propranolol has been researched along with prilocaine in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (22.22) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (55.56) | 29.6817 |
2010's | 2 (22.22) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Carrupt, PA; Guillarme, D; Henchoz, Y; Rudaz, S; Veuthey, JL | 1 |
Lombardo, F; Obach, RS; Waters, NJ | 1 |
Bard, B; Carrupt, PA; Martel, S | 1 |
Chen, L; He, Z; Li, H; Liu, J; Liu, X; Sui, X; Sun, J; Wang, Y; Zhang, W | 1 |
Brouillette, WJ; Brown, GB; Zha, C | 1 |
Porzig, H | 1 |
Satoh, H | 1 |
Deryabina, MA; Hansen, SH; Jensen, H | 1 |
Danède, F; Delplace, C; Descamps, M; Klose, D; Kreye, F; Siepmann, F; Siepmann, J | 1 |
9 other study(ies) available for propranolol and prilocaine
Article | Year |
---|---|
High-throughput log P determination by ultraperformance liquid chromatography: a convenient tool for medicinal chemists.
Topics: Chemical Phenomena; Chemistry, Pharmaceutical; Chemistry, Physical; Chromatography, Liquid; Mathematics; Pharmaceutical Preparations; Software | 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 |
Lipophilicity of basic drugs measured by hydrophilic interaction chromatography.
Topics: Chemistry, Pharmaceutical; Chromatography; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Pharmaceutical Preparations; Solubility; Technology, Pharmaceutical | 2009 |
Prediction of volume of distribution values in human using immobilized artificial membrane partitioning coefficients, the fraction of compound ionized and plasma protein binding data.
Topics: Blood Proteins; Chemistry, Physical; Computer Simulation; Humans; Membranes, Artificial; Models, Biological; Pharmaceutical Preparations; Protein Binding; Tissue Distribution | 2009 |
A highly predictive 3D-QSAR model for binding to the voltage-gated sodium channel: design of potent new ligands.
Topics: Ligands; Models, Molecular; Quantitative Structure-Activity Relationship; Voltage-Gated Sodium Channels | 2014 |
Comparative study of the effects of propranolol and tetracaine on cation movements in resealed human red cell ghosts.
Topics: Adenosine Triphosphate; Biological Transport, Active; Calcium; Cell Membrane Permeability; Erythrocytes; Humans; In Vitro Techniques; Intracellular Fluid; Lidocaine; Potassium; Practolol; Prilocaine; Propranolol; Sodium; Tetracaine; Tetraethylammonium Compounds | 1975 |
Comparison of the chronotropic responses to local anesthetics (procaine, lidocaine, prilocaine, mepivacaine and bupivacaine) of the canine sinus node in situ.
Topics: Anesthetics, Local; Animals; Bupivacaine; Dogs; Dose-Response Relationship, Drug; Female; Heart Rate; Lidocaine; Male; Mepivacaine; Prilocaine; Procaine; Propranolol; Reserpine; Sinoatrial Node; Tetrodotoxin | 1981 |
Molecular interactions in lipophilic environments studied by electrochemistry at interfaces between immiscible electrolyte solutions.
Topics: Buffers; Cholesterol; Diflunisal; Electrochemistry; Electrolytes; Hydrophobic and Hydrophilic Interactions; Lidocaine; Ligands; Prilocaine; Propranolol; Solutions; Warfarin | 2008 |
Impact of the experimental conditions on drug release from parenteral depot systems: From negligible to significant.
Topics: Dexamethasone; Drug Implants; Ibuprofen; Infusions, Parenteral; Kinetics; Lactic Acid; Lidocaine; Lipids; Particle Size; Polyglycolic Acid; Polylactic Acid-Polyglycolic Acid Copolymer; Prilocaine; Propranolol; Theophylline; X-Ray Diffraction | 2012 |