Page last updated: 2024-08-16

trihexyphenidyl and dicyclomine

trihexyphenidyl has been researched along with dicyclomine in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bleich, S; Gulbins, E; Kornhuber, J; Reichel, M; Terfloth, L; Tripal, P; Wiltfang, J1
Bhattacharjee, AK; Evans, SA; Gordon, RK; Pervitsky, D; Pomponio, JW1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Choo, LK; Darroch, SA; Mitchelson, F1
Giachetti, A; Giraldo, E; Ladinsky, H; Montagna, E1
Nilvebrant, L; Sparf, B1

Reviews

1 review(s) available for trihexyphenidyl and dicyclomine

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016

Other Studies

5 other study(ies) available for trihexyphenidyl and dicyclomine

ArticleYear
Identification of new functional inhibitors of acid sphingomyelinase using a structure-property-activity relation model.
    Journal of medicinal chemistry, 2008, Jan-24, Volume: 51, Issue:2

    Topics: Algorithms; Animals; Cell Line; Cell Line, Tumor; Chemical Phenomena; Chemistry, Physical; Enzyme Inhibitors; Humans; Hydrogen-Ion Concentration; Molecular Conformation; Quantitative Structure-Activity Relationship; Rats; Sphingomyelin Phosphodiesterase

2008
Discovery of subtype selective muscarinic receptor antagonists as alternatives to atropine using in silico pharmacophore modeling and virtual screening methods.
    Bioorganic & medicinal chemistry, 2013, May-01, Volume: 21, Issue:9

    Topics: Atropine; Computer Simulation; Drug Discovery; Humans; Models, Molecular; Molecular Structure; Receptor, Muscarinic M1; Structure-Activity Relationship

2013
Prejunctional muscarine receptors in the rabbit ear artery differ from M1, M2 and M3 muscarine receptors.
    Naunyn-Schmiedeberg's archives of pharmacology, 1992, Volume: 345, Issue:3

    Topics: Animals; Arteries; Carbachol; Dicyclomine; Ear, External; Guinea Pigs; Heart Atria; Hexamethonium; Hexamethonium Compounds; Ileum; In Vitro Techniques; Kinetics; Muscarinic Antagonists; Muscle, Smooth; Neuromuscular Junction; Rabbits; Receptors, Muscarinic; Trihexyphenidyl

1992
Binding and functional profiles of the selective M1 muscarinic receptor antagonists trihexyphenidyl and dicyclomine.
    British journal of pharmacology, 1986, Volume: 89, Issue:1

    Topics: (4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride; Animals; Blood Pressure; Cyclohexanecarboxylic Acids; Decerebrate State; Dicyclomine; Electric Stimulation; In Vitro Techniques; Male; Pirenzepine; Rats; Rats, Inbred Strains; Receptors, Muscarinic; Trihexyphenidyl; Vagus Nerve

1986
Dicyclomine, benzhexol and oxybutynine distinguish between subclasses of muscarinic binding sites.
    European journal of pharmacology, 1986, Apr-09, Volume: 123, Issue:1

    Topics: Animals; Benzodiazepinones; Binding, Competitive; Cerebral Cortex; Cyclohexanecarboxylic Acids; Dicyclomine; Guinea Pigs; In Vitro Techniques; Male; Mandelic Acids; Parasympatholytics; Pirenzepine; Quinuclidinyl Benzilate; Receptors, Muscarinic; Time Factors; Trihexyphenidyl; Urinary Bladder

1986