Powder: -20°C for 3 years | In solvent: -80°C for 1 year
20-HEPE is a metabolite of eicosapentaenoic acid that is formed via ω-oxidation of EPA by cytochrome P450 (CYP) ω-oxidases, including human CYP4F3B. It activates peroxisome proliferator-activated receptor α (PPARα) in COS-7 cells expressing a luciferase reporter when used at a concentration of 10 μM. 20-HEPE also activates murine transient receptor potential vanilloid receptor 1 (mTRPV1) in vitro but lacks antinociceptive activity in rats.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 μg | 35 days | $ 650.00 | |
50 μg | 35 days | $ 1,230.00 | |
100 μg | 35 days | $ 2,340.00 |
Description | 20-HEPE is a metabolite of eicosapentaenoic acid that is formed via ω-oxidation of EPA by cytochrome P450 (CYP) ω-oxidases, including human CYP4F3B. It activates peroxisome proliferator-activated receptor α (PPARα) in COS-7 cells expressing a luciferase reporter when used at a concentration of 10 μM. 20-HEPE also activates murine transient receptor potential vanilloid receptor 1 (mTRPV1) in vitro but lacks antinociceptive activity in rats. |
Molecular Weight | 318.457 |
Formula | C20H30O3 |
CAS No. | 116477-57-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMF: Miscible
DMSO: Miscible
PBS (pH 7.2): 0.8 mg/mL
Ethanol: Miscible
You can also refer to dose conversion for different animals. More
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20-HEPE 116477-57-7 20HEPE 20 HEPE inhibitor inhibit