Abstract
Ligand-based virtual screening led to the discovery of a new class of potent inverse agonists of the human cannabinoid receptor 1, hCB(1), which are selective versus hCB(2). These CB(1) ligands present intriguing departures from a classical CB(1) antagonist pharmacophore. Elements of SAR are discussed in this context.
MeSH terms
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Cannabinoids / chemical synthesis*
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Cannabinoids / chemistry
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Cannabinoids / pharmacology*
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Combinatorial Chemistry Techniques
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Drug Design
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Humans
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Ligands
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Molecular Structure
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Receptor, Cannabinoid, CB1 / agonists*
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Receptor, Cannabinoid, CB2 / agonists
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Structure-Activity Relationship
Substances
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Cannabinoids
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Ligands
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Receptor, Cannabinoid, CB1
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Receptor, Cannabinoid, CB2