• 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

Batabulin

CAS No. 195533-53-0

Batabulin ( T138067 )

产品货号. M23886 CAS No. 195533-53-0

Batabulin is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥988 有现货
10MG ¥1442 有现货
25MG ¥2535 有现货
50MG ¥3750 有现货
100MG ¥5411 有现货
500MG ¥11178 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Batabulin
  • 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
    Batabulin is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization.
  • 产品描述
    Batabulin is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization. Batabulin affects cell morphology and leads to cell-cycle arrest ultimately induce apoptotic cell death.
  • 同义词
    T138067
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    Apoptosis;Tubulin β
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    195533-53-0
  • 分子量
    371.3
  • 分子式
    C13H7F6NO3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:100 mg/mL (269.35 mM; Need ultrasonic)
  • SMILES
    O=S(C1=C(F)C(F)=C(F)C(F)=C1F)(NC2=CC=C(OC)C(F)=C2)=O
  • 化学全称
    ——

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.Shan B, et al. Selective, covalent modification of beta-tubulin residue Cys-239 by T138067, an antitumor agent with in vivo efficacy against multidrug-resistant tumors. Proc Natl Acad Sci U S A. 1999 May 11;96(10):5686-91.
产品手册
关联产品
  • physalin F

    Physalin F is a natural blocker of CaV2.3 (R-type) and CaV2.2 (N-type) voltage-gated calcium channels.It is a secosteroid with potent anti-inflammatory and immunomodulatory activities.

  • Talampanel

    Talampanel is an orally and selective α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptor antagonist with anti-seizure activity.

  • CHM-1

    CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.