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Discovery of an opioid kappa receptor selective pure antagonist from a library of N-substituted 4beta-methyl-5-(3-hydroxyphenyl)morphans.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2002 Aug 01; Vol. 45 (16), pp. 3524-30. - Publication Year :
- 2002
-
Abstract
- A library of compounds biased toward opioid receptor antagonist activity was prepared by incorporating N-phenylpropyl-4beta-methyl-5-(3-hydroxyphenyl)morphans as the core scaffold using simultaneous solution phase synthetic methodology. From this library, N-phenylpropyl-4beta-methyl-5-(3-hydroxyphenyl)-7alpha-[3-(1-piperidinyl)propanamido]morphan [(-)-3b] was identified as the first potent and selective kappa opioid receptor antagonist from the 5-phenylmorphan class of opioids.
- Subjects :
- Animals
Brain metabolism
Bridged Bicyclo Compounds, Heterocyclic chemistry
Bridged Bicyclo Compounds, Heterocyclic pharmacology
CHO Cells
Combinatorial Chemistry Techniques
Cricetinae
Guinea Pigs
Humans
In Vitro Techniques
Ligands
Morphinans chemistry
Morphinans pharmacology
Radioligand Assay
Rats
Stereoisomerism
Structure-Activity Relationship
Bridged Bicyclo Compounds, Heterocyclic chemical synthesis
Morphinans chemical synthesis
Receptors, Opioid, kappa antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 45
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12139463
- Full Text :
- https://doi.org/10.1021/jm020084h