- 商品介绍
- 规格参数
- 包装参数
General description
一种可渗透细胞的氨基嘧啶化合物,可作为有效的,ATP竞争性和可逆的多激酶抑制剂(在≤ 10 µM ATP下,PDK1的IC50=11 nM;对于NUAK1,TBK1,MARK4,Aurora B,IKKε和PDK1,在100 µM ATP下,IC50=5、6、19、31、41和111 nM),并且显示出比Cdk2/E、EGFR、GSK-3β、IR、c-Kit、PKA、PKC、TAK1和VEGFR高50倍的选择性。显示可阻断PDK1/Akt信号传导,诱导PC-3和MDA-468细胞的生长停滞和凋亡(IC50分别为0.25和0.75 µM);此外,抑制IRF3的磷酸化(pSer396),核转位和转录活性,并减少刺激的巨噬细胞中IFN-β的产生。
Packaging
用惰性气体包装
Preparation Note
复溶后,等分并冷冻保存(-20°C)。储备液在-20°C条件下可稳定保存3个月。
Other Notes
Clark, K., et al. 2009.J. Biol. Chem.284, 14136.
Tamgumcy, T., et al. 2008.Exp.Cell Res.314, 2299.
Feldman, R.I., et al. 2005.J. Biol. Chem.280, 19867.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
毒性:标准处理(A)
| Quality Level | 100 |
| assay | ≥95% (HPLC) |
| form | solid |
| manufacturer/tradename | Calbiochem® |
| storage condition | OK to freeze,protect from light |
| color | pale yellow |
| solubility | DMSO: 50 mg/mL |
| shipped in | ambient |
| storage temp. | 2-8°C |
| SMILES string | Ic1c(nc(nc1)Nc3cc(ccc3)NC(=O)N4CCCC4)NCCCNC(=O)c2[s]ccc2 |
| InChI | 1S/C23H26IN7O2S/c24-18-15-27-22(30-20(18)25-9-5-10-26-21(32)19-8-4-13-34-19)28-16-6-3-7-17(14-16)29-23(33)31-11-1-2-12-31/h3-4,6-8,13-15H,1-2,5,9-12H2,(H,26,32)(H,29,33)(H2,25,27,28,30) |
| InChI key | VAVXGGRQQJZYBL-UHFFFAOYSA-N |
| 长度(mm) | |
| 宽度(mm) | |
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| 重量(kg) |





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