• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

AZD2858

CAS No. 486424-20-8

AZD2858 ( AZD-2858 | AZD 2858 | AZD2858 )

产品货号. M14628 CAS No. 486424-20-8

AZD2858 是一种选择性 GSK-3 抑制剂,IC50 为 68 nM,抑制 S396 位点的 tau 磷酸化,激活 Wnt 信号通路。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥365 有现货
5MG ¥583 有现货
10MG ¥875 有现货
25MG ¥1693 有现货
50MG ¥3183 有现货
100MG ¥4739 有现货
500MG ¥10287 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    AZD2858
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    AZD2858 是一种选择性 GSK-3 抑制剂,IC50 为 68 nM,抑制 S396 位点的 tau 磷酸化,激活 Wnt 信号通路。
  • 产品描述
    AZD2858 is a selective GSK-3 inhibitor with an IC50 of 68 nM, inhibits tau phosphorylation at the S396 site, activates Wnt signaling pathway.(In Vitro):AZD2858 (1 μM) increases β-catenin levels after a short period of time in human osteoblast cells. AZD2858 inhibits GSK-3β dependent phosphorylation with an IC50 of 68 nM. AZD2858 (10 nM) has no effect on β-catenin levels. AZD2858 increases TAZ expression and osterix expression both by 1.4-fold, with EC50 of 440 nM and 1.2 μM, respectively, in hADSC. AZD2858 also induces a marked increase in osteogenic mineralisation in hADSC. AZD2858 (AR28) demonstrates from 70- to greater than 6000-fold selectivity over a panel of other kinases and an IC50 of 5 nM. AR28 inhibits GSK-3 in murine cells and indicates activation of the canonical Wnt/β-catenin signaling cascade. AR28 (50, 10, and 1 nM) enhances the clonogenic ability of mesenchymal progenitors with osteogenic and adipogenic potential. AR28 (50 μM) also enhances the differentiation ability of mesenchymal progenitors to the osteogenic but not adipogenic lineage in vitro. (In Vivo):AZD2858 (20 mg/kg) causes a dose-dependent increase in trabecular bone mass compared to control after a two-week treatment with a maximum effect. AZD2858 exhibits a substantial effect on fracture healing. AZD2858 (20 mg/kg) causes an increase in cortical BMC of 9%, cortical area of 10%, and cortical thickness of 11% at 3 weeks in the non-operated right femur of rats. AZD2858 (30 μmol/kg/day) alters the biomarkers of bone turnover with statistically significant increases in P1NP and decreases in TRAcP-5b seen from 3 days of treatment and onwards. AZD2858 demonstrates significant changes in serum bone turnover markers (P1NP and TRAcP-5b) and femur bone formation after only 7 days of daily dosing. AZD2858 (AR28, 30?mg/kg, s.c.) stimulates an increase in an initial wave of mesenchymal progenitors with osteogenic and adipogenic potential and drives their differentiation to the osteogenic lineage in BALB/c mice. AR28 (30?mg/kg, s.c.) enhances the proliferation of committed hematopoietic progenitors and their differentiation to the osteoclast lineage but does not prevent an overall increase in bone mass.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    AZD-2858 | AZD 2858 | AZD2858
  • 通路
    PI3K/Akt/mTOR signaling
  • 靶点
    GSK-3
  • 受体
    GSK-3
  • 研究领域
    Other Indications
  • 适应症
    ——

化学信息

  • CAS Number
    486424-20-8
  • 分子量
    453.52
  • 分子式
    C21H23N7O3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 7 mg/mL (15.43 mM)
  • SMILES
    NC1=NC=C(C2=CC=C(S(N3CCN(C)CC3)(=O)=O)C=C2)N=C1C(NC4=CC=CN=C4)=O
  • 化学全称
    3-amino-6-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]-N-3-pyridinyl-2-pyrazinecarboxamid

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Sisask G, et al. Bone, 2013, 54(1), 126-132.
产品手册
关联产品
  • GSK-3β inhibitor 2

    GSK-3β抑制剂2是GSK-3β的BBB穿越和选择性抑制剂(IC50 = 1.1 nM)。 GSK-3β抑制剂2可用于阿尔茨海默病的研究。

  • GSK-3β inhibitor 1 (...

    GSK-3β 抑制剂 1 是一种糖原合成酶激酶 3β (GSK-3β) 抑制剂,具有很高的抗糖尿病功效。

  • GSK3β inhibitor II

    GSK3β inhibitor II 是 GSK3β 的抑制剂。GSK3β inhibitor II 可用于阿尔茨海默病 (AD) 的研究。