quinidine has been researched along with hexobarbital in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (44.44) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (44.44) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Topliss, JG; Yoshida, F | 1 |
Abraham, MH; Acree, WE; Ibrahim, A | 1 |
Lombardo, F; Obach, RS; Waters, NJ | 1 |
Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV | 1 |
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
Hanano, M; Harashima, H; Iga, T; Sawada, Y; Sugiyama, Y | 1 |
Almirante, L; Murmann, W; Saccani-Guelfi, M | 1 |
Bernauer, W; Hahn, F | 1 |
van Zwieten, PA | 1 |
9 other study(ies) available for quinidine and hexobarbital
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 |
Air to lung partition coefficients for volatile organic compounds and blood to lung partition coefficients for volatile organic compounds and drugs.
Topics: Air; Animals; Humans; Lung; Organic Chemicals; Probability; Rats; Tissue Distribution; Volatilization | 2008 |
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 |
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Prediction of serum concentration time course of quinidine in human using a physiologically based pharmacokinetic model developed from the rat.
Topics: Animals; Antipyrine; Half-Life; Hexobarbital; Humans; Kidney; Kinetics; Liver; Metabolic Clearance Rate; Models, Biological; Phenytoin; Quinidine; Rats; Time Factors | 1986 |
Effects of hexobarbitone, ether, morphine, and urethane upon the acute toxicity of propranolol and D-(--)-INPEA.
Topics: Amino Alcohols; Animals; Atropine; Bradycardia; Central Nervous System; Drug Synergism; Ethers; Heart Arrest; Heart Rate; Hexobarbital; Lidocaine; Male; Mice; Morphine; Nitrobenzenes; Propranolol; Quinidine; Seizures; Sleep; Urethane | 1966 |
Studies on heart anaphylaxis. II. Effect of histamine and antigen on heart failure in heart-lung-preparation of guinea-pigs.
Topics: Anaphylaxis; Animals; Antigen-Antibody Reactions; Aorta; Blood Pressure; Calcium Chloride; Cardiac Output; Cardiovascular Diseases; Female; Guinea Pigs; Heart; Heart Rate; Heart-Lung Machine; Hexobarbital; Histamine; Histamine H1 Antagonists; Male; Norepinephrine; Ovalbumin; Pyridines; Quinidine; Reserpine; Tyramine | 1969 |
Decrease in ionic permeability of the cell membrane in guinea-pig atrial tissue by treatment with antifibrillatory agents and hexobarbitone, determined by means of 86Rb.
Topics: Animals; Anti-Arrhythmia Agents; Cell Membrane Permeability; Guinea Pigs; Heart; Heart Atria; Heart Rate; Hexobarbital; In Vitro Techniques; Muscle Contraction; Propranolol; Quinidine; Radioisotopes; Rubidium; Tetracaine | 1969 |