2,3-Dihydro-1-Benzofuran Derivatives as a Series of Potent Selective Cannabinoid Receptor 2 Agonists: Design, Synthesis, and Binding Mode Prediction through Ligand-Steered Modeling
Autor: | Mohamed Naguib, Charles M. Thompson, Fanny Astruc-Diaz, Frank R. Fronczek, Jijun Xu, Philippe Diaz, Claudio N. Cavasotto, Sharangdhar S. Phatak |
---|---|
Rok vydání: | 2009 |
Předmět: |
Male
Models Molecular Stereochemistry CHO Cells Ligands Biochemistry Article Rats Sprague-Dawley Receptor Cannabinoid CB2 Structure-Activity Relationship Cricetulus Cricetinae Drug Discovery Cannabinoid receptor type 2 Animals Humans Structure–activity relationship Molecule General Pharmacology Toxicology and Pharmaceutics Receptor Benzofurans Pharmacology Molecular Structure Chemistry Ligand Organic Chemistry Analgesics Non-Narcotic Rats Hyperalgesia Asymmetric carbon Drug Design Molecular Medicine Racemic mixture Enantiomer |
Zdroj: | ChemMedChem. 4:1615-1629 |
ISSN: | 1860-7187 1860-7179 |
Popis: | We recently discovered and reported a series of N-alkyl-isatin acylhydrazone derivatives that are potent cannabinoid receptor 2 (CB(2)) agonists. In an effort to improve the druglike properties of these compounds and to better understand and improve the treatment of neuropathic pain, we designed and synthesized a new series of 2,3-dihydro-1-benzofuran derivatives bearing an asymmetric carbon atom that behave as potent selective CB(2) agonists. We used a multidisciplinary medicinal chemistry approach with binding mode prediction through ligand-steered modeling. Enantiomer separation and configuration assignment were carried out for the racemic mixture for the most selective compound, MDA7 (compound 18). It appeared that the S enantiomer, compound MDA104 (compound 33), was the active enantiomer. Compounds MDA42 (compound 19) and MDA39 (compound 30) were the most potent at CB(2). MDA42 was tested in a model of neuropathic pain and exhibited activity in the same range as that of MDA7. Preliminary ADMET studies for MDA7 were performed and did not reveal any problems. |
Databáze: | OpenAIRE |
Externí odkaz: |