Page last updated: 2024-08-16

pyrilamine and u 73122

pyrilamine has been researched along with u 73122 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gibson, WJ; Hughes, SA; Young, JM1
Chang, HT; Chen, WC; Chou, KJ; Huang, JK; Jan, CR; Law, YP; Lee, KC; Lo, YK; Su, W; Tang, KY; Wang, JL1
Basta-Kaim, A; Budziszewska, B; Jaworska-Feil, L; Kubera, M; Lasoń, W; Leśkiewicz, M; Tetich, M1
Baldo, CF; Capellini, VK; Celotto, AC; Evora, PR; Rodrigues, AJ; Viaro, F; Vicente, WV1
Liang, H; Liu, B; Liu, L; Zhang, H1

Other Studies

5 other study(ies) available for pyrilamine and u 73122

ArticleYear
The interaction of U-73122 with the histamine H1 receptor: implications for the use of U-73122 in defining H1 receptor-coupled signalling pathways.
    Naunyn-Schmiedeberg's archives of pharmacology, 2000, Volume: 362, Issue:6

    Topics: Animals; Binding, Competitive; Estrenes; Ethylmaleimide; Guinea Pigs; Inhibitory Concentration 50; Kinetics; Male; Phosphodiesterase Inhibitors; Pyrilamine; Pyrrolidinones; Receptors, Histamine H1; Tritium; Type C Phospholipases

2000
Mechanism underlying histamine-induced intracellular Ca2+ movement in PC3 human prostate cancer cells.
    Pharmacological research, 2001, Volume: 44, Issue:6

    Topics: Calcium; Calcium-Transporting ATPases; Endoplasmic Reticulum; Enzyme Inhibitors; Estrenes; Fluorescent Dyes; Fura-2; Histamine; Histamine H1 Antagonists; Histamine H2 Antagonists; Humans; Inositol 1,4,5-Trisphosphate; Ion Transport; Male; Phosphodiesterase Inhibitors; Prostatic Neoplasms; Pyrilamine; Pyrrolidinones; Thapsigargin; Tumor Cells, Cultured; Type C Phospholipases

2001
Chlorpromazine inhibits the glucocorticoid receptor-mediated gene transcription in a calcium-dependent manner.
    Neuropharmacology, 2002, Volume: 43, Issue:6

    Topics: Animals; Antipsychotic Agents; Calcimycin; Calcium; Calcium Channel Blockers; Cell Line; Cell Line, Transformed; Chloramphenicol O-Acetyltransferase; Chlorpromazine; Clozapine; Colforsin; Cyclic AMP; Dose-Response Relationship, Drug; Drug Synergism; Enzyme Inhibitors; Estrenes; Fibroblasts; Gene Expression Regulation; Genes, Reporter; Haloperidol; Histamine; Histamine H1 Antagonists; Ionophores; Mammary Tumor Virus, Mouse; Mice; Nifedipine; Phorbol Esters; Phosphodiesterase Inhibitors; Protein Kinase C; Protein Kinase C-alpha; Pyrilamine; Pyrrolidinones; Raclopride; Receptors, Glucocorticoid; Remoxipride; Sulfonamides; Sulpiride; Tetradecanoylphorbol Acetate; Thionucleotides; Transcription, Genetic; Type C Phospholipases

2002
Compound 48/80 induces endothelium-dependent and histamine release-independent relaxation in rabbit aorta.
    Nitric oxide : biology and chemistry, 2008, Volume: 18, Issue:2

    Topics: Animals; Aorta; Cimetidine; Endothelium, Vascular; Estrenes; Histamine H1 Antagonists; Histamine Release; In Vitro Techniques; Male; Muscle Relaxation; NG-Nitroarginine Methyl Ester; Nitric Oxide; p-Methoxy-N-methylphenethylamine; Pyrilamine; Pyrrolidinones; Rabbits

2008
Phosphatidylinositol 4,5-bisphosphate hydrolysis mediates histamine-induced KCNQ/M current inhibition.
    American journal of physiology. Cell physiology, 2008, Volume: 295, Issue:1

    Topics: Animals; Calcium; Cell Line; Cell Membrane; Estrenes; Histamine; Humans; Hydrolysis; Ion Channel Gating; KCNQ2 Potassium Channel; KCNQ3 Potassium Channel; Neurons; Phosphatidylinositol 4,5-Diphosphate; Pyrilamine; Pyrrolidinones; Rats; Receptors, Histamine H1; Type C Phospholipases

2008