Abstract
A number of pyrazolopyrimidines were synthesized and tested for their positive allosteric modulation of the HCA(2) receptor (GPR109A). Compound 24, an efficacious and potent agonist and allosteric enhancer of nicotinic acid's action, was the basis for most other compounds. Interestingly, some of the compounds were found to increase the efficacy of the endogenous ligand 3-hydroxybutyrate and enhance its potency almost 10-fold. This suggests that the pyrazolopyrimidines may have therapeutic value when given alone.
© 2012 American Chemical Society
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3-Hydroxybutyric Acid / metabolism
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Allosteric Regulation
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Drug Synergism
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Guanosine 5'-O-(3-Thiotriphosphate) / pharmacology
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HEK293 Cells
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Humans
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Niacin / pharmacology
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Pyrazoles / chemical synthesis*
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Pyrazoles / chemistry
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Pyrazoles / pharmacology
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Pyrimidines / chemical synthesis*
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Pyrimidines / chemistry
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Pyrimidines / pharmacology
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Radioligand Assay
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Receptors, G-Protein-Coupled / agonists
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Receptors, G-Protein-Coupled / metabolism*
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Receptors, Nicotinic / metabolism*
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Structure-Activity Relationship
Substances
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HCAR2 protein, human
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Pyrazoles
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Pyrimidines
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Receptors, G-Protein-Coupled
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Receptors, Nicotinic
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Niacin
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Guanosine 5'-O-(3-Thiotriphosphate)
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3-Hydroxybutyric Acid