Nagatomo T | Dep. Of Pharmacology Fac. Of Pharmaceutical Sciences Niigata Univ. Of Pharmacy And Applied Life Scie

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著作論文

Constitutively Active Mutant N111G of Angiotensin II Type 1 (AT_1) Receptor Induces Homologous Internalization Through Mediation of AT_1-Receptor Antagonist
Assessment of Binding Affinity to 5-Hydroxytryptamine 2A (5-HT_) Receptor and Inverse Agonist Activity of Naftidrofuryl : Comparison With Those of Sarpogrelate
Pharmacological Differences between Liu-Jun-Zi-Tang, a Traditional Chinese Herbal Medicine, and Domperidone on Isolated Guinea-Pig Ileum(Pharmacology)
Actions of Liu-Jun-Zi-Tang, a Traditional Chinese Herbal Medicine, on Exogenous and Endogenous Opioid Systems in Isolated Guinea Pig Ileum
Mutation of Important Amino Acid Residue of Asp104Lys in Human β_1-Adrenergic Receptor Triggers Functional and Constitutive Inactivation(Pharmacology)
Identification of a Key Amino Acid of the Human 5-HT_ Serotonin Receptor Important for Sarpogrelate Binding
Selectivity of Sarpogrelate to the Recombinant Human 5-HT_ Receptors as Assessed by Molecular Pharmacology and Molecular Modeling
Inverse Agonist Activity of Sarpogrelate, a Selective 5-HT_-Receptor Antagonist, at the Constitutively Active Human 5-HT_ Receptor
Assessment of Affinities and Dissociation Potencies of Several 5-HT_2 Antagonists to and from M_2 Muscarinic Receptor in Rat Heart Membranes(Pharmacology)
Molecular modeling of the interaction of sarpogrelate and human 5-HT_, 5-HT_ and 5-HT_ receptor subtypes
Chronic Myocarditis and Angiotensin-II Receptor Antagonist (TCV-116)
Changes in α_1-and β_1-Adrenergic Receptors and Calcium Ion Binding Sites in the Fetal Myocardium of Spontaneously Hypertensive Rats (SHR)
Internalization of Constitutively Active N111G Mutant of AT1 Receptor Induced by Angiotensin II–Receptor Antagonists Candesartan, Losartan, and Telmisartan: Comparison With Valsartan
Mutational Analysis of the α_-Adrenergic Receptor Binding Pocket of Antagonists by Radioligand Binding Assay(Pharmacology)
Amino Acids of the Human α_-Adrenergic Receptor Involved in Antagonist Binding
Asp125 and Thr130 in Transmembrane Domain 3 Are Major Sites of α_-Adrenergic Receptor Antagonist Binding(Pharmacology)
Differential Inhibition by Oxygen Radicals of Vasoactive Amines-Induced Contractions in the Porcine Coronary Artery(Pharmacology)
Beta-Blockers Show Inverse Agonism to a Novel Constitutively Active Mutant of β_1-Adrenoceptor
Pharmacological and Molecular Characterization of Novel SWR-Compounds for β-Adrenergic Receptors as assessed by Molecular Modeling, Site-Directed Mutagenesis, Binding Affinity and Functional Activity
Identification of Amino Acid Residues Important for Sarpogrelate Binding to the Human 5-Hydroxytryptamine_ Serotonin Receptor
Site-Directed Mutagenesis of the Serotonin 5-Hydroxytryptamine_ Receptor : Identification of Amino Acids Responsible for Sarpogrelate Binding(Pharmacology)
Effects of Sarpogrelate, a Novel 5-HT_2 Antagonist, on 5-HT-Induced Endothelium-Dependent Relaxations in Porcine Coronary Artery
Assessment of Affinity and Dissociation Ability of a Newly Synthesized 5-HT_2 Antagonist, AT-1015: Comparison With Other 5-HT_2 Antagonists
Binding Affinity of a Newly Synthesized 5-HT_2 Antagonist, AT-1015(N-[2-[4-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)-piperidino]ethyl]-1-formyl-4-piperidinecarboxamide Monohydrochloride Monohydrate), in the Rabbit Platelet Membrane
Assessment of β_2- and β_3-Adrenoceptors in Rat White Adipose Tissues by Radioligand Binding Assay
Effects of Chronic Administration of Bopindolol on the Binding Characteristics of Cardiac α_-, α_-, β_1- and β_2-Adrenoceptor Subtypes in Cardiac Muscles of Spontaneously Hypertensive Rats (SHR)
Anti-obesity and Anti-diabetic Activities of a New β_3 Adrenergic Receptor Agonist, (S)-(Z)-[4-[[1-[2-[(2-Hydroxy-3-phenoxypropyl)]amino]athyl]-1-propenyl]phenoxy] Acetic Acid Ethanedioic Acid (SWR-0342SA), in KK-A^y Mice
Molecular Characterization of Pharmacological Properties and Selectivity of SWR-0315NA for β_3-Adrenoceptors (Pharmacology)
Structure-activity relationship studies of phenoxypropanolamine derivatives for β_3-adrenergic activity
β-Adrenoceptors: Three-Dimensional Structures and Binding Sites for Ligands
Inhibitory Effects of a Newly Synthesized 5-HT_2 Receptor Antagonist, AT-1015 (N-[2-[4-(5H-Dibenzo[a, d]cyclohepten-5-ylidene)piperidino]-ethyl]-1-formyl-4-piperidinecarboxamide Monohydrochloride Monohydrate), on Contraction and Relaxation of Pig Coronary
Affinity for [^3H]Iloprost Binding Sites and cAMP Synthesis Activityof a 3-Oxa-methano Prostaglandin I_1Analog, SM-10906,in Human Platelets and Endothelial Cells
Slow Dissociation of Long-Acting Ca^ Antagonist Amlodipine from ^3H-PN200-110 Binding Sites in Membranes of Rat Hearts and Brains
cAMP-Independent Chloride Secretion Activated by a Vasoactive Intestinal Peptide in a Monolayer Culture of Human Bronchinal Epithelial Cells
Beta-blocking Potency and Selectivity of Bopindolol and Its Two Metabolites for β_1-and β_2-Adrenergic Receptors as Assessed by Radioligand Binding Assay
Binding Characteristics of [^3H] Ketanserin for Serotonin-2 Receptor in the Rabbit Platelet
Binding Characteristics of α_1-Adrenoceptors in Bovine Prostate Using a Radioligand Binding Assay
MCI-9042 : High Affinity for Serotonergic Receptors as Assessed by Radioligand Binding Assay
Three Binding Sites of ^I-Iodocyanopindolol, i.e. β_1,β_2-Adrenergic and 5HT_-Serotonergic Receptors in Rat Brain Determined by the Displacement and Scatchard Analysis
BINDING CHARACTERISTICS OF 3H-DIHYDROALPRENOLOL TO β-ADRENOCEPTORS OF RAT HEART TREATED WITH NEURAMINIDASE

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