5,15-DPP
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 25mg | 请咨询 | 10-15工作日发货 | |
| 50mg | 请咨询 | 10-15工作日发货 | |
| 100mg | 请咨询 | 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
5,15-diphenylporphyrin (5,15-DPP) is a selective STAT3-SH2 antagonist [1].
Stat3 is constitutively activated in many human cancers. Stat3 functions as a critical mediator of oncogenic signaling through transcriptional activation of genes encoding apoptosis inhibitors, cell-cycle regulators and inducers of angiogenesis [2]. Aberrant STAT3 activity has been associated with transforming mechanisms induced by oncogenic tyrosine kinases [1].
In vitro: 5,15-DPP directly bound to STAT3 and antagonized the function of STAT3-SH2. 5,15-DPP selectively antagonized STAT3-SH2 with an IC50 of 0.28 μM over the other SH2-containing proteins STAT1 and Grb2[1]. The estimated KD values for the 5,15-DPP binding to STAT3 was 880 nM. Treatment with 5,15-DPP suppressed the DNA binding activity of STAT3 in a concentration-dependent manner. 5,15-DPP poorly inhibited STAT1 with an IC50 of 10 μM and showed no effect Grb2 [1].
References:
[1] Uehara Y, Mochizuki M, Matsuno K, et al. Novel high-throughput screening system for identifying STAT3–SH2 antagonists[J]. Biochemical and biophysical research communications, 2009, 380(3): 627-631.
[2] Jing N, Tweardy D J. Targeting Stat3 in cancer therapy[J]. Anti-cancer drugs, 2005, 16(6): 601-607.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 22112-89-6 |
| 分子式 | C32H22N4 |
| 分子量 | 462.6 |
| 小分子别名 | 5,15-Diphenylporphyrin |
| 化学名称 | 5,15-diphenyl-21H,23H-porphine |
| 溶解度 | ≤2mg/ml in dimethyl formamide |
| SMILES | c1c(/C=C(/C=C2)\N=C2/C(\c2ccccc2)=C(/C=C2)\N/C\2=C\C(C=C2)=N/C\2=C2/c3ccccc3)[nH]c/2c1 |
| 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 | 5,15-二苯基卟啉(5,15-DPP)是一种选择性 STAT3-SH2 拮抗剂(对 STAT3 和 STAT1 的 IC50 分别为 0.28 μM 和 10 μM)。 |



沪公网安备 31011002003500