FPR2 agonist 2,99.59%

产品编号:Bellancom-144604| CAS NO:2829263-20-7| 分子式:C25H20F2N4O2| 分子量:446.45

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-144604
1500.00 杭州 北京(现货)
Bellancom-144604
2500.00 杭州 北京(现货)
Bellancom-144604
5500.00 杭州 北京(现货)
Bellancom-144604
9500.00 杭州 北京(现货)

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FPR2 agonist 2

产品介绍 FPR2 agonist 2 是一种有效的可透过血脑屏障的 FPR2 激动剂,h-FPR2EC50 值为 0.13 µM。FPR2 agonist 2 抑制促炎细胞因子的产生,抵消线粒体功能的变化,并抑制 caspase-3 的活性。
生物活性

FPR2 agonist 2 is a potent and permeates the blood−brain barrier FPR2 agonist with an EC50 of 0.13 µM, 1.1 µM for FPR2 and FPR1, respectively. FPR2 agonist 2 inhibits the production of pro-inflammatory cytokines, counterbalances the changes in mitochondrial function, and inhibits caspase-3 activity.

体外研究

FPR2 agonist 2 (compound (S)-11l) (1-100 µM; 48 h) exhibits low cytotoxicity with an EC50 value of 20.8 µM in N9 cells.
FPR2 agonist 2 (FPR1/FPR2 HL60 cells) shows agonist activity with EC50s of 0.13 µM, 1.1 µM (IC50s of 0.085 µM, Not determined) for FPR2 and FPR1, respectively.
FPR2 agonist 2 (0.1 µM) effectively blocks LPS-induced cell death and NO production and effectively suppresses the effect of LPS stimulation.
FPR2 agonist 2 (0.1 µM) counterbalances the changes in mitochondrial function, and inhibits caspase-3 activity.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: N9 cells
Concentration: 1-100 µM
Incubation Time: 48 h
Result: Exhibited low cytotoxicity with an EC50 value of 20.8 µM in N9 cells.
体内研究
(In Vivo)

FPR2 agonist 2 (1 mg/kg for i.v.; 10 mg/kg for i.p.) shows the ability to permeate the blood−brain barrier and to accumulate in the brain.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 25-30 g, male CD-1 mice
Dosage:
Administration: 1 mg/kg for i.v.; 10 mg/kg for i.p. (dissolved in 5% DMSO, 10% solutol HS 15, and 85% sterile water)
Result: Showed the ability to permeate the blood−brain barrier and to accumulate in the brain.
体内研究

FPR2 agonist 2 (1 mg/kg for i.v.; 10 mg/kg for i.p.) shows the ability to permeate the blood−brain barrier and to accumulate in the brain.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 25-30 g, male CD-1 mice
Dosage:
Administration: 1 mg/kg for i.v.; 10 mg/kg for i.p. (dissolved in 5% DMSO, 10% solutol HS 15, and 85% sterile water)
Result: Showed the ability to permeate the blood−brain barrier and to accumulate in the brain.
体内研究

FPR2 agonist 2 (1 mg/kg for i.v.; 10 mg/kg for i.p.) shows the ability to permeate the blood−brain barrier and to accumulate in the brain.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 25-30 g, male CD-1 mice
Dosage:
Administration: 1 mg/kg for i.v.; 10 mg/kg for i.p. (dissolved in 5% DMSO, 10% solutol HS 15, and 85% sterile water)
Result: Showed the ability to permeate the blood−brain barrier and to accumulate in the brain.
性状Solid
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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