E7046
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 10mg | ¥1395.00 | 现货 | |
| 25mg | ¥2590.00 | 现货 | |
| 50mg | ¥4583.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
E7046 is a potent and selective antagonist that potently competes with PGE2 binding to the type 4 prostaglandin E2 (PGE2) receptor EP4 [1,2].
Prostaglandin E2 receptor 4 (EP4) is a prostaglandin receptor for prostaglandin E2 (PGE2) implicated in various physiological and pathological responses in animal models and humans [3].
In vivo: In APCMin/+ mice, daily oral administration of E7046 slowed down the growth of established subcutaneous tumors and significantly delayed the recurrence of tumors after surgical resection. E7046 significantly reduced the combined colon polyp area and the size of individual polyps without influencing the total polyp number. E7046 exhibited great activity against colon and small intestine tumors [1]. E7046 delayed the growth of multiple syngeneic murine tumor types. E7046 showed no effect on tumor cell viability in vitro [2]. In the CT26 model, treatment with E7046 and anti-PD1 inhibited tumor growth. In the 4T1 model, E7046 in combination with anti-CTLA4 resulted in a nearly complete tumor growth inhibition [4].
References:
[1] Albu D I, Wu J, Huang K, et al. Abstract B198: Pharmacological profile of the PGE2 EP4 receptor antagonist E7046[J]. 2015.
[2] Albu D I, Huang K C, Wu J, et al. Abstract B034: Preclinical immune antitumor activity of myeloid-targeting E7046 and Treg depleting E7777[J]. 2016.
[3] Negishi M, Sugimoto Y, Ichikawa A. Prostaglandin E receptors[J]. Journal of lipid mediators and cell signalling, 1995, 12(2-3): 379-391.
[4] Bao X, Albu D, Huang K C, et al. Combination of EP4 antagonist and checkpoint inhibitors promotes anti-tumor effector T cells in preclinical tumor models[J]. Journal for immunotherapy of cancer, 2015, 3(2): P350.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 1369489-71-3 |
| 分子式 | C22H18F5N3O4 |
| 分子量 | 483.4 |
| 小分子别名 | Palupiprant |
| 化学名称 | 4-[(1S)-1-[[[3-(difluoromethyl)-1-methyl-5-[3-(trifluoromethyl)phenoxy]-1H-pyrazol-4-yl]carbonyl]amino]ethyl]-benzoic acid |
| 溶解度 | ≤12mg/ml in ethanol;14mg/ml in DMSO;2mg/ml in dimethyl formamide |
| SMILES | C[C@@H](c(cc1)ccc1C(O)=O)NC(c(c(C(F)F)n[n]1C)c1Oc1cccc(C(F)(F)F)c1)=O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | Palupiprant(E7046)是一种口服生物活性特异性 EP4 拮抗剂,IC50 为 13.5 nM,Ki 为 23.14 nM。Palupiprant 具有抗肿瘤活性。 |



沪公网安备 31011002003500