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Detection of multiple H 3 receptor affinity states utilizing [ 3 H]A‐349821, a novel, selective, non‐imidazole histamine H 3 receptor inverse agonist radioligand

British journal of pharmacology, 2009-01, Vol.148 (5), p.657-670

2009

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In vitro Optimization of Structure Activity Relationships of Analogues of A‐331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H3 Receptor Antagonists

Basic & clinical pharmacology & toxicology, 2004-09, Vol.95 (3), p.144-152

2004

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Detection of multiple H3 receptor affinity states utilizing [3H]A‐349821, a novel, selective, non‐imidazole histamine H3 receptor inverse agonist radioligand

British journal of pharmacology, 2006-07, Vol.148 (5), p.657-670

2006

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D-Amino Acid Homopiperazine Amides: Discovery of A-320436, a Potent and Selective Non-Imidazole Histamine H3-Receptor Antagonist

Archiv der Pharmazie (Weinheim), 2004-04, Vol.337 (4), p.219-229

2004

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α1 Adrenoceptor subtypes: A synopsis of their pharmacology and molecular biology

Drug development research, 1996-09, Vol.39 (1), p.54-107

Hancock, Arthur A.

1996

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Brain Localization and c‐Fos Activation of Histamine H3 Receptor Antagonists

The FASEB journal, 2006-03, Vol.20 (4), p.A245-A245

2006

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Isoform dependent differences in histamine H3 receptor constitutive activity revealed by human H3(445) and H3(365) receptors

The FASEB journal, 2007, Vol.21 (6), p.A790-A790

2007

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Effects of repeated H 3 receptor antagonist administration on H 3 receptor expression and function in rats

The FASEB journal, 2007-01, Vol.21 (6)

2007

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Effects of repeated H3 receptor antagonist administration on H3 receptor expression and function in rats

The FASEB journal, 2007, Vol.21 (6), p.A790-A790

2007

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In vitro Optimization of Structure Activity Relationships of Analogues of A‐331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H 3 Receptor Antagonists

Basic & clinical pharmacology & toxicology, 2004-09, Vol.95 (3), p.144-152

2004

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1 Adrenoceptor subtypes: A synopsis of their pharmacology and molecular biology

Drug development research, 1996-09, Vol.39 (1), p.54-107

Hancock, Arthur A.

1996

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D‐Amino Acid Homopiperazine Amides: Discovery of A‐320436, a Potent and Selective Non‐Imidazole Histamine H 3 ‐Receptor Antagonist

Archiv der Pharmazie (Weinheim), 2004-04, Vol.337 (4), p.219-229

2004

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In vitro Optimization of Structure Activity Relationships of Analogues of A-331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H sub(3) Receptor Antagonists

Basic & clinical pharmacology & toxicology, 2004-09, Vol.95 (3), p.144-152

2004

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α-Adrenoceptor assays

Current Protocols in Pharmacology, 2001-05, Vol.Chapter 4 (1), p.Unit4.5-Unit4.5

Hancock, A A

2001

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D-amino acid homopiperazine amides: discovery of A-320436, a potent and selective non-imidazole histamine H(3)-receptor antagonist

Archiv der Pharmazie (Weinheim), 2004-04, Vol.337 (4), p.219

2004

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Pharmacological antagonism of α-adrenergic agonist induced increases in canine intraurethral pressure in vivo

Drug development research, 1995-03, Vol.34 (3), p.267-275

1995

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Pharmacological characterization of A-131701, a novel ?1-adrenoceptor antagonist selective for ?1A- and ?1D-compared to ?1B-adrenoceptors

Drug development research, 1998-08, Vol.44 (4), p.140-162

1998

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A-80426, a potent and selective α2-adrenoceptor antagonist with serotonin uptake-blocking activity and putative antidepressant-like effects: II. Pharmacology profile

Drug development research, 1995-08, Vol.35 (4), p.246-260

1995

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Pharmacological characterization of A-131701, a novel α1-adrenoceptor antagonist selective for α1A- and α1D-compared to α1B-adrenoceptors

Drug development research, 1998-08, Vol.44 (4), p.140-162

1998

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A‐80426, a potent α 2 ‐adrenoceptor antagonist with serotonin uptake blocking activity and putative antidepressant‐like effects: I. Biochemical profile

Drug development research, 1995-08, Vol.35 (4), p.237-245

1995

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A‐80426, a potent and selective α 2 ‐adrenoceptor antagonist with serotonin uptake‐blocking activity and putative antidepressant‐like effects: II. Pharmacology profile

