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R112

    
10mM in DMSO

R112

源叶(MedMol)
T98675 一键复制产品信息
575474-82-7
C16H13FN4O2
312.3
Phenol,3,​3'-​[(5-​fluoro-​2,​4-​pyrimidinediyl)​diimino]​bis-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T98675-1ml促销
10mM in DMSO

¥720.00 ¥648.00

6 - - - -
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: Syk抑制剂;Syk Inhibitors;;InformationR112 R112 is an ATP-competitive spleen tyrosine kinase (Syk) inhibitor with Ki value of 96 nM.TargetsSyk (Cell-free assay) 96 nM(Ki)In vitroR112 inhibits degranulation induced by anti-IgE cross-linking in mast cells (tryptase release, effective concentration for 50% inhibition [EC50] = 353 nmol/L) or basophils (histamine release, EC50 = 280 nmol/L), and by allergen (dust mite) in basophils (histamine release, EC50 = 490 nmol/L). R112 also blocks leukotriene C4 production and all proinflammatory cytokines tested. Its onset of action is immediate, and the inhibition is reversible. R112 is able to completely inhibit all three IgE-induced mast cell functions: degranulation, lipid mediator production, and cytokine production. R112 does not inhibit phosphorylation of the Lyn target Syk (Y352), but inhibits the phosphorylation of the Syk target LAT (Y191), indicating that Syk kinase is the primary target of R112. Most phosphorylation events downstream of Syk are inhibited with similar potency by R112. In vitro kinase assays do not always correlate with the corresponding activity inside cells. R112 inhibits the Lyn kinase in vitro assay with an IC50 of 0.3 μmol/L; however, as mentioned previously, in CHMCs (Cultured human mast cells), R112 does not inhibit the phosphorylation of Syk (Y352), and therefore most likely does not inhibit Lyn activity.
靶点: IC50: 226 nM (Syk kinase)
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.202 ml 16.01 ml 32.02 ml
5 mM 0.64 ml 3.202 ml 6.404 ml
10 mM 0.32 ml 1.601 ml 3.202 ml
50 mM 0.064 ml 0.32 ml 0.64 ml
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参考文献

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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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