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AT-7519 hydrochloride

CAS No. 902135-91-5

AT-7519 hydrochloride ( AT 7519 Hydrochloride | AT7519 Hydrochloride )

产品货号. M16486 CAS No. 902135-91-5

一种有效的 CDK2 抑制剂,IC50 为 47 nM;还抑制 CDK1/4/5,IC50 为 190/67/18 nM,并对某些激酶(Aurora A、IR 激酶、MEK、PDK1、c-Abl,IC50>10 uM)表现出选择性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥392 有现货
10MG ¥629 有现货
25MG ¥1228 有现货
50MG ¥1972 有现货
100MG ¥3042 有现货
500MG ¥6836 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥432 有现货

生物学信息

  • 产品名称
    AT-7519 hydrochloride
  • 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
    一种有效的 CDK2 抑制剂,IC50 为 47 nM;还抑制 CDK1/4/5,IC50 为 190/67/18 nM,并对某些激酶(Aurora A、IR 激酶、MEK、PDK1、c-Abl,IC50>10 uM)表现出选择性。
  • 产品描述
    A potent CDK2 inhibitor with IC50 of 47 nM; also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM); has antiproliferative activity against HCT116 cells with IC50 of 82 nM; exhibits good profile against cytochrome P450 isoforms (<30% inhibition at 10 uM for 1A2, 2D6, 3A4, 2C9, 2C19).Blood Cancer Phase 2 Clinical(In Vitro):AT7519 (0-4 μM) results in dose-dependent cytotoxicity with IC50s ranging from 0.5 to 2 μM in MM cells, and this induced cytotoxicity is associated with GSK-3β activation independent of transcriptional inhibition. AT7519 overcomes proliferative advantage conferred by cytokines and the protective effect of BMSC. AT7519 (0.5 μM) induces apoptosis of MM cells in a time-dependent manner. Moreover, AT7519 (0.5 μM) inhibits phosphorylation of RNA polymerase II CTD and partially inhibits RNA synthesis in MM.1S cells. AT7519 (250 nM) inhibits cell cycle progression in human tumor cell lines. AT7519 also induces apoptosis of human tumor cell lines. AT7519 (100-700 nM) induces apoptosis in leukemia cell lines. AT7519 also inhibits transcription in human tumor cell lines. Furthermore, AT7519 inhibits RNA polymerase II and reduces antiapoptotic protein levels.(In Vivo):AT7519 inhibits tumor growth in a human MM xenograft mouse model. AT7519 (4.6 and 9.1 mg/kg/dose) inhibits the growth of early-stage HCT116 tumor xenografts. AT7519 (10 mg/kg, i.p.) also inhibits the target CDKs in HCT116 tumor-bearing BALB/c nude mice.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    AT 7519 Hydrochloride | AT7519 Hydrochloride
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    CDK
  • 受体
    CDK2/CyclinA|CDK4/CyclinD1|CDK5/p35|CDK9/CyclinT|GSK-3β
  • 研究领域
    Cancer
  • 适应症
    Blood cancer

化学信息

  • CAS Number
    902135-91-5
  • 分子量
    418.7054
  • 分子式
    C16H18Cl3N5O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    10 mM in DMSO
  • SMILES
    Cl.CC1=C(C(=O)NC2=C(NN=C2)C(=O)NC2CCNCC2)C(Cl)=CC=C1
  • 化学全称
    1H-Pyrazole-3-carboxamide, 4-[(2,6-dichlorobenzoyl)amino]-N-4-piperidinyl-, hydrochloride (1:1)

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. Wyatt PG, et al. J Med Chem. 2008 Aug 28;51(16):4986-99. 2. Squires MS, et al. Mol Cancer Ther. 2009 Feb;8(2):324-32. 3. Dolman ME, et al. Clin Cancer Res. 2015 Nov 15;21(22):5100-9.
产品手册
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