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首页-小分子抑制剂&激动剂-Nuclear Receptor/Transcription Factor-Pregnane X Receptor (PXR)-SR12813
SR12813

Chemical Structure : SR12813

CAS No.: 126411-39-0

SR12813 (SR-12813;SR 12813;GW 485801;GW-485801;GW485801)

货号: PC-42261Not For Human Use, Lab Use Only.

SR12813 (GW485801) is potent and efficacious pregnane X receptor (PXR) activator with EC50 of 200 and 700 nM for human and rabbit PXR, respectively.

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25 mg ¥1280 In stock
50 mg ¥1980 In stock
100 mg ¥2980 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

SR12813 (GW485801) is potent and efficacious pregnane X receptor (PXR) activator with EC50 of 200 and 700 nM for human and rabbit PXR, respectively.
SR12813 (GW485801) only shows weak activition for rat and mouse PXR.
SR12813 (GW485801) inhibits cholesterol synthesis (IC50=1.2 uM) with no effect on fatty acid synthesis, reduces cellular HMG-CoA reductase activity with IC50 of 0.85 uM.
SR12813 (GW485801) induce CYP3A expression in primary hepatocytes.

物理化学性质&存储条件

分子量 504.5336
分子式 C24H42O7P2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Phosphonic acid, P,P'-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]ethenylidene]bis-, P,P,P',P'-tetraethyl ester

参考文献

1. Jones SA, et al. Mol Endocrinol. 2000 Jan;14(1):27-39.

2. Berkhout TA, et al. J Biol Chem. 1996 Jun 14;271(24):14376-82.

3. Watkins RE, et al. Science. 2001 Jun 22;292(5525):2329-33.

4. Berkhout TA, et al. Atherosclerosis. 1997 Sep;133(2):203-12.

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