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GSK682753A

    
≥98%

GSK682753A

源叶(MedMol)
S82881 一键复制产品信息
1334294-76-6
C23H21Cl3N2O3
479.78344
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S82881-5mg
≥98%

¥1150.00

货期:3-5天 - - - -
S82881-10mg
≥98%

¥1890.00

货期:3-5天 - - - -
S82881-25mg
≥98%

¥3200.00

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: GSK682753A is a selective and highly potent inverse agonist of the epstein-barr virus-induced receptor 2 (EBI2) with an IC50 of 53.6 nM
靶点: IC50: 53.6 nM (EBI2);Others
体外研究: GSK682753 is a selective and highly potent inverse agonist for murine as well as human EBI2 with inhibition of G protein-dependent signals as well as signals that are probably G protein-independent. In cAMP-response element-binding protein-based reporter and guanosine5'-3-O-(thio)-triphosphate (GTPγS) binding assays, the potency of this compound is 2.6-53.6 nM, and its inhibitory efficacy is 75%. GSK682753A dose-dependently inhibits EBI2 with an IC50of 53.6 nM. GSK682753A inhibits ERK phosphorylation, GTPγS binding, and cAMP-response element-binding protein activation with similar potency
参考文献: 1. Benned-Jensen T, et al. Ligand modulation of the Epstein-Barr virus-induced seven-transmembrane receptor EBI2: identification of a potent and efficacious inverse agonist. J Biol Chem. 2011 Aug 19;286(33):29292-302.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.084 ml 10.421 ml 20.843 ml
5 mM 0.417 ml 2.084 ml 4.169 ml
10 mM 0.208 ml 1.042 ml 2.084 ml
50 mM 0.042 ml 0.208 ml 0.417 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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