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  3. FPR2 agonist 2

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。

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FPR2 agonist 2 Chemical Structure

FPR2 agonist 2 Chemical Structure

CAS No. : 2829263-20-7

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

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[1].

IC50 & Target

EC50: 0.13 µM (FPR2); 1.1 µM (FPR1)[1]

体外研究
(In Vitro)

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[1].
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[1].
FPR2 agonist 2 (0.1 µM) effectively blocks LPS-induced cell death and NO production and effectively suppresses the effect of LPS stimulation[1].
FPR2 agonist 2 (0.1 µM) counterbalances the changes in mitochondrial function, and inhibits caspase-3 activity[1].

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

Cell Viability Assay[1]

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[1].

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

Animal Model: 25-30 g, male CD-1 mice[1]
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.
分子量

446.45

Formula

C25H20F2N4O2

CAS 号
性状

固体

颜色

White to off-white

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
溶解性数据
In Vitro: 

DMSO 中的溶解度 : 50 mg/mL (111.99 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.2399 mL 11.1995 mL 22.3989 mL
5 mM 0.4480 mL 2.2399 mL 4.4798 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

FPR2 agonist 2 相关分类

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.2399 mL 11.1995 mL 22.3989 mL 55.9973 mL
5 mM 0.4480 mL 2.2399 mL 4.4798 mL 11.1995 mL
10 mM 0.2240 mL 1.1199 mL 2.2399 mL 5.5997 mL
15 mM 0.1493 mL 0.7466 mL 1.4933 mL 3.7332 mL
20 mM 0.1120 mL 0.5600 mL 1.1199 mL 2.7999 mL
25 mM 0.0896 mL 0.4480 mL 0.8960 mL 2.2399 mL
30 mM 0.0747 mL 0.3733 mL 0.7466 mL 1.8666 mL
40 mM 0.0560 mL 0.2800 mL 0.5600 mL 1.3999 mL
50 mM 0.0448 mL 0.2240 mL 0.4480 mL 1.1199 mL
60 mM 0.0373 mL 0.1867 mL 0.3733 mL 0.9333 mL
80 mM 0.0280 mL 0.1400 mL 0.2800 mL 0.7000 mL
100 mM 0.0224 mL 0.1120 mL 0.2240 mL 0.5600 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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FPR2 agonist 2
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HY-144604
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