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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T12296 | Oleoylethanolamide | N-Oleoylethanolamide,Oleamide MEA,Oleic acid monoethanolamide | Endogenous Metabolite , PPAR |
Oleoylethanolamide (N-Oleoylethanolamide) is a high affinity endogenous agonist of PPAR-α. | |||
T29938 | AM-3102 | KDS-5104,AM 3102,Methyl oleoylethanolamide | |
AM-3102 is an OEA analog that stimulates PPARα transcriptional activity and prolongs feeding latency. It is resistant to enzymatic hydrolysis and is as potent as OEA in enhancing transcriptional activity of PPARα and red... | |||
T25366 | Elaidyl-sulfamide | Elaidylsulfamide,ES | |
Elaidyl-sulfamide is a sulfamoyl analogue of oleoylethanolamide (OEA). ES is a lipid mediator of satiety that acts through the PPARα. | |||
T23204L | PSN 375963 hydrochloride(388575-52-8 Free base) | ||
PSN 375963 hydrochloride, a potent GPR119 agonist, demonstrates EC50 values of 8.4 μM and 7.9 μM for human and mouse GPR119, respectively. Its efficacy is comparable to that of the endogenous agonist oleoylethanolamide (... | |||
T60378 | NAAA-IN-2 | ||
NAAA-IN-2 (Compound 9), a potent and selective inhibitor of NAAA, exhibits an IC50 of 50 nM. NAAA, a cysteine amidase, primarily breaks down the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanolamide (OE... | |||
T60767 | NAAA-IN-1 | ||
NAAA-IN-1 (Compound 1) can be used in the inflammation and pain research. NAAA-IN-1 is a potent and selective NAAA inhibitor (IC 50 = 7 nM). NAAA is a cysteine amidase. NAAA preferentially hydrolyzes the endogenous bioli... | |||
T60432 | NAAA-IN-3 | ||
NAAA-IN-3 (Compound 17a) is a potent and selective NAAA inhibitor with an IC50 of 50 nM. NAAA is a cysteine amidase which preferentially hydrolyzes the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanola... |