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JNJ-7706621

Cat. No.:YN270052

  • CAS No. :443797-96-4

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    • 产品名称: JNJ-7706621
      CAS No.: 443797-96-4
      Chemical Name: 4-[[5-amino-1-(2,6-difluorobenzoyl)-1H-1,2,4-triazol-3-yl]amino]-benzenesulfonamide
      Synonyms:JNJ 7706621
      分子量:394.36
      分子式:C₁₅H₁₂F₂N₆O₃S
      SMILES:O=S(C1=CC=C(NC2=NN(C(C3=C(F)C=CC=C3F)=O)C(N)=N2)C=C1)(N)=O
      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: JNJ-7706621 是一种有效的aurora kinase抑制剂,同时能有效抑制CDK1和CDK2,对CDK1,CDK2,aurora-A和aurora-B的IC50值分别为 9 nM,3 nM,11 nM 和 15 nM。
      IC50和靶点: [{name:"CDK6/cyclinD1:175 nM (IC50)"},{name: "CDK2/cyclinE:3 nM (IC50)"},{name: "Cdk4/cyclin D1:253 nM (IC50)"},{name: "Cdk1/cyclin B:9 nM (IC50)"},{name: "cdk2/cyclin A:4 nM (IC50)"},{name: "CDK3/Cyclin E:58 nM (IC50)"},{name: "Aurora A:11 nM (IC50)"},{name: "Aurora B:15 nM (IC50)"},{name: "VEGF-R2:154 nM (IC50)"},{name: "VEGF-R1:6400 nM (IC50)"},{name: "VEGF-R3:735 nM (IC50)"},{name: "FGF-R1:575 nM (IC50)"},{name: "FGF-R2:226 nM (IC50)"},{name: "GSK3β:254 nM (IC50)"}]
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Emanuel, S., Rugg, C.A., Gruninger, R.H., et al.The in vitro and in vivo effects of JNJ-7706621: a dual inhibitor of cyclin-dependent kinases and aurora kinasesCancer Res.65(19),9038-9046(2005)

      Seamon, J.A., Rugg, C.A., Emanuel, S., et al.Role of the ABCG2 drug transporter in the resistance and oral bioavailability of a potent cyclin-dependent kinase/Aurora kinase inhibitorMol. Cancer Ther.5(10),2459-2467(2006)

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