Compounds > nitrendipine

nitrendipine and phencyclidine

nitrendipine has been researched along with phencyclidine in 9 studies

Research

Studies (9)

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

Authors	Studies
Bruno-Blanch, L; Gálvez, J; García-Domenech, R	1
Lombardo, F; Obach, RS; Waters, NJ	1
Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV	1
Du-Cuny, L; Mash, EA; Meuillet, EJ; Moses, S; Powis, G; Song, Z; Zhang, S	1
Annand, R; Gozalbes, R; Jacewicz, M; Pineda-Lucena, A; Tsaioun, K	1
Bolger, GT; Rafferty, MF; Skolnick, P	2
Bolger, GT; Rafferty, MF; Rice, KC; Skolnick, P; Weissman, BA	1
Pert, CB; Quirion, R	1

Other Studies

9 other study(ies) available for nitrendipine and phencyclidine

Article	Year
Topological virtual screening: a way to find new anticonvulsant drugs from chemical diversity. Bioorganic & medicinal chemistry letters, 2003, Aug-18, Volume: 13, Issue:16 Topics: Anticonvulsants; Computer Simulation; Databases, Factual; Discriminant Analysis; Drug Design; Molecular Structure; Quantitative Structure-Activity Relationship	2003
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds. Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:7 Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding	2008
Physicochemical determinants of human renal clearance. Journal of medicinal chemistry, 2009, Aug-13, Volume: 52, Issue:15 Topics: Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kidney; Metabolic Clearance Rate; Molecular Weight	2009
Computational modeling of novel inhibitors targeting the Akt pleckstrin homology domain. Bioorganic & medicinal chemistry, 2009, Oct-01, Volume: 17, Issue:19 Topics: Antineoplastic Agents; Blood Proteins; Caco-2 Cells; Cell Membrane Permeability; Computer Simulation; Drug Discovery; Drug Screening Assays, Antitumor; Humans; Models, Molecular; Phosphoproteins; Protein Binding; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-akt; Quantitative Structure-Activity Relationship	2009
QSAR-based permeability model for drug-like compounds. Bioorganic & medicinal chemistry, 2011, Apr-15, Volume: 19, Issue:8 Topics: Caco-2 Cells; Cell Membrane Permeability; Drug Discovery; Humans; Pharmaceutical Preparations; Pharmacokinetics; Quantitative Structure-Activity Relationship	2011
Phencyclidine increases the affinity of dihydropyridine calcium channel antagonist binding in rat brain. Naunyn-Schmiedeberg's archives of pharmacology, 1985, Volume: 330, Issue:3 Topics: Animals; Binding Sites; Brain; Calcium; Calcium Channel Blockers; Dihydropyridines; In Vitro Techniques; Kinetics; Magnesium; Male; Nifedipine; Nitrendipine; Phencyclidine; Pyridines; Rats; Rats, Inbred Strains	1985
Enhancement of brain calcium antagonist binding by phencyclidine and related compounds. Pharmacology, biochemistry, and behavior, 1986, Volume: 24, Issue:3 Topics: Anesthetics, Local; Animals; Binding Sites; Brain; Calcium Channel Blockers; Diltiazem; In Vitro Techniques; Male; Narcotics; Neurotoxins; Nifedipine; Nitrendipine; Phencyclidine; Rats; Rats, Inbred Strains	1986
Acylating phencyclidines irreversibly enhance brain calcium antagonist binding. Pharmacology, biochemistry, and behavior, 1986, Volume: 25, Issue:1 Topics: Animals; Brain; Male; Membranes; Mice; Mice, Inbred ICR; Nifedipine; Nitrendipine; Phencyclidine; Stimulation, Chemical	1986
Certain calcium antagonists are potent displacers of [3H]phencyclidine (PCP) binding in rat brain. European journal of pharmacology, 1982, Sep-10, Volume: 83, Issue:1-2 Topics: Animals; Binding, Competitive; Brain; Calcium Channel Blockers; Gallopamil; In Vitro Techniques; Nifedipine; Nitrendipine; Olfactory Bulb; Phencyclidine; Rats; Verapamil	1982