
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥365 | 有现货 |
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5MG | ¥583 | 有现货 |
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10MG | ¥875 | 有现货 |
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25MG | ¥1693 | 有现货 |
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50MG | ¥3183 | 有现货 |
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100MG | ¥4739 | 有现货 |
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500MG | ¥10287 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称AZD2858
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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
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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。
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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.
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体外实验——
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体内实验——
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同义词AZD-2858 | AZD 2858 | AZD2858
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通路PI3K/Akt/mTOR signaling
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靶点GSK-3
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受体GSK-3
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研究领域Other Indications
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适应症——
化学信息
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CAS Number486424-20-8
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分子量453.52
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分子式C21H23N7O3S
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纯度>98% (HPLC)
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溶解度DMSO: 7 mg/mL (15.43 mM)
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SMILESNC1=NC=C(C2=CC=C(S(N3CCN(C)CC3)(=O)=O)C=C2)N=C1C(NC4=CC=CN=C4)=O
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化学全称3-amino-6-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]-N-3-pyridinyl-2-pyrazinecarboxamid
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Sisask G, et al. Bone, 2013, 54(1), 126-132.
产品手册




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