Chemical Structure : DG041
CAS No.: 861238-35-9
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.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥880 | In stock | |
| 10 mg | ¥1280 | In stock | |
| 25 mg | ¥1980 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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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.
| 分子量 | 592.30 | |
| 分子式 | C23H15Cl4FN2O3S2 | |
| 外观性状 | Solid | |
| 储存条件 |
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| 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 |
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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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