Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Oleoylethanolamide (N-Oleoylethanolamide) is a high affinity endogenous agonist of PPAR-α.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
2 mg | In stock | $ 39.00 | |
5 mg | In stock | $ 64.00 | |
10 mg | In stock | $ 97.00 | |
25 mg | In stock | $ 189.00 | |
50 mg | In stock | $ 347.00 | |
100 mg | In stock | $ 555.00 | |
200 mg | In stock | $ 772.00 | |
500 mg | In stock | $ 1,180.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 70.00 |
Description | Oleoylethanolamide (N-Oleoylethanolamide) is a high affinity endogenous agonist of PPAR-α. |
In vitro | In vitro studies showed that OEA inhibited transforming growth factor β1-stimulated HSCs activation through suppressing Smad2/3 phosphorylation, α-SMA expression and myofibroblast transformation. |
In vivo | Treatment with OEA (5 mg/kg/day, intraperitoneal injection, i.p.) significantly attenuated the progress of liver fibrosis in both two experimental animal models by blocking the activation of hepatic stellate cells (HSCs).?Gene expression analysis of hepatic tissues indicated that OEA inhibited the expression of α-smooth muscle action (α-SMA) and collagen matrix, fibrosis markers, and genes involved in inflammation and extracellular matrix remodeling. |
Synonyms | N-Oleoylethanolamide, Oleamide MEA, Oleic acid monoethanolamide |
Molecular Weight | 325.53 |
Formula | C20H39NO2 |
CAS No. | 111-58-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: < 0.1 mg/mL (insoluble)
DMSO: 19.83 mg/mL (60.92 mM), Sonification is recommended.
You can also refer to dose conversion for different animals. More
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Oleoylethanolamide 111-58-0 DNA Damage/DNA Repair Metabolism Endogenous Metabolite PPAR N-Oleoylethanolamide Inhibitor inhibit Oleamide MEA Peroxisome proliferator-activated receptors Oleic acid monoethanolamide inhibitor