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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
CP-533536 free acid
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
223488-57-1
- 规格:
1 mg/5 mg/10 mg/25 mg
| 规格: | 1 mg | 产品价格: | ¥800.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥2000.0 |
| 规格: | 10 mg | 产品价格: | ¥3200.0 |
| 规格: | 25 mg | 产品价格: | ¥5500.0 |
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Evatanepag
CAS No. : 223488-57-1
MCE 国际站:Evatanepag
产品活性:Evatanepag (CP-533536) 是一种非前列腺素的,有效的和选择性的 EP2 受体 激动剂。 Evatanepag 可诱导局部骨形成 (in vivo)。Evatanepag 可用于骨折、骨缺损、哮喘的研究。
研究领域:GPCR/G Protein
作用靶点:Prostaglandin Receptor
In Vitro: Evatanepag (10 nM, 30 min) inhibits hFcεRI-induced mast cells degranulation in a dose-dependent manner.
Evatanepag (0.1 nM-10 μM, 12 min) results in an equivalent increase in intracellular cAMP in HEK-293 cells, with an IC50 of 50 nM.
In Vivo: Evatanepag (0.3-3.0 mg/kg, directly injected into the marrow cavity of the tibia) promotes bone formation in rats.
Evatanepag (0.3, 3.0 mg/kg, intranasal administration, from day1 to day4) reduces HDM aeroallergen-induced increased RL response to methacholine in mice.
Evatanepag (1 mg/kg, intravenous injection) demonstrates high i.v. clearance (Cl: 56 mL/min/kg) and a short half-life (t1/2: 0.33 h).
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