Abstract
Selective CB2 receptor agonists are promising potential therapeutic agents for the treatment of inflammatory and neuropathic pain. A focused screen identified a pyrimidine ester as a partial agonist at the CB2 receptor with micromolar potency. Subsequent lead optimization identified 35, GW842166X, as the optimal compound in the series. 35 has an oral ED50 of 0.1 mg/kg in the rat FCA model of inflammatory pain and was selected as a clinical candidate for this indication.
MeSH terms
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Analgesics / chemical synthesis*
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Analgesics / pharmacokinetics
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Analgesics / pharmacology
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Animals
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Biological Availability
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Half-Life
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Humans
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Inflammation / drug therapy
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Inflammation / metabolism
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Pain / drug therapy*
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Pain / metabolism
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Pyrans / chemical synthesis*
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Pyrans / pharmacokinetics
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Pyrans / pharmacology
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Pyrimidines / chemical synthesis*
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Pyrimidines / pharmacokinetics
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Pyrimidines / pharmacology
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Rats
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Receptor, Cannabinoid, CB2 / agonists*
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Structure-Activity Relationship
Substances
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2-((2,4-dichlorphenyl)amino)-N-((tetrahydro-2H-pyran-4-yl)methyl)-4-(trifluoromethyl)-5-pyrimidinecarboxamide
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Analgesics
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Pyrans
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Pyrimidines
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Receptor, Cannabinoid, CB2