BAY-0069,98.07%

产品编号:Bellancom-148351| CAS NO:420826-65-9| 分子式:C22H16BrN3O4| 分子量:466.28

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-148351
1000.00 杭州 北京(现货)
Bellancom-148351
1600.00 杭州 北京(现货)
Bellancom-148351
3500.00 杭州 北京(现货)
Bellancom-148351
5500.00 杭州 北京(现货)
Bellancom-148351
8500.00 杭州 北京(现货)

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BAY-0069

产品介绍 BAY-0069 是一种有效且具有选择性的 PPARγ 反向激活剂,对人 PPARγ 和鼠 PPARγ 的 IC50 分别为 6.3 nM 和 24 nM。BAY-0069 可用于癌症的研究。
生物活性

BAY-0069 is a potent and selective PPARγ inverse agonist with an IC50 value of 6.3 nM and 24 nM for human PPARγ and mouse PPARγ. BAY-0069 can be used to research cancer.

体外研究

BAY-0069 inhibits CYP2C8 with an IC50 of 4.3 μM.
BAY-0069 (0.1 nM-1 μM; 7 days) leads to antiproliferative effects in the PPARγ-amplified cell line UM-UC-9.

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

Cell Proliferation Assay

Cell Line: PPARγ-amplified cell line UM-UC-9
Concentration: 0.0001, 0.001, 0.01, 0.01 and 1 μM
Incubation Time: 7 days
Result: Inhibited PPARγ-amplified cell line UM-UC-9 with an IC50 of 2.54 nM.
体内研究
(In Vivo)

BAY-0069 (1 μM; 1 h) exhibits excellent microsomal stability with CLb,hmic of 0.47 L/h/kg in human liver microsomes and CLb,rhep of 3.9 L/h/kg in rat liver hepatocytes.
Pharmacokinetic Parameters of BAY-0069 in female NMRI nu/nu mice.

Route P.O. (100 mg/kg) I.P. S.C.
AUC0-tlast (mg/L·h) 0.074 0.26 0.045
Cmax (nM) 35 59 4.4

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

体内研究

BAY-0069 (1 μM; 1 h) exhibits excellent microsomal stability with CLb,hmic of 0.47 L/h/kg in human liver microsomes and CLb,rhep of 3.9 L/h/kg in rat liver hepatocytes.
Pharmacokinetic Parameters of BAY-0069 in female NMRI nu/nu mice.

Route P.O. (100 mg/kg) I.P. S.C.
AUC0-tlast (mg/L·h) 0.074 0.26 0.045
Cmax (nM) 35 59 4.4

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

体内研究

BAY-0069 (1 μM; 1 h) exhibits excellent microsomal stability with CLb,hmic of 0.47 L/h/kg in human liver microsomes and CLb,rhep of 3.9 L/h/kg in rat liver hepatocytes.
Pharmacokinetic Parameters of BAY-0069 in female NMRI nu/nu mice.

Route P.O. (100 mg/kg) I.P. S.C.
AUC0-tlast (mg/L·h) 0.074 0.26 0.045
Cmax (nM) 35 59 4.4

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

性状Solid
溶解性数据
In Vitro: 

DMSO : 100 mg/mL (214.46 mM; ultrasonic and warming and heat to 60°C)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.1446 mL 10.7232 mL 21.4463 mL
5 mM 0.4289 mL 2.1446 mL 4.2893 mL
10 mM 0.2145 mL 1.0723 mL 2.1446 mL
*

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。

运输条件

Room temperature in continental US; may vary elsewhere.

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

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