journal of medicinal chemistry, 2002-12, Vol.45 (25), p.5415-5418

2002

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The dopamine D1 receptor agonist SKF-82958 serves as a discriminative stimulus in the rat

European journal of pharmacology, 2000-01, Vol.388 (2), p.125-131

2000

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Enhancement of pharmacokinetic properties and in vivo efficacy of benzylidene ketal M2 muscarinic receptor antagonists via benzamide modification

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3479-3482

2002

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Metabolic stabilization of benzylidene ketal M2 muscarinic receptor antagonists via halonaphthoic acid substitution

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (17), p.2311-2314

2001

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Benzylidene ketal derivatives as M2 muscarinic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (24), p.2727-2730

2000

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Central effects of adenosine analogs on locomotor activity in mice and antagonism of caffeine

Brain research, 1983-08, Vol.272 (2), p.392-395

1983

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SCH 57790, a selective muscarinic M 2 receptor antagonist, releases acetylcholine and produces cognitive enhancement in laboratory animals

European journal of pharmacology, 2001-11, Vol.431 (2), p.189-200

2001

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Behavioral and physiological effects of xanthines in nonhuman primates

Psychopharmacologia, 1997-01, Vol.129 (1), p.1-14

1997

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Cyclic urea derivatives as potent NK sub(1) selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (4), p.1065-1069

2006

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Cyclic urea derivatives as potent NK 1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Bioorganic & medicinal chemistry letters, 2006, Vol.16 (4), p.1065-1069

2006

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Cyclic urea derivatives as potent NK1 selective aantagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Bioorganic & medicinal chemistry letters, 2006, Vol.16 (4), p.1065-1069

2006

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The dopamine D 1 receptor agonist SKF-82958 serves as a discriminative stimulus in the rat

European journal of pharmacology, 2000-01, Vol.388 (2), p.125-131

2000

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Improving the Oral Efficacy of CNS Drug Candidates: Discovery of Highly Orally Efficacious Piperidinyl Piperidine M 2 Muscarinic Receptor Antagonists

Journal of medicinal chemistry, 2002-12, Vol.45 (25), p.5415-5418

2002

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Cholinergic improvement of a naturally-occurring memory deficit in the young rat

Brain research, 1996-01, Vol.707 (1), p.13-21

1996

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Cyclic urea derivatives as potent NK 1 selective antagonists

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (17), p.3896-3899

2005

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Enhancement of pharmacokinetic properties and in vivo efficacy of benzylidene ketal M 2 muscarinic receptor antagonists via benzamide modification

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3479-3482

2002

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Benzylidene ketal derivatives as M 2 muscarinic receptor antagonists

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (24), p.2727-2730

2000

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Metabolic stabilization of benzylidene ketal M 2 muscarinic receptor antagonists via halonaphthoic acid substitution

Bioorganic & medicinal chemistry letters, 2001-09, Vol.11 (17), p.2311-2314

2001

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The anxiolytic-like effects of the novel, orally active nociceptin opioid receptor agonist 8-[bis(2-methylphenyl)methyl]-3-phenyl-8-azabicyclo[3.2.1]octan-3-ol (SCH 221510)

Cyclic urea derivatives as potent NK1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Interdisciplinary Teaching of Pharmacology and Genetics: Comparing Two Different Active Learning Models in Medical School

The Gerbil Elevated Plus-maze II: Anxiolytic-like Effects of Selective Neurokinin NK1 Receptor Antagonists

The Gerbil Elevated Plus-Maze I: Behavioral Characterization and Pharmacological Validation

Cyclic urea derivatives as potent NK1 selective antagonists

SCH 57790, a selective muscarinic M2 receptor antagonist, releases acetylcholine and produces cognitive enhancement in laboratory animals

Improving the Oral Efficacy of CNS Drug Candidates: Discovery of Highly Orally Efficacious Piperidinyl Piperidine M2 Muscarinic Receptor Antagonists

The dopamine D1 receptor agonist SKF-82958 serves as a discriminative stimulus in the rat

Enhancement of pharmacokinetic properties and in vivo efficacy of benzylidene ketal M2 muscarinic receptor antagonists via benzamide modification

Metabolic stabilization of benzylidene ketal M2 muscarinic receptor antagonists via halonaphthoic acid substitution

Benzylidene ketal derivatives as M2 muscarinic receptor antagonists

Central effects of adenosine analogs on locomotor activity in mice and antagonism of caffeine

SCH 57790, a selective muscarinic M 2 receptor antagonist, releases acetylcholine and produces cognitive enhancement in laboratory animals

Behavioral and physiological effects of xanthines in nonhuman primates

Cyclic urea derivatives as potent NK sub(1) selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Cyclic urea derivatives as potent NK 1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions

Cyclic urea derivatives as potent NK1 selective aantagonists. Part II: Effects of fluoro and benzylic methyl substitutions

The dopamine D 1 receptor agonist SKF-82958 serves as a discriminative stimulus in the rat

Improving the Oral Efficacy of CNS Drug Candidates: Discovery of Highly Orally Efficacious Piperidinyl Piperidine M 2 Muscarinic Receptor Antagonists

Cholinergic improvement of a naturally-occurring memory deficit in the young rat

Cyclic urea derivatives as potent NK 1 selective antagonists

Enhancement of pharmacokinetic properties and in vivo efficacy of benzylidene ketal M 2 muscarinic receptor antagonists via benzamide modification

Benzylidene ketal derivatives as M 2 muscarinic receptor antagonists

Metabolic stabilization of benzylidene ketal M 2 muscarinic receptor antagonists via halonaphthoic acid substitution

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