• 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

BC-DXI-843

CAS No. 2421117-98-6

BC-DXI-843 ( —— )

产品货号. M22007 CAS No. 2421117-98-6

BC-DXI-843 is inhibitor of AIMP2-DX2, and is potential for development of novel therapeutics targeting AIMP2-DX2 in lung cancer.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥478 有现货
5MG ¥753 有现货
10MG ¥1256 有现货
25MG ¥2333 有现货
50MG ¥3507 有现货
100MG ¥5144 有现货
200MG 获取报价 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
    BC-DXI-843
  • 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
    BC-DXI-843 is inhibitor of AIMP2-DX2, and is potential for development of novel therapeutics targeting AIMP2-DX2 in lung cancer.
  • 产品描述
    BC-DXI-843 is inhibitor of AIMP2-DX2, and is potential for development of novel therapeutics targeting AIMP2-DX2 in lung cancer.Optimization of hit BC-DXI-04 (IC50 = 40.1 μM) provided new potent sulfonamide based AIMP2-DX2 inhibitors.?Among these, BC-DXI-843 showed improved inhibition against AIMP2-DX2 (IC50 = 0.92 μM) with more than 100-fold selectivity over AIMP2 in a luciferase assay.?Several binding assays indicated that this compound effectively induces cancer cell apoptosis by specifically interrupting the interaction between DX2 and HSP70, which leads to the degradation of DX2 via Siah1-mediated ubiquitination.BC-DXI-843 demonstrated in vivo efficacy in a tumor xenograft mouse model (H460 cells) at a dosage of 50 mg/kg, suggesting it as a promising lead for development of novel therapeutics targeting AIMP2-DX2 in lung cancer.
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    AIMP2-DX2
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2421117-98-6
  • 分子量
    546.66
  • 分子式
    C28H26N4O4S2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:245mg/ml (448.18 Mm; Need ultrasonic)
  • SMILES
    COC1=CC=C(C=C1)C1=CSC(NC(=O)[C@H](CC2=CNC3=CC=CC=C23)NS(=O)(=O)C2=CC=C(C)C=C2)=N1
  • 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.Aneesh Sivaraman, Dae Gyu Kim, Deepak Bhattarai,et al. Synthesis and Structure-Activity Relationships of Arylsulfonamides as AIMP2-DX2 Inhibitors for the Development of a Novel Anticancer Therapy. J Med Chem. 2020 May 28;63(10):5139-5158.
产品手册
关联产品
  • Curzerenone

    Curzerenone holds great promise for use in chemopreventive and chemotherapeutic strategies, it has slightly effective against E. coli (IZ = 10.8 ± 0.52).

  • Amino-PEG13-amine

    Amino-PEG13-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

  • Isolindleyin

    Isolindleyin is a natural product.