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首页-小分子抑制剂&激动剂-GPCR-Prostaglandin Receptor-DG041
DG041

Chemical Structure : DG041

CAS No.: 861238-35-9

DG041 (DG-041)

货号: PC-27720Not For Human Use, Lab Use Only.

DG-041 (DG041) is a potent and selective prostanoid EP3 receptor antagonist with IC50 of 4.6 nM and 8.1 nM in binding and FLIPR assay, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

DG-041 (DG041) is a potent and selective prostanoid EP3 receptor antagonist with IC50 of 4.6 nM and 8.1 nM in binding and FLIPR assay, respectively.
DG-041 antagonized the effects of sulprostone on platelet function.
DG-041 potentiated the protective effects of PGE(2) on platelet aggregation by inhibiting the pro-aggregatory effect via EP3 stimulation.
DG041 (30 mg/kg) enhanced bladder capacity, inhibited the responses to GR63799X supporting the in vivo activity.

物理化学性质&存储条件

分子量 592.30
分子式 C23H15Cl4FN2O3S2
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

2,3-dichlorothiophene-5-sulfonic acid, 3-[1-(2,4-dichlorobenzyl)-5-fluoro-3-methyl-1H-indol-7-yl]acryloylamide

参考文献

1. Singh J, et al. J Med Chem. 2010 Jan 14;53(1):18-36.

2. Heptinstall S, et al. Platelets. 2008 Dec;19(8):605-13.

3. Jugus MJ, et al. Br J Pharmacol. 2009 Sep;158(1):372-81.

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