Abstract
Novel isoxazole carboxamides have been identified as growth hormone secretagogue receptor (GHS-R) antagonists. Substituent modification off the 5-position of the isoxazole ring led to analogues with potent binding affinity and functional antagonism of GHS-R. A potent analogue (32) with high aqueous solubility and good GPCR selectivity was also identified as a potential pharmacological tool for in vivo studies.
MeSH terms
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Amides / chemical synthesis*
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Amides / chemistry
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Amides / pharmacology
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Animals
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CHO Cells
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Cricetinae
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Cricetulus
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Humans
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Isoxazoles / chemical synthesis*
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Isoxazoles / chemistry
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Isoxazoles / pharmacology
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Mice
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Radioligand Assay
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Rats
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Receptors, G-Protein-Coupled / antagonists & inhibitors*
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Receptors, Ghrelin
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Solubility
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Stereoisomerism
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Structure-Activity Relationship
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Water
Substances
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Amides
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Isoxazoles
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Receptors, G-Protein-Coupled
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Receptors, Ghrelin
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Water