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Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist

British journal of pharmacology, 2009-02, Vol.143 (5), p.649-661

2009

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Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist

British journal of pharmacology, 2004-11, Vol.143 (5), p.649-661

2004

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Conformational considerations in the design of dual antagonists of platelet-activating factor (PAF) and histamine

Bioorganic & medicinal chemistry, 1999-07, Vol.7 (7), p.1413-1423

1999

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Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist

British journal of pharmacology, 2009-01, Vol.144 (1), p.145-145

2009

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Selective Blockade of the Capsaicin Receptor TRPV1 Attenuates Bone Cancer Pain

The Journal of neuroscience, 2005-03, Vol.25 (12), p.3126-3131

2005

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Identification and Biological Evaluation of 4-(3-Trifluoromethylpyridin-2-yl)piperazine-1-carboxylic Acid (5-Trifluoromethylpyridin-2-yl)amide, a High Affinity TRPV1 (VR1) Vanilloid Receptor Antagonist

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.1857-1872

2005

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Discovery of novel nonpeptide tricyclic inhibitors of ras farnesyl protein transferase

Bioorganic & medicinal chemistry, 1997-01, Vol.5 (1), p.101-113

1997

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Synthesis of C-11 Methyl-Substituted Benzocycloheptapyridine Inhibitors of Farnesyl Protein Transferase

Organic letters, 1999-11, Vol.1 (9), p.1371-1373

1999

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Palladium-Catalyzed Coupling of Pyrazole Triflates with Arylboronic Acids

Journal of organic chemistry, 2005-05, Vol.70 (10), p.4188-4190

2005

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Preparation and Biological Evaluation of Indole, Benzimidazole, and Thienopyrrole Piperazine Carboxamides: Potent Human Histamine H 4 Antagonists

Journal of medicinal chemistry, 2005-12, Vol.48 (26), p.8289-8298

2005

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A New Class of Diamine-Based Human Histamine H 3 Receptor Antagonists: 4-(Aminoalkoxy)benzylamines

Journal of medicinal chemistry, 2003-08, Vol.46 (18), p.3938-3944

2003

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Synthesis of A series of sulfinic acid analogs of GABA and evaluation of their GABAB receptor affinities

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (21), p.3059-3064

1998

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Non-imidazole heterocyclic histamine H 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2003-05, Vol.13 (10), p.1767-1770

2003

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4-Phenoxypiperidines: Potent, Conformationally Restricted, Non-Imidazole Histamine H 3 Antagonists

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.2229-2238

2005

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Novel substituted 4-phenyl-[1,3]dioxanes: potent and selective orexin receptor 2 (OX 2R) antagonists

Bioorganic & medicinal chemistry letters, 2004-08, Vol.14 (16), p.4225-4229

2004

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The TRPV1 Vanilloid Receptor: A Target for Therapeutic Intervention

Annual Reports in Medicinal Chemistry, 2005, Vol.40, p.185-198

2005

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Effects of histamine H 3 antagonists and donepezil on learning and mnemonic deficits induced by pentylenetetrazol kindling in weanling mice

Neuropharmacology, 2006-03, Vol.50 (4), p.404-411

2006

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Tomoxiprole Selectively Inhibits Cyclooxygenase-2

Prostaglandins, 1997-12, Vol.54 (6), p.891-898

1997

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Aplysamine-1 and related analogs as histamine H 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (4), p.897-900

2006

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Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist

British journal of pharmacology, 2005-01, Vol.144 (1), p.145-145

2005

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Novel human histamine H 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (22), p.3309-3312

2002

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A Short Synthesis of Albuterol

Synthesis (Stuttgart), 1988, Vol.1988 (12), p.966-968

1988

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Synthesis and structure–activity relationships of oxime neurokinin antagonists: discovery of potent arylamides

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.141-145

2002

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Reductive N-alkylation of secondary amines with [2-11C]acetone

Journal of labelled compounds & radiopharmaceuticals, 2003-10, Vol.46 (11), p.1075-1085

2003

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Synthesis of corticoids from 9α-hydroxyandrost-4-ene-3,17-dione

Journal of organic chemistry, 1992-01, Vol.57 (3), p.961-965

1992

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Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist

Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist

Conformational considerations in the design of dual antagonists of platelet-activating factor (PAF) and histamine

Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist

Selective Blockade of the Capsaicin Receptor TRPV1 Attenuates Bone Cancer Pain

Identification and Biological Evaluation of 4-(3-Trifluoromethylpyridin-2-yl)piperazine-1-carboxylic Acid (5-Trifluoromethylpyridin-2-yl)amide, a High Affinity TRPV1 (VR1) Vanilloid Receptor Antagonist

Discovery of novel nonpeptide tricyclic inhibitors of ras farnesyl protein transferase

Synthesis of C-11 Methyl-Substituted Benzocycloheptapyridine Inhibitors of Farnesyl Protein Transferase

Palladium-Catalyzed Coupling of Pyrazole Triflates with Arylboronic Acids

Preparation and Biological Evaluation of Indole, Benzimidazole, and Thienopyrrole Piperazine Carboxamides: Potent Human Histamine H 4 Antagonists

A New Class of Diamine-Based Human Histamine H 3 Receptor Antagonists: 4-(Aminoalkoxy)benzylamines

Synthesis of A series of sulfinic acid analogs of GABA and evaluation of their GABAB receptor affinities

Non-imidazole heterocyclic histamine H 3 receptor antagonists

4-Phenoxypiperidines: Potent, Conformationally Restricted, Non-Imidazole Histamine H 3 Antagonists

Novel substituted 4-phenyl-[1,3]dioxanes: potent and selective orexin receptor 2 (OX 2R) antagonists

The TRPV1 Vanilloid Receptor: A Target for Therapeutic Intervention

Effects of histamine H 3 antagonists and donepezil on learning and mnemonic deficits induced by pentylenetetrazol kindling in weanling mice

Tomoxiprole Selectively Inhibits Cyclooxygenase-2

Aplysamine-1 and related analogs as histamine H 3 receptor antagonists

Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist

Novel human histamine H 3 receptor antagonists

A Short Synthesis of Albuterol

Synthesis and structure–activity relationships of oxime neurokinin antagonists: discovery of potent arylamides

Reductive N-alkylation of secondary amines with [2-11C]acetone

Synthesis of corticoids from 9α-hydroxyandrost-4-ene-3,17-dione

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