AM3102 is a potent agonist of peroxisome proliferator-activated receptor alpha (PPAR-alpha). This endogenous high-affinity compound, an analog of oleoylethanolamide (OEA), is resistant to enzymatic hydrolysis, allowing for sustained activation of PPAR-alpha in vitro. Research demonstrates that AM3102 effectively reduces feeding behavior when administered both parenterally and orally, making it a valuable tool for studies on metabolism and appetite regulation.
AM3102 is a potent agonist of peroxisome proliferator-activated receptor alpha (PPAR-alpha). This endogenous high-affinity compound, an analog of oleoylethanolamide (OEA), is resistant to enzymatic hydrolysis, allowing for sustained activation of PPAR-alpha in vitro. Research demonstrates that AM3102 effectively reduces feeding behavior when administered both parenterally and orally, making it a valuable tool for studies on metabolism and appetite regulation.
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