Page last updated: 2024-08-17

carbachol and 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylic acid prop-2-ynyl ester

carbachol has been researched along with 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylic acid prop-2-ynyl ester in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bellucci, C; Buccioni, M; Dei, S; Gualtieri, F; Guandalini, L; Manetti, D; Martelli, C; Martini, E; Marucci, G; Matucci, R; Nesi, M; Romanelli, MN; Scapecchi, S; Teodori, E1
Bellucci, C; Buccioni, M; Cirilli, R; Dei, S; Guandalini, L; Manetti, D; Martini, E; Marucci, G; Matucci, R; Nesi, M; Romanelli, MN; Scapecchi, S; Teodori, E1

Other Studies

2 other study(ies) available for carbachol and 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylic acid prop-2-ynyl ester

ArticleYear
Highly chiral muscarinic ligands: the discovery of (2S,2'R,3'S,5'R)-1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide methyl iodide, a potent, functionally selective, M2 partial agonist.
    Journal of medicinal chemistry, 2006, Mar-23, Volume: 49, Issue:6

    Topics: Animals; Atrial Function, Left; CHO Cells; Cricetinae; Cricetulus; Cyclic S-Oxides; Guinea Pigs; Humans; Ileum; In Vitro Techniques; Ligands; Lung; Male; Muscle Contraction; Muscle, Smooth; Pyrrolidines; Rabbits; Receptor, Muscarinic M2; Stereoisomerism; Structure-Activity Relationship; Vas Deferens

2006
Synthesis and pharmacological characterization of chiral pyrrolidinylfuran derivatives: the discovery of new functionally selective muscarinic agonists.
    Journal of medicinal chemistry, 2008, Jul-10, Volume: 51, Issue:13

    Topics: Animals; CHO Cells; Circular Dichroism; Cricetinae; Cricetulus; Crystallography, X-Ray; Furans; Guinea Pigs; Humans; Lung; Male; Models, Molecular; Molecular Structure; Muscarinic Agonists; Pyrroles; Rabbits; Spectrophotometry; Stereoisomerism; Structure-Activity Relationship

2008