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Structure-activity relationships of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of cough
- Source :
- Bioorganicmedicinal chemistry letters. 18(24)
- Publication Year :
- 2008
-
Abstract
- A series of 3-axial-aminomethyl-N-benzhydryl-nortropane analogs have been synthesized and identified to bind to the nociceptin receptor with high affinity. Many of these analogs showed high binding selectivity over classic opioid receptors such as μ receptor. The synthesis and structure–activity relationships around the C-3 nortropane substitution are described. Selected compounds with potent oral antitussive activity in the guinea pig model are disclosed.
- Subjects :
- Agonist
medicine.drug_class
Stereochemistry
Nortropanes
Chemistry, Pharmaceutical
Clinical Biochemistry
NOP
Guinea Pigs
Pharmaceutical Science
CHO Cells
Ligands
Biochemistry
Chemical synthesis
Nociceptin Receptor
Structure-Activity Relationship
Cricetulus
Cricetinae
Drug Discovery
medicine
Animals
Receptor
Molecular Biology
Binding selectivity
Chemistry
Ligand
Organic Chemistry
Nociceptin receptor
Kinetics
Opioid
Cough
Models, Chemical
Drug Design
Receptors, Opioid
Molecular Medicine
medicine.drug
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 18
- Issue :
- 24
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....fd2d9dc43b8d1288553c3e0222b9e75e