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SC 66

    
99.04%

SC 66

源叶(MedMol)
S86942 一键复制产品信息
871361-88-5
C18H16N2O
276.33
Cyclohexanone, 2,6-bis(4-pyridinylMethylene)-, (2E,6E)-;(2E,6E)-2,6-Bis(4-pyridinylmethylene)-cyclohexanone
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S86942-2mg买3赠1
99.04%

¥212.00

5 - - - -
S86942-5mg买3赠1
99.04%

¥374.00

5 - - - -
S86942-10mg买3赠1
99.04%

¥526.00

6 - - - -
S86942-25mg买3赠1
99.04%

¥930.00

6 - - - -
S86942-50mg买3赠1
99.04%

¥1380.00

5 - - - -
S86942-100mg买3赠1
99.04%

¥2020.00

5 - - - -
S86942-200mg买3赠1
≥99%

¥3500.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: SC66 is an Akt inhibitor, reduces cell viability in a dose- and time-dependent manner, inhibits colony formation and induces apoptosis in hepatocellular carcinoma (HCC) cells.
靶点: Akt;Apoptosis;Akt
体内研究: To demonstrate the effectiveness in vivo of SC66 on HCC, a mouse xenograft tumor model of Hep3B cells is used. When tumors became palpable, at a size of about 150 mm3, mice are randomized into three groups of 6 animals each. The treated group receive SC66 at 15 and 25 mg/kg twice a week via i.p. injection, while the untreated group receive the vehicle alone. Treatment with 25 mg/Kg SC66 significantly reduces tumor volume to 37% on day 17 when compared with tumors of the untreated group
参考文献: 1. Cusimano A, et al. Cytotoxic activity of the novel small molecule AKT inhibitor SC66 in hepatocellular carcinoma cells. Oncotarget. 2015 Jan 30;6(3):1707-22.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.619 ml 18.094 ml 36.189 ml
5 mM 0.724 ml 3.619 ml 7.238 ml
10 mM 0.362 ml 1.809 ml 3.619 ml
50 mM 0.072 ml 0.362 ml 0.724 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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