Page last updated: 2024-08-24

xanomeline and (4-(m-chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium chloride

xanomeline has been researched along with (4-(m-chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium chloride in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Bymaster, FP; Calligaro, DO; Deeter, JB; Merritt, L; Mitch, CH; Olesen, PH; Peters, SC; Sauerberg, P; Sawyer, BD; Shannon, HE; Sheardown, MJ; Swedberg, MD; Ward, JS1
Christopoulos, A; Felder, CC; Leach, K; Nawaratne, V; Sexton, PM1
Chen, H; Hou, Y; Wang, D; Wang, H; Wang, S; Xu, J; Yao, Y; Zhao, L1

Other Studies

3 other study(ies) available for xanomeline and (4-(m-chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium chloride

ArticleYear
Functionally selective M1 muscarinic agonists. 3. Side chains and azacycles contributing to functional muscarinic selectivity among pyrazinylazacycles.
    Journal of medicinal chemistry, 1995, Sep-01, Volume: 38, Issue:18

    Topics: Animals; Bridged Bicyclo Compounds; Bridged Bicyclo Compounds, Heterocyclic; Cell Line; Male; Mice; Muscarinic Agonists; Pyrazines; Pyridines; Rats; Rats, Sprague-Dawley; Receptors, Muscarinic; Structure-Activity Relationship; Thiadiazoles

1995
Structural determinants of allosteric agonism and modulation at the M4 muscarinic acetylcholine receptor: identification of ligand-specific and global activation mechanisms.
    The Journal of biological chemistry, 2010, Jun-18, Volume: 285, Issue:25

    Topics: (4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride; Acetylcholine; Allosteric Site; Animals; Cricetinae; Humans; Ligands; Models, Biological; Mutagenesis; Mutagenesis, Site-Directed; Protein Binding; Pyridines; Receptor, Muscarinic M4; Receptors, G-Protein-Coupled; Signal Transduction; Structure-Activity Relationship; Thiadiazoles

2010
Structural Insights into M1 Muscarinic Acetylcholine Receptor Signaling Bias between Gαq and β-Arrestin through BRET Assays and Molecular Docking.
    International journal of molecular sciences, 2023, Apr-16, Volume: 24, Issue:8

    Topics: (4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride; Acetylcholine; beta-Arrestin 1; beta-Arrestin 2; beta-Arrestins; Energy Transfer; GTP-Binding Proteins; HEK293 Cells; Humans; Molecular Docking Simulation; Pilocarpine; Receptor, Muscarinic M1

2023