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SC-1

    
97.60%

SC-1

源叶(MedMol)
S89007 一键复制产品信息
1313019-65-6
C21H13ClF3N3O2
431.795
N-[4-氯-3-(三氟甲基)苯基]-N′-[4-(4-氰基苯氧基)苯基]-脲
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89007-5mg买3赠1
97.60%

¥279.00

9 - - - -
S89007-10mg买3赠1
97.60%

¥340.00

10 - - - -
S89007-25mg买3赠1
97.60%

¥460.00

4 - - - -
S89007-100mg买3赠1
97.60%

¥1670.00

7 - - - -
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: SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib. SC-1 potently inhibits the phosphorylation of STAT3 by blocking STAT3 phosphorylation and activation, and induces apoptosis in hepatocellular carcinoma cell lines
靶点: Apoptosis; STAT;Apoptosis; STAT
体外研究: SC-1(1-10 μM; 48 hours; breast cancer cells) treatment demonstrates dose-dependent suppression of cell viability in all tested breast cancer cells. SC-1(1-10 μM; 36 hours; breast cancer cells) treatment induces potent apoptotic activity in association with downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines
体内研究: SC-1 showes efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors in vivo
细胞实验: Incubated HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells with 1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM SC-1 for 48 hours demonstrated that dose-dependent suppression of cell viability in all tested breast cancer cells. Incubated HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells with 1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM SC-1 for 36 hours showed downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines and induced potent apoptotic activity
动物实验: SC-1 (10 mg/kg; oral gavage; daily; for 28 days; Female NCr athymic nude mice (4-6 weeks of age) injected with breast cancer cells) treatment shows efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors
参考文献: 1. Chun-Yu Liu, et al. Novel sorafenib analogues induce apoptosis through SHP-1 dependent STAT3 inactivation in human breast cancer cells. Breast Cancer Res. 2013;15(4):R63.
溶解性: Soluble  in  DMSO
保存条件: 2-8°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.316 ml 11.58 ml 23.159 ml
5 mM 0.463 ml 2.316 ml 4.632 ml
10 mM 0.232 ml 1.158 ml 2.316 ml
50 mM 0.046 ml 0.232 ml 0.463 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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