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M1069

    
≥98%

源叶(MedMol)
V47939 一键复制产品信息
3027658-65-4
C25H30N4O8S
546.59
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V47939-1mg
≥98%

¥2720.00

货期:3-5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: M1069 is a selective and orall active, dual A2A/A2B adenosine receptor antagonist with a selectivity of >100 fold against the A1 and A3 receptors. M1069 counteracts immune-suppressive mechanisms of adenosine, and exhibits anti-tumor activity.
靶点: A2AR,A2BR
体外研究: Metabolically stressful conditions, including inflammation and cancer, induces extracellular concentrations of adenosine increase.

M1069 dose-dependently suppresses 5’-N-ethylcarboxamide adenosine (stable analog of adenosine)-stimulated cyclic adenosine monophosphate (cAMP) and phosphorylated cAMP- response element binding protein (pCREB) induction, inhibits interleukin (IL)-2 production.

M1069 suppresses vascular endothelial growth factor (VEGF) production from human macrophages in adenosine-rich settings.

M1069 inhibits protumorigenic cytokine secretion, such as CXCL1, CXCL5 and granulocyte-colony stimulating factor, and reduces IL-12 secretion from adenosine-differentiated dendritic cells.

M1069 enhances T-cells activation in adenosine-differentiated dendritic cells.
体内研究: M1069 inhibits breast tumor (CD73hi/adenosine-rich 4T1 syngeneic) growth in vivo in mice and enhances chemotherapeutic agents efficacy.
保存条件: 2-8°C, 干燥
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.83 ml 9.148 ml 18.295 ml
5 mM 0.366 ml 1.83 ml 3.659 ml
10 mM 0.183 ml 0.915 ml 1.83 ml
50 mM 0.037 ml 0.183 ml 0.366 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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