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Discovery of novel 1-azoniabicyclo[2.2.2]octane muscarinic acetylcholine receptor antagonists
- Source :
- Journal of medicinal chemistry. 52(8)
- Publication Year :
- 2009
-
Abstract
- A novel 4-hydroxyl(diphenyl)methyl substituted quinuclidine series was discovered as a very promising class of muscarinic antagonists. The structure-activity relationships of the connectivity of the diphenyl moiety to the quinuclidine core and around the ring nitrogen side chain are described. Computational docking studies using an homology model of the M(3) receptor readily explained the observed structure-activity relationship of the various compounds. Compound 14o was identified as a very potent, slowly reversible M(3) antagonist with a very long in vivo duration of bronchoprotection.
- Subjects :
- Models, Molecular
Quinuclidines
Stereochemistry
Bronchoconstriction
Biological Availability
Bronchi
CHO Cells
In Vitro Techniques
chemistry.chemical_compound
Mice
Radioligand Assay
Structure-Activity Relationship
Cricetulus
In vivo
Cricetinae
Drug Discovery
Muscarinic acetylcholine receptor
Moiety
Animals
Humans
Homology modeling
Benzhydryl Compounds
Receptor
Receptor, Muscarinic M3
Chemistry
Antagonist
Muscle, Smooth
Bronchodilator Agents
Rats
Docking (molecular)
Molecular Medicine
Calcium
Quinuclidine
Muscle Contraction
Subjects
Details
- ISSN :
- 15204804
- Volume :
- 52
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Journal of medicinal chemistry
- Accession number :
- edsair.doi.dedup.....559c75618e50fb3c9a95e4bb3cec9dd2