• 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

Bohemine

CAS No. 189232-42-6

Bohemine ( Bohemine )

产品货号. M12967 CAS No. 189232-42-6

Bohemine 是一种细胞周期蛋白依赖性激酶抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥381 有现货
10MG ¥583 有现货
25MG ¥1077 有现货
50MG ¥1936 有现货
100MG ¥3013 有现货
200MG ¥4447 有现货
500MG ¥7039 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Bohemine
  • 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
    Bohemine 是一种细胞周期蛋白依赖性激酶抑制剂。
  • 产品描述
    Bohemine is a cyclin-dependent kinase inhibitor.
  • 体外实验
    Bohemine (0-30 μM; 72 hours; ME-750 cells) treatment inhibits cell growth. Addition of Bohemine at concentrations in the range of 1-10 μM results in a short-term arrest of growth and of monoclonal antibody production. The short-term suppression of cell functions is followed by a significant temporary increase of specific growth rate and of specific production rate.Hybridoma cells are retarded both at the G1/S boundary and at the G2/M boundary, depending on Bohemine (0-30 μM) concentration.T-lymphoblastic cell line CEM is treated by Bohemine, five proteins are found to be downregulated, namely α-enolase, triosephosphate isomerase, initiation factor 5A, and α- and β-subunits of Rho GDP-dissociation inhibitor 1. These proteins play significant roles in glycolysis, proteosynthesis, and in cytoskeleton rearrangement.Bohemine inhibits growth of human tumor cell lines with an IC50 of 27 μM. Cell Viability Assay Cell Line:Mouse hybridoma ME-750 cells Concentration:0 μM, 1 μM, 3 μM, 10 μM and 30 μM Incubation Time:72 hours Result:At 10 μM and 30 μM concentrations, the viable cell count was significantly lower with respect to control, i.e., 77% and 48%, respectively.
  • 体内实验
    Bohemine (50 mg/kg; intravenous injection; BALB/c mice) treatment shows Cmax is 72,308 nM, observed clearance is 0.23 L/h and T1/2 is 1.39 h. Animal Model:BALB/c mice bearing the colon 26 murine tumorDosage:50 mg/kg Administration:Intravenous injection (Pharmacokinetic Analysis) Result:Cmax is 72,308 nM, observed clearance is 0.23 L/h and T1/2 is 1.39 h.
  • 同义词
    Bohemine
  • 通路
    Angiogenesis
  • 靶点
    CDK
  • 受体
    CDK
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    189232-42-6
  • 分子量
    340.42
  • 分子式
    C18H24N6O
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 10 mM
  • SMILES
    CC(N1C=NC2=C1N=C(NCCCO)N=C2NCC3=CC=CC=C3)C
  • 化学全称
    3-((6-(benzylamino)-9-isopropyl-9H-purin-2-yl)amino)propan-1-ol

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.Liskova B, et al. Chem Res Toxicol. 2012 Feb 20;25(2):500-9.
产品手册
关联产品
  • NSC 625987

    NSC 625987 是一种有效的选择性 CDK4 抑制剂,IC50 为 0.2 uM,选择性比 CDK2 高 500 倍(cdc2/cyclin A、cdk2/cyclin A 和 cdk2/cyclin E 的 IC50 >100 uM)。

  • Senexin B

    Senexin B (SNX2-1-165) 是一种高效、选择性、口服的 CDK8/CDK19 抑制剂,IC50 为 24-50 nM。

  • SU-9516

    一种选择性 CDK2 抑制剂,IC50 为 22 nM;对 CDK1/CDK4 的抑制作用较弱(IC50=40/200 nM),对 PKC、EGFR、p38MAPK 无抑制作用;降低 pRb 的磷酸化,并增加 caspase-3 的激活。