nitrendipine has been researched along with cocaine in 16 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (25.00) | 18.7374 |
1990's | 4 (25.00) | 18.2507 |
2000's | 5 (31.25) | 29.6817 |
2010's | 3 (18.75) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Sen, S; Sinha, N | 1 |
Creveling, CR; Daly, JW; Lewandowski, GA; McNeal, ET | 1 |
Keserü, GM | 1 |
Nagashima, R; Nishikawa, T; Tobita, M | 1 |
Lombardo, F; Obach, RS; Waters, NJ | 1 |
Jia, L; Sun, H | 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 |
Brouillette, WJ; Brown, GB; Zha, C | 1 |
Hou, X; Trouvé, R; Vicaut, E | 1 |
Manger, WM; Nahas, GG; Trouve, R | 1 |
Rubin, E; Stewart, G; Thomas, AP | 1 |
Eselin, JA; Melchert, RB; O'Dell, JF; Welder, AA | 1 |
Maillet, M; Nahas, G; Trouve, R | 1 |
Demus, JR; Nahas, G; Trouvé, R; von Sitbon, M | 1 |
Nahas, G; Trouve, R | 1 |
16 other study(ies) available for nitrendipine and cocaine
Article | Year |
---|---|
Predicting hERG activities of compounds from their 3D structures: development and evaluation of a global descriptors based QSAR model.
Topics: Computer Simulation; Ether-A-Go-Go Potassium Channels; Humans; Molecular Structure; Organic Chemicals; Quantitative Structure-Activity Relationship | 2011 |
[3H]Batrachotoxinin A 20 alpha-benzoate binding to voltage-sensitive sodium channels: a rapid and quantitative assay for local anesthetic activity in a variety of drugs.
Topics: Adrenergic alpha-Antagonists; Adrenergic beta-Antagonists; Anesthetics, Local; Animals; Batrachotoxins; Calcium Channel Blockers; Cyclic AMP; Guinea Pigs; Histamine H1 Antagonists; In Vitro Techniques; Ion Channels; Neurotoxins; Sodium; Tranquilizing Agents; Tritium | 1985 |
Prediction of hERG potassium channel affinity by traditional and hologram qSAR methods.
Topics: Cation Transport Proteins; Databases, Factual; Discriminant Analysis; Ether-A-Go-Go Potassium Channels; Holography; Linear Models; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Voltage-Gated; Quantitative Structure-Activity Relationship | 2003 |
A discriminant model constructed by the support vector machine method for HERG potassium channel inhibitors.
Topics: Animals; CHO Cells; Cricetinae; Discriminant Analysis; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Humans; Potassium Channel Blockers; Potassium Channels, Voltage-Gated | 2005 |
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 |
Support vector machines classification of hERG liabilities based on atom types.
Topics: Animals; Arrhythmias, Cardiac; CHO Cells; Computer Simulation; Cricetinae; Cricetulus; Discriminant Analysis; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Humans; Models, Chemical; Patch-Clamp Techniques; Potassium Channel Blockers; Potassium Channels, Voltage-Gated; Predictive Value of Tests; ROC Curve | 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 |
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 |
Microvascular effects of cocaine; interaction with nitrendipine and enalaprilat.
Topics: Animals; Blood Pressure; Cocaine; Drug Interactions; Enalaprilat; Injections, Intra-Arterial; Male; Microcirculation; Muscle, Smooth, Vascular; Nitrendipine; Rats; Rats, Inbred Strains; Vasoconstriction | 1991 |
Catecholamines, cocaine toxicity, and their antidotes in the rat.
Topics: Analysis of Variance; Animals; Catecholamines; Cocaine; Dopamine; Enalaprilat; Epinephrine; Heart; Injections, Intraperitoneal; Nitrendipine; Norepinephrine; Poisoning; Rats; Rats, Inbred Strains | 1991 |
Inhibition by cocaine of excitation-contraction coupling in isolated cardiomyocytes.
Topics: Animals; Calcium; Cell Separation; Cocaine; Dose-Response Relationship, Drug; Electric Conductivity; Heart; Lidocaine; Membrane Potentials; Myocardial Contraction; Myocardium; Nitrendipine; Potassium; Rats; Rats, Inbred Strains; Sarcoplasmic Reticulum; Sodium Channels; Sympathetic Nervous System; Tetrodotoxin; Verapamil | 1991 |
Effects of nitrendipine on cocaine-induced toxicity evaluated in primary myocardial cell cultures.
Topics: Animals; Cell Survival; Cocaine; Heart; In Vitro Techniques; L-Lactate Dehydrogenase; Myocardium; Nitrendipine; Rats; Rats, Inbred Strains | 1991 |
[Prevention of the cardiotoxicity of cocaine using a calcium blocker].
Topics: Animals; Cardiomyopathies; Cocaine; Nifedipine; Nitrendipine; Rats; Rats, Inbred Strains | 1985 |
A calcium-channel blocker as antidote to the cardiac effects of cocaine intoxication.
Topics: Animals; Arrhythmias, Cardiac; Calcium Channel Blockers; Cocaine; Dogs; Nifedipine; Nitrendipine; Rats | 1985 |
Nitrendipine: an antidote to cardiac and lethal toxicity of cocaine.
Topics: Animals; Arrhythmias, Cardiac; Blood Pressure; Cocaine; Drug Interactions; Heart; Heart Rate; Nitrendipine; Rats; Time Factors | 1986 |