Drug development research, 1995-08, Vol.35 (4), p.246-260

1995

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A-75169 HCI: Pharmacological profile and ocular pharmacology studies of a new α-2 antagonist

Drug development research, 1993-01, Vol.28 (1), p.56-64

1993

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A-80426, a potent α2-adrenoceptor antagonist with serotonin uptake blocking activity and putative antidepressant-like effects: I. Biochemical profile

Drug development research, 1995-08, Vol.35 (4), p.237-245

1995

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A New Class of Histamine H 3 ‐Receptor Antagonists: Synthesis and Structure—Activity Relationships of 7,8,9,10‐Tetrahydro‐6H‐cyclohepta[b]quinolines

ChemInform, 2003-10, Vol.34 (42)

2003

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A New Class of Histamine H3-Receptor Antagonists: Synthesis and Structure-Activity Relationships of 7,8,9,10-Tetrahydro-6H-cyclohepta[b]quinolines

ChemInform, 2003-10, Vol.34 (42), p.no-no

2003

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Detection of multiple H 3 receptor affinity states utilizing [ 3 H]A‐349821, a novel, selective, non‐imidazole histamine H 3 receptor inverse agonist radioligand

In vitro Optimization of Structure Activity Relationships of Analogues of A‐331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H3 Receptor Antagonists

Detection of multiple H3 receptor affinity states utilizing [3H]A‐349821, a novel, selective, non‐imidazole histamine H3 receptor inverse agonist radioligand

D-Amino Acid Homopiperazine Amides: Discovery of A-320436, a Potent and Selective Non-Imidazole Histamine H3-Receptor Antagonist

α1 Adrenoceptor subtypes: A synopsis of their pharmacology and molecular biology

Brain Localization and c‐Fos Activation of Histamine H3 Receptor Antagonists

Isoform dependent differences in histamine H3 receptor constitutive activity revealed by human H3(445) and H3(365) receptors

Effects of repeated H 3 receptor antagonist administration on H 3 receptor expression and function in rats

Effects of repeated H3 receptor antagonist administration on H3 receptor expression and function in rats

In vitro Optimization of Structure Activity Relationships of Analogues of A‐331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H 3 Receptor Antagonists

1 Adrenoceptor subtypes: A synopsis of their pharmacology and molecular biology

D‐Amino Acid Homopiperazine Amides: Discovery of A‐320436, a Potent and Selective Non‐Imidazole Histamine H 3 ‐Receptor Antagonist

In vitro Optimization of Structure Activity Relationships of Analogues of A-331440 Combining Radioligand Receptor Binding Assays and Micronucleus Assays of Potential Antiobesity Histamine H sub(3) Receptor Antagonists

α-Adrenoceptor assays

D-amino acid homopiperazine amides: discovery of A-320436, a potent and selective non-imidazole histamine H(3)-receptor antagonist

Pharmacological antagonism of α-adrenergic agonist induced increases in canine intraurethral pressure in vivo

Pharmacological characterization of A-131701, a novel ?1-adrenoceptor antagonist selective for ?1A- and ?1D-compared to ?1B-adrenoceptors

A-80426, a potent and selective α2-adrenoceptor antagonist with serotonin uptake-blocking activity and putative antidepressant-like effects: II. Pharmacology profile

Pharmacological characterization of A-131701, a novel α1-adrenoceptor antagonist selective for α1A- and α1D-compared to α1B-adrenoceptors

A‐80426, a potent α 2 ‐adrenoceptor antagonist with serotonin uptake blocking activity and putative antidepressant‐like effects: I. Biochemical profile

A‐80426, a potent and selective α 2 ‐adrenoceptor antagonist with serotonin uptake‐blocking activity and putative antidepressant‐like effects: II. Pharmacology profile

A-75169 HCI: Pharmacological profile and ocular pharmacology studies of a new α-2 antagonist

A-80426, a potent α2-adrenoceptor antagonist with serotonin uptake blocking activity and putative antidepressant-like effects: I. Biochemical profile

A New Class of Histamine H 3 ‐Receptor Antagonists: Synthesis and Structure—Activity Relationships of 7,8,9,10‐Tetrahydro‐6H‐cyclohepta[b]quinolines

A New Class of Histamine H3-Receptor Antagonists: Synthesis and Structure-Activity Relationships of 7,8,9,10-Tetrahydro-6H-cyclohepta[b]quinolines

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