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BF2.649 [1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, hydrochloride], a nonimidazole inverse agonist/antagonist at the human histamine H3 receptor: Preclinical pharmacology

The Journal of pharmacology and experimental therapeutics, 2007-01, Vol.320 (1), p.365

2007

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Discovery of nanomolar ligands with novel scaffolds for the histamine H4 receptor by virtual screening

European journal of medicinal chemistry, 2017-01, Vol.125, p.565-572

2017

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Improving selectivity of dopamine D3 receptor ligands

Bioorganic & medicinal chemistry letters, 2016-02, Vol.26 (3), p.885-888

2016

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Structure of the human glycogen-associated protein phosphatase 1 regulatory subunit hGM: Homology modeling revealed an (α/β)8-barrel-like fold in the multidomain protein

Protein science, 1999-12, Vol.8 (12), p.2570-2579

1999

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Inhibition of the cardiac electrogenic sodium bicarbonate cotransporter reduces ischemic injury

Cardiovascular research, 2001-12, Vol.52 (3), p.387-396

2001

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Matrix metalloproteinase expression in cardiac myocytes following myocardial infarction in the rabbit

Life sciences (1973), 2001-01, Vol.68 (7), p.799-814

2001

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EDG1 Receptor Stimulation Leads to Cardiac Hypertrophy in Rat Neonatal Myocytes

Journal of molecular and cellular cardiology, 2001-09, Vol.33 (9), p.1589-1606

2001

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BF2.649 [1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, Hydrochloride], a Nonimidazole Inverse Agonist/Antagonist at the Human Histamine H 3 Receptor: Preclinical Pharmacology

The Journal of pharmacology and experimental therapeutics, 2007-01, Vol.320 (1), p.365-375

2007

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COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes

Journal of molecular biology, 1999-11, Vol.294 (2), p.443-456

1999

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Turnover rates of the canine cardiac Na,K-ATPases

FEBS letters, 1993-09, Vol.330 (3), p.297-301

1993

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Specific Modulation of two Neuronal Digitalis Receptors by Anaesthesia

Journal of receptors and signal transduction, 1997-01, Vol.17 (1-3), p.137-147

1997

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Biophysical interaction between phospholamban and protein phosphatase 1 regulatory subunit GM

FEBS letters, 1998-11, Vol.439 (3), p.224-230

1998

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cDNA Sequence and Characterization of the Gene that Encodes Human Myotrophin/V-1 Protein, a Mediator of Cardiac Hypertrophy

Journal of molecular and cellular cardiology, 1999-04, Vol.31 (4), p.705-719

1999

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Cordil Reversibly Inhibits the Na, K-ATPase from Outside of the Cell Membrane. Role of K-dependent Dephosphorylation

Journal of receptor research, 1993, Vol.13 (7), p.1083-1092

1993

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Comparative properties of alpha and alpha plus subunits in adult rat brain and heart

Progress in clinical and biological research, 1988, Vol.268B, p.43

1988

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Mechanism underlying the strong positive inotropic effects of LND-623 : Specific inhibition of Na, K-ATPase isoforms and exclusion of cellular sites of contractile control

Cardiovascular drugs and therapy, 1998-12, Vol.12 (6), p.585-594

1998

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Relationship Between Biochemical and Functional Effects of Protein Phosphatase 1 Inhibitors in Rabbit Cardiac Skinned Fibers

Journal of molecular and cellular cardiology, 1998-10, Vol.30 (10), p.1945-1954

1998

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Neuropeptide AF and FF Modulation of Adipocyte Metabolism. Primary Insights from Functional Genomics and Effects on [beta]-Adrenergic Responsiveness

The Journal of biological chemistry, 2002-10, Vol.277 (42), p.39169-39178

2002

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Immunodetection and enzymatic characterization of the α3-isoform of Na,K-ATPase in dog heart

FEBS letters, 1994-07, Vol.348 (1), p.55-60

1994

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Efficacy and safety of the novel Na+,K(+)-ATPase inhibitor 20R 14 beta-amino 3 beta-rhamnosyl 5 beta-pregnan 20 beta-ol in a dog model of heart failure

