• 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

Alisertib

CAS No. 1028486-01-2

Alisertib ( MLN 8237 | MLN8237 | MLN-8237 )

产品货号. M10137 CAS No. 1028486-01-2

一种有效且高度选择性的 Aurora A 抑制剂,IC50 为 1.2 nM;对 Aurora B (IC50=396.5 nM) 和 205 激酶组的活性较低。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥405 有现货
10MG ¥713 有现货
25MG ¥1272 有现货
50MG ¥1928 有现货
100MG ¥3013 有现货
200MG ¥3872 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Alisertib
  • 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
    一种有效且高度选择性的 Aurora A 抑制剂,IC50 为 1.2 nM;对 Aurora B (IC50=396.5 nM) 和 205 激酶组的活性较低。
  • 产品描述
    A potent and highly selective inhibitor of Aurora A with IC50 of 1.2 nM; has less activity against Aurora B (IC50=396.5 nM) and a 205-kinase panel; inhibits proliferation of human tumor cell lines in vitro and produces tumor growth inhibition in solid tumor xenograft models.(In Vitro):Levetiracetam increases the transcription of HDACs and recruits corepressor complex on O6-Methylguanine-DNA-methyltransferase (MGMT) promoter, thus silencing its activity.Levetiracetam sensitizes (40 μg/mL) glioblastoma multiforme stem-like cells (GSCs) to Temozolomide (250 μM) treatment.MGMT expression is downregulated in GCSCs treated with Levetiracetam?(40 μg/mL).(In Vivo):Levetiracetam (10, 25, or 50?mg/kg) suppresses behavioral and electrographic seizure activity during neonatal hypoxia.
  • 体外实验
    Alisertib (MLN 8237) leads the MM cells to mitotic spindle abnormalities, mitotic accumulation, as well as inhibition of cell proliferation through apoptosis and senescence. Alisertib up-regulates p53 and tumor suppressor genes p21 and p27. The decreased activity of Alisertib (MLN 8237) for the T217D/W277E Aurora A/TPX2 complex may reflect the increased affinity for ATP induced by cofactor binding to Aurora A.Alisertib (MLN 8237) inhibits cell proliferation with IC50s ranging from 15 to 469 nM in different tumer cell lines.
  • 体内实验
    Alisertib (MLN 8237) (30 mg/kg, p.o.) significantly reduces tumor burden and increases overall survival in xenograft-murine model of human-MM.Alisertib (3-30 mg/kg; p.o.; once daily for 3 weeks) causes tumor growth inhibition in solid tumor xenograft models. Animal Model:Nude mice bearing HCT-116 colon tumor xenograft Dosage:3, 10, or 30 mg/kg Administration:P.o.; once daily for 3 weeks Result:Resulted in a dose-dependent TGI (tumor growth inhibition) of 43.3%, 84.2%, and 94.7% for the 3, 10, and 30 mg/kg groups,respectively.
  • 同义词
    MLN 8237 | MLN8237 | MLN-8237
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    Aurora Kinase
  • 受体
    AuroraA|AuroraB
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    1028486-01-2
  • 分子量
    518.9235
  • 分子式
    C27H20ClFN4O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 9.33 mg/mL
  • SMILES
    O=C(O)C1=CC=C(NC2=NC=C3C(C4=CC=C(Cl)C=C4C(C5=C(OC)C=CC=C5F)=NC3)=N2)C=C1OC
  • 化学全称
    Benzoic acid, 4-[[9-chloro-7-(2-fluoro-6-methoxyphenyl)-5H-pyrimido[5,4-d][2]benzazepin-2-yl]amino]-2-methoxy-

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. Manfredi MG, et al. Clin Cancer Res. 2011 Dec 15;17(24):7614-24. 2. Wen Q, et al. Cell. 2012 Aug 3;150(3):575-89. 3. Zhou N, et al. Clin Cancer Res. 2013 Apr 1;19(7):1717-28.
产品手册
关联产品
  • BPR1K653

    BPR1K653 是一种新型强效 Aurora 激酶抑制剂,可抑制 Aurora-A 和 Aurora-B,IC50 分别为 24 nM 和 45 nM。

  • Aurora A-IN-10

    一种有效的、高选择性的 Aurora A 抑制剂,IC50 为 3.4 nM;与 Aurora B (IC50=3.4 uM) 或 CDK 相比,显示出 >1,000 倍的选择性。

  • LY3295668

    LY3295668 (LY-3295668, AK-01) 是一种新型强效、高选择性、口服活性的 Aurora-A 激酶抑制剂,Ki 为 0.8 nM,H446 AurA auto-P IC50 为 0.6 nM。