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  • (±)19(20)-EDP Ethanolamide
(±)19(20)-EDP Ethanolamide的可视化放大

(±)19(20)-EDP Ethanolamide

An ω-3 endocannabinoid epoxide and CB receptor agonist

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(±)19(20)-EDP Ethanolamide的二维码
  • 库存: 现货
可选规格
  • 包装
    价格
    促销价
    数量
  • 25ug
    ¥675.00
    540.00
    - +
  • 50ug
    ¥1287.00
    1030.00
    - +
  • 100ug
    ¥2450.00
    1960.00
    - +
  • 500ug
    ¥10837.00
    8670.00
    - +
已选 0 0
金额: ¥0.00
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  • 货号: ajci67552
  • CAS: 2123485-34-5
  • 别名: 19,20-DHEA epoxide, 19,20-epoxy Docosapentaenoic Acid Ethanolamide, 19,20-EDP-EA, 19,20-EDP epoxide
  • 分子式: C24H37NO3
  • 分子量: 387.6
  • 纯度: >98%
  • 溶解度: DMF: 50 mg/ml,DMSO: 50 mg/ml,Ethanol: 50 mg/ml,Ethanol:PBS(pH 7.2) (1:1): 0.5 mg/ml
  • 储存: Store at -20°C
  • 库存: 现货

Background

(±)19(20)-EDP ethanolamide is an ω-3 endocannabinoid epoxide and cannabinoid (CB) receptor agonist (EC50s = 108 and 280 nM for CB1 and CB2, respectively). It is produced through direct epoxygenation of docosahexaenoyl ethanolamide by cytochrome P450 (CYP) epoxygenases. (±)19(20)-EDP ethanolamide (25 µM) reduces the viability of 143B metastatic osteosarcoma cells. It decreases the production of IL-6 and increases the production of IL-10 when used at concentrations ranging from 2.5 to 10 µM in BV-2 microglia stimulated by LPS and decreases LPS-induced cytotoxicity when used at concentrations ranging from 5 to 10 µM. It also decreases nitrite production when used at a concentration of 7.5 µM, an effect that can be partially reversed by the CB2 receptor antagonist AM630 and the PPARγ antagonist GW 9662 . (±)19(20)-EDP ethanolamide induces vasodilation of isolated preconstricted bovine coronary arteries (ED50 = 1.9 µM) and reduces tube formation by human microvascular endothelial cells (HMVECs) in a Matrigel? assay.

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