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INH1 (IBT13131)

    
99.70%

N-[4-(2,4-Dimethylphenyl)-2-thiazolyl]benzamide

源叶(MedMol)
S80623 一键复制产品信息
313553-47-8
C18H16N2OS
308.4
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S80623-2mg买3赠1
99.70%

¥80.00

4 - - - -
S80623-5mg买3赠1
99.70%

¥100.00

6 - - - -
S80623-10mg促销
99.70%

¥180.00 ¥144.00

6 - - - -
S80623-25mg促销
99.70%

¥350.00 ¥280.00

6 - - - -
S80623-50mg促销
99.70%

¥610.00 ¥488.00

5 - - - -
S80623-100mg促销
99.70%

¥1100.00 ¥880.00

4 - - - -
S80623-200mg促销
≥99%

¥2100.00 ¥1680.00

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: INH1 specifically disrupts the Hec1/Nek2 interaction via direct Hec1 binding. INH1 shows promising cancer inhibition activity both in vitro and in vivo
靶点: Apoptosis;Apoptosis;MicrotubuleAssociated
体内研究: INH1 (50 or 100 mg/kg, i.p., every other day/25 cycles) inhibits tumor outgrowth in a xenografted breast cancer model in nude mice
参考文献: 1. Wu G, et al. Small molecule targeting the Hec1/Nek2 mitotic pathway suppresses tumor cell growth in culture and in animal. Cancer Res. 2008 Oct 15;68(20):8393-9. 2. Shilong Zheng, et al. Discovery of a Series of Thiazole Derivatives as Novel Inhibitors of Metastatic Cancer Cell Migration and Invasion. ACS Med Chem Lett. 2013 Feb 14; 4(2): 191–196. 3. Yongxia Zhu, et al. Small Molecule TH-39 Potentially Targets Hec1/Nek2 Interaction and Exhibits Antitumor Efficacy in K562 Cells via G0/G1 Cell Cycle Arrest and Apoptosis Induction. Cell Physiol Biochem. 2016;40(1-2):297-308.
溶解性: DMSO  :  100  mg/mL  (324.25  mM;  Need  ultrasonic)
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.243 ml 16.213 ml 32.425 ml
5 mM 0.649 ml 3.243 ml 6.485 ml
10 mM 0.324 ml 1.621 ml 3.243 ml
50 mM 0.065 ml 0.324 ml 0.649 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

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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