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sdz ens 163 and arecoline

sdz ens 163 has been researched along with arecoline in 1 studies

*Arecoline: An alkaloid obtained from the betel nut (Areca catechu), fruit of a palm tree. It is an agonist at both muscarinic and nicotinic acetylcholine receptors. It is used in the form of various salts as a ganglionic stimulant, a parasympathomimetic, and a vermifuge, especially in veterinary practice. It has been used as a euphoriant in the Pacific Islands. [MeSH]

*Arecoline: An alkaloid obtained from the betel nut (Areca catechu), fruit of a palm tree. It is an agonist at both muscarinic and nicotinic acetylcholine receptors. It is used in the form of various salts as a ganglionic stimulant, a parasympathomimetic, and a vermifuge, especially in veterinary practice. It has been used as a euphoriant in the Pacific Islands. [MeSH]

Compound Research Comparison

Studies
(sdz ens 163)
Trials
(sdz ens 163)
Recent Studies (post-2010)
(sdz ens 163)
Studies
(arecoline)
Trials
(arecoline)
Recent Studies (post-2010) (arecoline)
6101,11020271

Protein Interaction Comparison

ProteinTaxonomysdz ens 163 (IC50)arecoline (IC50)
Muscarinic acetylcholine receptor M2Homo sapiens (human)3.6
Muscarinic acetylcholine receptor M1Rattus norvegicus (Norway rat)1.011
Muscarinic acetylcholine receptor M3Rattus norvegicus (Norway rat)0.963
Muscarinic acetylcholine receptor M4Rattus norvegicus (Norway rat)0.963
Muscarinic acetylcholine receptor M5Rattus norvegicus (Norway rat)0.963
Muscarinic acetylcholine receptor M2Rattus norvegicus (Norway rat)0.9163
Muscarinic acetylcholine receptor M1Homo sapiens (human)0.115

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Amstutz, R; Boelsterli, J; Bolliger, G; Floersheim, P; Gammenthaler, H; Gmelin, G; Shapiro, G; Supavilai, P; Walkinshaw, M1

Other Studies

1 other study(ies) available for sdz ens 163 and arecoline

ArticleYear
Muscarinic activity of the thiolactone, lactam, lactol, and thiolactol analogues of pilocarpine and a hypothetical model for the binding of agonists to the m1 receptor.
    Journal of medicinal chemistry, 1992, Volume: 35, Issue:1

    Topics: Animals; Binding, Competitive; Crystallography; Guinea Pigs; Lactams; Male; Mice; Models, Biological; Parasympathomimetics; Pilocarpine; Rats; Rats, Inbred Strains; Receptors, Muscarinic; Stereoisomerism; Structure-Activity Relationship; Sulfhydryl Compounds

1992