溶解性 | 25°C: DMSO 7 mg/mL; Water <1 mg/mL; Ethanol <1mg/mL |
存贮条件 | 储存温度-20°C |
产品介绍 | AZD2858是GSK-3抑制剂,能激活Wnt信号通路。 |
备注 | AZD2858 is a selective GSK-3 inhibitor with an IC50 of 68 nM, activating Wnt signaling, increases bone mass in rats. |
生化机理 | AZD2858 is a selective GSK-3 inhibitor with an IC50 of 68 nM, inhibits tau phosphorylation at the S396 site, activates Wnt signaling pathway. AZD2858 treatment (1 μM, 12 h) on primary isolated human osteoblast-like cells results in a 3-fold increase of β-catenin levels. AZD2858 causes β-catenin stabilisation in human and rat mesenchymal stem cells, stimulates hADSC commitment towards osteoblasts and osteogenic mineralisation in vitro |
别名 | 3-氨基-6-(4-((4-甲基-1-哌嗪基)磺酰基)苯基)-N-3-吡啶基-吡嗪甲酰胺;;AZD 2858;AZD-2858;3-amino-6-(4-((4-methyl-1-piperazinyl)sulfonyl)phenyl)-n-3-pyridinyl-pyrazinecarboxamide |
AZD2858,GSK-3抑制剂
AZD2858 (订货以英文为准)
编号:A126819
CAS号:486424-20-8
分子式:C21H23N7O3S
分子量:453.52
产品名称 | AZD2858 |
中文名称 | AZD2858,GSK-3抑制剂 |
CAS号 | 486424-20-8 |
分子式(M.F.) | C21H23N7O3S |
分子量(M.W.) | 453.52 |
储存条件 | -20°C储存 |
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