HJC0197
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | ¥1090.00 | 10-15工作日发货 | |
| 10mg | ¥1745.00 | 10-15工作日发货 |
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
HJC0197 is a cell-permeable inhibitor of Epac1 and Epac2.
Exchange proteins directly activated by cAMP (Epac) are Rap1 guanine-nucleotide-exchange factor directly activated by cyclic AMP implicated in regulating a wide variety of intracellular processes in response to second messenger cAMP [1].
In vitro: HJC0197 showed an inhibitory effect against Epac2 with an IC50 value of 5.9 μM. In the presence of equal concentration of cAMP, HJC0197 inhibited Epac2 GEF activity to basal levels at 25 μM. HJC0197 also inhibited Epac1-mediated Rap1-GDP exchange activity at 25 μM in the presence of equal concentration of cAMP. HJC0197 was Epac-specific inhibitors that selectively blocked cAMP-induced Epac activation, but didn’t inhibit cAMP-mediated PKA activation. In HEK293/Epac1 and HEK293/Epac2 cells, pretreatment of with 10 μM HJC0197 for 5 min before the administration of 007-AM, a membrane permeable Epac selective agonist, completely blocked Epac1 and Epac2-mediated Akt phosphorylation [2]. In chicken micromass cultures, inhibition of the PKA-independent cAMP-mediators Epac1 and Epac2 with HJC0197 enhanced cartilage formation [3].
References:
[1]. De Rooij J, Zwartkruis F J T, Verheijen M H G, et al. Epac is a Rap1 guanine-nucleotide-exchange factor directly activated by cyclic AMP[J]. Nature, 1998, 396(6710): 474-477.
[2]. Chen H, Tsalkova T, Mei F C, et al. 5-Cyano-6-oxo-1, 6-dihydro-pyrimidines as potent antagonists targeting exchange proteins directly activated by cAMP[J]. Bioorganic & medicinal chemistry letters, 2012, 22(12): 4038-4043.
[3]. Juhász T, Matta C, Somogyi C, et al. Mechanical loading stimulates chondrogenesis via the PKA/CREB-Sox9 and PP2A pathways in chicken micromass cultures [J]. Cellular signaling, 2014, 26(3): 468-482.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 1383539-73-8 |
| 分子式 | C19H21N3OS |
| 分子量 | 339.5 |
| 化学名称 | 4-cyclopentyl-2-[[(2,5-dimethylphenyl)methyl]thio]-1,6-dihydro-6-oxo-5-pyrimidinecarbonitrile |
| 溶解度 | ≤5mg/ml in DMSO;10mg/ml in dimethyl formamide |
| SMILES | Cc1cc(CSC(NC(C2CCCC2)=C2C#N)=NC2=O)c(C)cc1 |
| 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 | HJC0197 是一种强效的 Epac1(由 cAMP 直接激活的交换蛋白 1)和 Epac2(Epac2 的 IC50=5.9 μM)拮抗剂。HJC0197 可选择性地阻断 cAMP 诱导的 Epac 激活。在等浓度的 cAMP 存在下,HJC0197 在 25 μM 时抑制 Epac1 介导的 Rap1-GDP 交换活性。 |
生物相关数据
质量控制
APExBIO 顾客使用本产品发表的 1 篇科研文献
- 1. Xue Song, Lugen Zuo, et al. "Rottlerin ameliorates DSS-induced colitis by improving intestinal barrier function via activation of the Epac-2/Rap-1 signaling pathway." Department of Central Laboratory.



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