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Design and synthesis of novel opioid ligands with an azabicyclo[2.2.2]octane skeleton and their pharmacologies
- Source :
- Bioorganic & Medicinal Chemistry Letters. 22:2689-2692
- Publication Year :
- 2012
- Publisher :
- Elsevier BV, 2012.
-
Abstract
- A novel opioid ligand possessing a stable and cyclic imine 16 and its derivatives with an azabicyclo[2.2.2]octane skeleton were synthesized. The imine 16 showed higher affinity for the μ receptor than compound 21 with an oxabicyclo[2.2.2]octane skeleton. Azabicyclo[2.2.2]octane derivative 18d with a cyclopropylmethyl group on the 8-nitrogen showed the highest affinity for the μ receptor among the synthesized derivatives.
- Subjects :
- μ receptor
Stereochemistry
Clinical Biochemistry
Imine
Receptors, Opioid, mu
Pharmaceutical Science
Ligands
Biochemistry
Bridged Bicyclo Compounds
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
medicine
Spiro Compounds
Molecular Biology
Octane
Aza Compounds
Molecular Structure
Ligand
Organic Chemistry
Octanes
Skeleton (computer programming)
Analgesics, Opioid
Morphinans
chemistry
Opioid
Drug Design
Receptors, Opioid
Molecular Medicine
Protein Binding
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....23436d482c815f138806d99d4f91e7ec
- Full Text :
- https://doi.org/10.1016/j.bmcl.2012.03.001