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Design, synthesis, and structure-activity relationship of tropane muscarinic acetylcholine receptor antagonists.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2009 Aug 27; Vol. 52 (16), pp. 5241-52. - Publication Year :
- 2009
-
Abstract
- Novel tropane derivatives were characterized as muscarinic acetylcholine receptor antagonists (mAChRs). Through optimization of the structure-activity relationship around the tropane scaffold, the quaternary ammonium salt 34 was identified as a very potent M(3) mAChR antagonist. The compound was functionally active and displayed greater than 24 h duration of action in a mouse model of bronchoconstriction.
- Subjects :
- Animals
Biological Availability
Biphenyl Compounds chemistry
Biphenyl Compounds pharmacology
Bridged Bicyclo Compounds, Heterocyclic chemistry
Bridged Bicyclo Compounds, Heterocyclic pharmacology
Bronchi drug effects
Bronchi physiology
Bronchoconstriction drug effects
CHO Cells
Calcium metabolism
Cricetinae
Cricetulus
Drug Design
Humans
In Vitro Techniques
Mice
Mice, Inbred BALB C
Muscarinic Antagonists chemistry
Muscarinic Antagonists pharmacology
Muscle Contraction
Muscle, Smooth drug effects
Muscle, Smooth physiology
Radioligand Assay
Rats
Receptor, Muscarinic M1 physiology
Receptor, Muscarinic M2 physiology
Receptor, Muscarinic M3 physiology
Stereoisomerism
Structure-Activity Relationship
Tropanes chemistry
Tropanes pharmacology
Biphenyl Compounds chemical synthesis
Bridged Bicyclo Compounds, Heterocyclic chemical synthesis
Muscarinic Antagonists chemical synthesis
Tropanes chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 52
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 19630384
- Full Text :
- https://doi.org/10.1021/jm900736e