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S82626

GSK 525768A

源叶(MedMol) 99%
  • 英文名:
  • GSK 525768A
  • 别名:
  • 2-[(4R)-6-(4-chlorophenyl)-1-methyl-8-(methyloxy)-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-N-ethylacetamide; CS-1255;
  • CAS号:
  • 1260530-25-3
  • 分子式:
  • C22H22ClN5O2
  • 分子量:
  • 423.8954
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源叶(MedMol) S82626-5mg 99% ¥2600.00元 预计交期:2-3天 - - - EA 加入购物车
源叶(MedMol) S82626-10mg 99% ¥4900.00元 预计交期:2-3天 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

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  • 产品描述: GSK 525768A is the inactive enantiomer of GSK525762A. GSK 525768A has no activity towards BET.
  • 靶点: Others
  • 体外研究:
    GSK 525768A has no activity towards BET. GSK 525768A (GSK525768A) is the (R)-enantiomer of GSK525762A. GSK525762A is shown to regulate levels of the high-density lipid protein apolipoprotein A1 (APOA1) in assays monitoring APOA1 release in liver cells, whereas the (R)-enantiomer (GSK 525768A) has no effect. GSK 525768A directly engages the protein module by forming hydrogen bonds with the conserved asparagine residue in a way that mimics the binding mode of acetylated lysine; this usually results in the binding of the inhibitor deeper within the acetylated lysine binding site but without displacing the conserved water molecules that are present at the bottom of the acetyl-lysine binding cavity
  • 参考文献:
    1. Nicodeme E, et al. Suppression of inflammation by a synthetic histone mimic. Nature. 2010 Dec 23;468(7327):1119-23. 2. Filippakopoulos P, et al. Targeting bromodomains: epigenetic readers of lysine acetylation. Nat Rev Drug Discov. 2014 May;13(5):337-56.
  • 溶解性: soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.359 ml 11.795 ml 23.591 ml
    5 mM 0.472 ml 2.359 ml 4.718 ml
    10 mM 0.236 ml 1.18 ml 2.359 ml
    50 mM 0.047 ml 0.236 ml 0.472 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)


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