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BAY-876

Cat. No.:YN360003

  • CAS No. :1799753-84-6

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    • 生物活性
    • 参考文献
    • 产品名称: BAY-876
      CAS No.: 1799753-84-6
      Chemical Name: N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-2,4-quinolinedicarboxamide
      Synonyms:BAY-876;BAY876;N4-[1-[(4-Cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-2,4-quinolinedicarboxamide;BAY 876;N4-(1-(4-Cyanobenzyl)-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)-7-fluoroquinoline-2,4-dicarboxamide;BCP25065;s8452;S
      分子量:496.42
      分子式:C₂₄H₁₆F₄N₆O₂
      SMILES:O=C(C1=NC2=CC(F)=CC=C2C(C(NC3=C(C)N(CC4=CC=C(C#N)C=C4)N=C3C(F)(F)F)=O)=C1)N
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: BAY-876 是一种具有口服活性的,选择性的葡萄糖转运蛋白 1 (GLUT1) 抑制剂,IC50为 2 nM。BAY-876 对GLUT1的选择性是 GLUT2,GLUT3 和 GLUT4 的 130 倍以上。BAY-876 还是一种糖酵解代谢和卵巢癌生长的有效阻滞剂。
      IC50和靶点: [{name:"GLUT1:2 nM (IC50)"},{name: "GLUT2:10.08 μM (IC50)"},{name: "GLUT3:1.67 μM (IC50)"},{name: "GLUT4:0.29 μM (IC50)"}]
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Siebeneicher, H., Cleve, A., Rehwinkel, H., et al.Identification and optimization of the first highly selective GLUT1 inhibitor BAY-876ChemMedChem11(20),2261-2271(2016)

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