Arzneimittel-Forschung, 1992-11, Vol.42 (11), p.1301

1992

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Immunodetection and enzymatic characterization of the alpha 3-isoform of Na,K-ATPase in dog heart

FEBS letters, 1994-07, Vol.348 (1), p.55-60

1994

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An organophosphorus compound, Vx, selectively inhibits the rat cardiac Na +,K +-ATPase α 1 isoform Biochemical basis of the cardiotoxicity of Vx

FEBS letters, 1991-04, Vol.281 (1), p.145-148

1991

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Inhibition of cardiac (Na +, K +)-ATPase isozymes by LND 623

Biochemical pharmacology, 1991-12, Vol.42, p.S223-S224

1991

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Diminished toxicity of ouabain in the hypertrophied rat heart

Pflügers Archiv, 1989-07, Vol.414 (3), p.311-316

1989

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Immunodetection and functional expression of alpha 3 isoform of Na,K-ATPase in dog heart

Journal of molecular and cellular cardiology, 1992-11, Vol.24, p.26-26

1992

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BF2.649 [1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, hydrochloride], a nonimidazole inverse agonist/antagonist at the human histamine H3 receptor: Preclinical pharmacology

Discovery of nanomolar ligands with novel scaffolds for the histamine H4 receptor by virtual screening

Improving selectivity of dopamine D3 receptor ligands

Structure of the human glycogen-associated protein phosphatase 1 regulatory subunit hGM: Homology modeling revealed an (α/β)8-barrel-like fold in the multidomain protein

Inhibition of the cardiac electrogenic sodium bicarbonate cotransporter reduces ischemic injury

Matrix metalloproteinase expression in cardiac myocytes following myocardial infarction in the rabbit

EDG1 Receptor Stimulation Leads to Cardiac Hypertrophy in Rat Neonatal Myocytes

BF2.649 [1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, Hydrochloride], a Nonimidazole Inverse Agonist/Antagonist at the Human Histamine H 3 Receptor: Preclinical Pharmacology

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes

Turnover rates of the canine cardiac Na,K-ATPases

Specific Modulation of two Neuronal Digitalis Receptors by Anaesthesia

Biophysical interaction between phospholamban and protein phosphatase 1 regulatory subunit GM

cDNA Sequence and Characterization of the Gene that Encodes Human Myotrophin/V-1 Protein, a Mediator of Cardiac Hypertrophy

Cordil Reversibly Inhibits the Na, K-ATPase from Outside of the Cell Membrane. Role of K-dependent Dephosphorylation

Comparative properties of alpha and alpha plus subunits in adult rat brain and heart

Mechanism underlying the strong positive inotropic effects of LND-623 : Specific inhibition of Na, K-ATPase isoforms and exclusion of cellular sites of contractile control

Relationship Between Biochemical and Functional Effects of Protein Phosphatase 1 Inhibitors in Rabbit Cardiac Skinned Fibers

Neuropeptide AF and FF Modulation of Adipocyte Metabolism. Primary Insights from Functional Genomics and Effects on [beta]-Adrenergic Responsiveness

Immunodetection and enzymatic characterization of the α3-isoform of Na,K-ATPase in dog heart

Efficacy and safety of the novel Na+,K(+)-ATPase inhibitor 20R 14 beta-amino 3 beta-rhamnosyl 5 beta-pregnan 20 beta-ol in a dog model of heart failure

Immunodetection and enzymatic characterization of the alpha 3-isoform of Na,K-ATPase in dog heart

An organophosphorus compound, Vx, selectively inhibits the rat cardiac Na +,K +-ATPase α 1 isoform Biochemical basis of the cardiotoxicity of Vx

Inhibition of cardiac (Na +, K +)-ATPase isozymes by LND 623

Diminished toxicity of ouabain in the hypertrophied rat heart

Immunodetection and functional expression of alpha 3 isoform of Na,K-ATPase in dog heart

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