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R162

    
99.50%

R162

源叶(MedMol)
S86071 一键复制产品信息
64302-87-0
C17H12O3
264.27538
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S86071-5mg买3赠1
99.50%

¥400.00

3 - - - -
S86071-10mg买3赠1
99.50%

¥660.00

5 - - - -
S86071-25mg买3赠1
99.50%

¥1360.00

4 - - - -
S86071-50mg买3赠1
≥98%

¥2460.00

货期:2-3天 - - - -
S86071-100mg
≥98%

¥3940.00

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: R162 is a potent inhibitor of glutamate dehydrogenase 1 (GDH1/GLUD1), with anti-cancer properties.
靶点: Dehydrogenase
体外研究: Inhibition of GDH1 activity by R162 treatment results in decreased intracellular fumarate levels, attenuated GPx activity, increased ROS levels, and reduced cell proliferation in H1299 and MDA-MB231 cells, which can be significantly rescued by methyl-α-KG treatment as well as by antioxidant NAC. R162 inhibits cell proliferation and tumor growth potential of human cancer cells
体内研究: R162 (30 mg/kg/day, i.p.) does not result in a significant histopathological change between the vehicle-treated and R162-treated groups, nor alters complete blood counts, or hematopoietic properties in xenograft tumor mouse models. R162 (20 mg/kg/day) results in significantly decreased tumor growth and masses in mice compared with control mice and effectively inhibits GDH1 activity in resected tumors from xenograft nude mice
参考文献: 1. Jin L, et al. Glutamate dehydrogenase 1 signals through antioxidant glutathione peroxidase 1 to regulate redox homeostasis and tumor growth. Cancer Cell. 2015 Feb 9;27(2):257-70.
溶解性: Soluble  in  DMSO、Ethanol、DMF
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.784 ml 18.92 ml 37.839 ml
5 mM 0.757 ml 3.784 ml 7.568 ml
10 mM 0.378 ml 1.892 ml 3.784 ml
50 mM 0.076 ml 0.378 ml 0.757 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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