glyburide has been researched along with cifenline in 14 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 7 (50.00) | 18.2507 |
2000's | 5 (35.71) | 29.6817 |
2010's | 2 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Topliss, JG; Yoshida, F | 1 |
Lombardo, F; Obach, RS; Waters, NJ | 1 |
Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV | 1 |
Chang, G; El-Kattan, A; Miller, HR; Obach, RS; Rotter, C; Steyn, SJ; Troutman, MD; Varma, MV | 1 |
Afshari, CA; Chen, Y; Dunn, RT; Hamadeh, HK; Kalanzi, J; Kalyanaraman, N; Morgan, RE; van Staden, CJ | 1 |
Arita, M; Kiyosue, T; Sato, T; Wu, B | 1 |
Okamoto, K; Sakuta, H; Watanabe, Y | 1 |
Arita, M; Kiyosue, T; Nakamura, S; Sato, T; Wu, B | 1 |
Ai, T; Horie, M; Ishida, H; Ishida-Takahashi, A; Sasayama, S; Tsuura, Y | 1 |
Fujimoto, S; Horie, M; Ishida, H; Ishida-Takahashi, A; Kato, S; Mukai, E; Seino, Y; Tsuda, K; Tsuura, Y | 1 |
Arita, M; Sato, T; Shigematsu, S | 1 |
Horie, M; Ishida, H; Mukai, E; Noma, A; Seino, Y; Takano, M | 1 |
Horie, M; Ishida, H; Ishida-Takahashi, A; Sasayama, S; Seino, Y; Tsuji, K; Watanuki, M; Yuzuki, Y | 1 |
Brading, AF; Ito, Y; Masaki, I; Sueishi, K; Takano, M; Teramoto, N; Yonemitsu, Y; Yunoki, T | 1 |
14 other study(ies) available for glyburide and cifenline
Article | Year |
---|---|
QSAR model for drug human oral bioavailability.
Topics: Administration, Oral; Biological Availability; Humans; Models, Biological; Models, Molecular; Pharmaceutical Preparations; Pharmacokinetics; Structure-Activity Relationship | 2000 |
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding | 2008 |
Physicochemical determinants of human renal clearance.
Topics: Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kidney; Metabolic Clearance Rate; Molecular Weight | 2009 |
Physicochemical space for optimum oral bioavailability: contribution of human intestinal absorption and first-pass elimination.
Topics: Administration, Oral; Biological Availability; Humans; Intestinal Absorption; Pharmaceutical Preparations | 2010 |
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
Topics: Animals; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Biological Transport; Chemical and Drug Induced Liver Injury; Cluster Analysis; Drug-Related Side Effects and Adverse Reactions; Humans; Liver; Male; Multidrug Resistance-Associated Proteins; Pharmacokinetics; Rats; Rats, Sprague-Dawley; Recombinant Proteins; Risk Assessment; Risk Factors; Toxicity Tests | 2013 |
Blockade of 2,4-dinitrophenol induced ATP sensitive potassium current in guinea pig ventricular myocytes by class I antiarrhythmic drugs.
Topics: 2,4-Dinitrophenol; Action Potentials; Adenosine Triphosphate; Animals; Anti-Arrhythmia Agents; Dinitrophenols; Disopyramide; Flecainide; Glyburide; Guinea Pigs; Heart Ventricles; Imidazoles; Lidocaine; Mexiletine; Myocardium; Piperidines; Potassium; Procainamide; Pyridines | 1992 |
Antiarrhythmic drugs, clofilium and cibenzoline are potent inhibitors of glibenclamide-sensitive K+ currents in Xenopus oocytes.
Topics: Animals; Anti-Arrhythmia Agents; Antihypertensive Agents; Benzopyrans; Electrophysiology; Female; Glyburide; Imidazoles; Membrane Potentials; Oocytes; Potassium Channels; Pyridines; Quaternary Ammonium Compounds; Xenopus laevis | 1993 |
Cibenzoline inhibits diazoxide- and 2,4-dinitrophenol-activated ATP-sensitive K+ channels in guinea-pig ventricular cells.
Topics: 2,4-Dinitrophenol; Action Potentials; Adenosine Triphosphate; Animals; Anti-Arrhythmia Agents; Diazoxide; Dinitrophenols; Glyburide; Guinea Pigs; Heart; Heart Ventricles; Imidazoles; In Vitro Techniques; Membrane Potentials; Potassium Channels | 1993 |
Block of pancreatic ATP-sensitive K+ channels and insulinotrophic action by the antiarrhythmic agent, cibenzoline.
Topics: Animals; Anti-Arrhythmia Agents; Glyburide; Hydrogen-Ion Concentration; Hypoglycemia; Hypoglycemic Agents; Imidazoles; Insulin; Insulin Secretion; Islets of Langerhans; Male; Potassium Channels; Rats; Rats, Wistar | 1996 |
Metabolic inhibition impairs ATP-sensitive K+ channel block by sulfonylurea in pancreatic beta-cells.
Topics: 2,4-Dinitrophenol; Adenosine Triphosphate; Animals; Anti-Arrhythmia Agents; ATP-Binding Cassette Transporters; Cells, Cultured; Glyburide; Imidazoles; Islets of Langerhans; Male; Membrane Potentials; Patch-Clamp Techniques; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Inwardly Rectifying; Rats; Rats, Wistar; Receptors, Drug; Sulfonylurea Receptors | 1998 |
Class I antiarrhythmic drugs alter the severity of myocardial stunning by modulating ATP-sensitive K+ channels in guinea pig ventricular muscles.
Topics: Animals; Anti-Arrhythmia Agents; Glyburide; Guinea Pigs; Heart; Heart Ventricles; Imidazoles; Lidocaine; Male; Mexiletine; Myocardial Stunning; Potassium Channels | 1998 |
The antiarrhythmic agent cibenzoline inhibits KATP channels by binding to Kir6.2.
Topics: Adenosine Triphosphate; Animals; Anti-Arrhythmia Agents; ATP-Binding Cassette Transporters; Cloning, Molecular; COS Cells; Glyburide; Imidazoles; Patch-Clamp Techniques; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Inwardly Rectifying; Receptor Cross-Talk; Receptors, Drug; Recombinant Proteins; Sequence Deletion; Sulfonylurea Receptors; Transfection | 1998 |
Blockade of cardiac ATP-sensitive K+ channel by cibenzoline targets its pore-forming subunit.
Topics: Action Potentials; Animals; Anti-Arrhythmia Agents; Antihypertensive Agents; Cell Membrane Permeability; Cells, Cultured; Drug Interactions; Electrophysiology; Female; Glyburide; Guinea Pigs; Heart Ventricles; Hydrogen-Ion Concentration; Hypoglycemic Agents; Imidazoles; Male; Patch-Clamp Techniques; Pinacidil; Potassium Channels | 2000 |
Dual action of ZD6169, a novel K(+) channel opener, on ATP-sensitive K(+) channels in pig urethral myocytes.
Topics: Adenosine Triphosphate; Amides; Animals; Anti-Arrhythmia Agents; Benzophenones; Cells, Cultured; COS Cells; Cromakalim; Electric Conductivity; Female; Glyburide; Hypoglycemic Agents; Imidazoles; Ion Channel Gating; Membrane Potentials; Muscle, Smooth; Patch-Clamp Techniques; Potassium Channels; Potassium Channels, Inwardly Rectifying; Swine; Time Factors; Urethra; Vasodilator Agents | 2001 |