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BC-DXI-843

CAS No. 2421117-98-6

BC-DXI-843 ( —— )

产品货号. M22007 CAS No. 2421117-98-6

BC-DXI-843 是 AIMP2-DX2 的抑制剂,具有开发针对肺癌的 AIMP2-DX2 新型疗法的潜力。

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 是 AIMP2-DX2 的抑制剂,具有开发针对肺癌的 AIMP2-DX2 新型疗法的潜力。
  • 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.
  • 体外实验
    BC-DXI-843 (0.0316-31.6 μM; 72 hours) suppresses cancer cell proliferation in a DX2-dependent manner. The EC50 in A549 cells is 1.20 μM, which is similar to the IC50 for inhibition of DX2. However, no inhibition of WI-26 cells is observed, suggesting that BC-DXI-843 specifically reduces the viability of cancer cells. Cell Proliferation Assay Cell Line:A549 cancer cells and WI-26 normal cells Concentration:0.0316, 0.1, 0.316, 1, 3.16, 10, 31.6 μM Incubation Time:72 hours Result:The EC50 in A549 cells was 1.20 μM. No inhibition of WI-26 cells was observed.
  • 体内实验
    BC-DXI-843 (50 mg/kg; intraperitoneally administered; every other day for 15 days) demonstrates in vivo efficacy in a tumor xenograft mouse model (H460 cells). Animal Model:7-week-old female BALB/cSLC-nu/nu mice bearing H460 cells xenograft Dosage:50 mg/kg Administration:Intraperitoneally administered; every other day for 15 days Result:The embedded tumor volume gradually declined after BC-DXI-843administration, but no changes in body weight were observed. The weight of the excised tumors after sacrifice had decreased in mice.
  • 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.
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