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 |
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5MG | ¥753 | 有现货 |
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10MG | ¥1256 | 有现货 |
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25MG | ¥2333 | 有现货 |
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50MG | ¥3507 | 有现货 |
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100MG | ¥5144 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称BC-DXI-843
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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
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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.
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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.
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同义词——
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通路Others
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靶点Other Targets
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受体AIMP2-DX2
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研究领域——
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适应症——
化学信息
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CAS Number2421117-98-6
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分子量546.66
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分子式C28H26N4O4S2
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纯度>98% (HPLC)
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溶解度DMSO:245mg/ml (448.18 Mm; Need ultrasonic)
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SMILESCOC1=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
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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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