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Evatanepag
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Evatanepag图片
CAS NO:223488-57-1
包装与价格:
包装价格(元)
1 mg询价
5 mg询价
10 mg询价
25 mg询价
50 mg询价
100 mg询价
200 mg询价
500 mg询价
1 mL*10 mM(in DMSO)询价

CP-533536 free acid
2-[3-[N-(4-叔丁基苄基)-N-(吡啶-3-基磺酰基)氨基甲基]苯氧基]乙酸
Evatanepag 是一种 EP2 受体选择性前列腺素 E2 (PGE2) 激动剂,可诱导局部骨形成,EC50 为 0.3 nM。它在大鼠骨折愈合模型中以单剂量局部给药时表现出愈合骨折的能力。

产品描述

Evatanepag is an EP2 receptor selective prostaglandin E2 (PGE2) agonist that induces local bone formation with EC50 of 0.3 nM.CP-533536 demonstrated the ability to heal fractures when administered locally as a single dose in rat models of fracture healing.

体外活性

CP-533536 is a potent and selective EP2agonist. CP-533536 shows the ability to heal fractures when administered locally as a single dose in rat models of fracture healing s excellent in vitro potency and it also displays against EP2 and selectivity against a broad panel of other targets.

Cas No.

223488-57-1

分子式

C25H28N2O5S

分子量

468.57

别名

CP-533536 free acid;2-[3-[N-(4-叔丁基苄基)-N-(吡啶-3-基磺酰基)氨基甲基]苯氧基]乙酸

储存和溶解度

DMSO:32 mg/mL (68.29 mM)
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
 
 
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