GPR109 receptor agonist-1 is a highly selective agonist of the human orphan G protein-coupled receptor GPR109b , and does not activate the mouse homologous receptor PUMA-G . GPR109 receptor agonist-1 functionally modulates the human GPR109b receptor via the cAMP signaling pathway, with an EC 50 of 400 nM. GPR109 receptor agonist-1 inhibits isoproterenol ( HY-B0468 )-stimulated lipolysis in human subcutaneous adipocytes, with efficacy comparable to that of Niacin ( HY-B0143 ), and does not act on β-adrenergic receptors. GPR109 receptor agonist-1 can be used in studies related to dyslipidemia and atherosclerosis.
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