Compounds > verapamil

verapamil and pirenzepine

verapamil has been researched along with pirenzepine in 12 studies

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	3 (25.00)	18.7374
1990's	1 (8.33)	18.2507
2000's	5 (41.67)	29.6817
2010's	3 (25.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Topliss, JG; Yoshida, F	1
Akamatsu, M; Fujikawa, M; Nakao, K; Shimizu, R	1
Du-Cuny, L; Mash, EA; Meuillet, EJ; Moses, S; Powis, G; Song, Z; Zhang, S	1
Akamatsu, M	1
Annand, R; Gozalbes, R; Jacewicz, M; Pineda-Lucena, A; Tsaioun, K	1
Cantin, LD; Chen, H; Kenna, JG; Noeske, T; Stahl, S; Walker, CL; Warner, DJ	1
Avenant, JC; Meyer, EC; Sommers, DK	1
Clementi, F; Gotti, C; Madeddu, L; Pandiella, A; Sher, E	1
Baumgold, J	1
Maggi, CA; Meli, A	1
Jankovic, SM; Jankovic, SV; Protic, BA	1
Mandryk, IuV; Skliarov, OIa	1

Trials

1 trial(s) available for verapamil and pirenzepine

Article	Year
Atropine and verapamil interactions in healthy volunteers. European journal of clinical pharmacology, 1991, Volume: 40, Issue:3 Topics: Adult; Atropine; Depression, Chemical; Drug Interactions; Heart Rate; Humans; Male; Pirenzepine; Single-Blind Method; Stimulation, Chemical; Verapamil	1991

Other Studies

11 other study(ies) available for verapamil and pirenzepine

Article	Year
QSAR model for drug human oral bioavailability. Journal of medicinal chemistry, 2000, Jun-29, Volume: 43, Issue:13 Topics: Administration, Oral; Biological Availability; Humans; Models, Biological; Models, Molecular; Pharmaceutical Preparations; Pharmacokinetics; Structure-Activity Relationship	2000
QSAR study on permeability of hydrophobic compounds with artificial membranes. Bioorganic & medicinal chemistry, 2007, Jun-01, Volume: 15, Issue:11 Topics: Biological Transport; Caco-2 Cells; Drug Evaluation, Preclinical; Humans; Hydrophobic and Hydrophilic Interactions; Membranes, Artificial; Permeability; Pharmaceutical Preparations; Quantitative Structure-Activity Relationship	2007
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
Importance of physicochemical properties for the design of new pesticides. Journal of agricultural and food chemistry, 2011, Apr-13, Volume: 59, Issue:7 Topics: Anabasine; Animals; Biological Availability; Cell Membrane Permeability; Chemical Phenomena; Drug Design; Humans; Imidazoles; Insecticides; Neonicotinoids; Nitro Compounds; Pesticides; Quantitative Structure-Activity Relationship; Receptors, Nicotinic	2011
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
Mitigating the inhibition of human bile salt export pump by drugs: opportunities provided by physicochemical property modulation, in silico modeling, and structural modification. Drug metabolism and disposition: the biological fate of chemicals, 2012, Volume: 40, Issue:12 Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Bile Acids and Salts; Cell Line; Chemical and Drug Induced Liver Injury; Humans; Quantitative Structure-Activity Relationship	2012
Intracellular calcium homeostasis in a human neuroblastoma cell line: modulation by depolarization, cholinergic receptors, and alpha-latrotoxin. Journal of neurochemistry, 1988, Volume: 50, Issue:6 Topics: Aminoquinolines; Arthropod Venoms; Atropine; Calcimycin; Calcium; Carbachol; Cytoplasm; Egtazic Acid; Fluorescent Dyes; Homeostasis; Humans; Ion Channels; Membrane Potentials; Neuroblastoma; Pirenzepine; Potassium Chloride; Receptors, Cholinergic; Receptors, Muscarinic; Receptors, Nicotinic; Spectrometry, Fluorescence; Spider Venoms; Tumor Cells, Cultured; Verapamil	1988
Effects of verapamil on the binding characteristics of muscarinic receptor subtypes. European journal of pharmacology, 1986, Jul-15, Volume: 126, Issue:1-2 Topics: Animals; Cerebral Cortex; In Vitro Techniques; Kinetics; Male; Medulla Oblongata; Myocardium; Pirenzepine; Pons; Rats; Rats, Inbred Strains; Receptors, Muscarinic; Verapamil	1986
Eserine-induced hypertone of guinea pig distal colon in vivo: a new pharmacological procedure for testing smooth muscle relaxants. Journal of pharmacological methods, 1984, Volume: 12, Issue:2 Topics: Animals; Atropine; Benzodiazepinones; Colon; Dicyclomine; Dose-Response Relationship, Drug; Guinea Pigs; Male; Methods; Muscle Contraction; Muscle, Smooth; Parasympatholytics; Physostigmine; Pirenzepine; Quaternary Ammonium Compounds; Verapamil	1984
Contractile effect of acetylcholine on isolated ampullar segment of Fallopian tubes. Pharmacological research, 2004, Volume: 49, Issue:1 Topics: Acetylcholine; Adult; Aged; Diamines; Fallopian Tubes; Female; Follicular Phase; Humans; Lidocaine; Luteal Phase; Mecamylamine; Menopause; Middle Aged; Muscle Contraction; Muscle, Smooth; Nifedipine; Piperidines; Pirenzepine; Verapamil	2004
[Blood circulation and secretory function in the gastric mucosa during inhibition of M1-cholinergic receptors and L-Ca2+-channels]. Fiziolohichnyi zhurnal (Kiev, Ukraine : 1994), 2005, Volume: 51, Issue:1 Topics: Animals; Calcium Channel Blockers; Calcium Channels, L-Type; Drug Synergism; Gastric Acid; Gastric Mucosa; Male; Muscarinic Antagonists; Pirenzepine; Rats; Rats, Wistar; Receptor, Muscarinic M1; Splanchnic Circulation; Verapamil	2005