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Tegobuvir

CAS No. 1000787-75-6

Tegobuvir ( GS 333126 | GS 9190 | GS333126 | GS9190 )

产品货号. M10009 CAS No. 1000787-75-6

HCV NS5B 聚合酶的非核苷抑制剂,可作为 HCV 基因型 1 的有效抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1968 有现货
10MG ¥3345 有现货
25MG ¥5573 有现货
50MG ¥7930 有现货
100MG ¥10692 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
    Tegobuvir
  • 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
    HCV NS5B 聚合酶的非核苷抑制剂,可作为 HCV 基因型 1 的有效抑制剂。
  • 产品描述
    A nonnucleoside inhibitor of HCV NS5B polymerase that acts as a potent inhibitor of HCV genotype 1; inhibits 1a (H77) and 1b (Con-1) replicons with EC50 of 13.8 nM and 0.8 nM respectively, and displays a loss in potency against 2a (JFH-1) virus with EC50 of 2.9 uM.(In Vitro):Tegobuvir rapidly increases the proportion of replicons with the Y448H mutation in a dose-dependent manner. After 3 days of treatment, 1.2%, 6.8%, and > 50% of the replicon population expresses Y448H with the use of Tegobuvir at 1, 10, and 20 times its 50% effective concentration, respectively. Tegobuvir exerts anti-HCV activity utilizing a unique chemical activation and subsequent direct interaction with the NS5B protein. Treatment of HCV subgenomic replicon cells with Tegobuvir results in a modified form of NS5B with a distinctly altered mobility on a SDS-PAGE gel. Tegobuvir is potent in GT1a and 1b with mean EC50s of 19.8 and 1.5 nM respectively. For genotype 3a, 4a, and 6a Con chimeras, tegobuvir EC50s are all greater than 100 nM. The F445C NS5B mutations in GT3a, 4a, and 6a chimeric replicons restore tegobuvir potency to EC50 levels comparable to GT1a.
  • 体外实验
    Tegobuvir rapidly increases the proportion of replicons with the Y448H mutation in a dose-dependent manner. After 3 days of treatment, 1.2%, 6.8%, and > 50% of the replicon population expresses Y448H with the use of Tegobuvir at 1, 10, and 20 times its 50% effective concentration, respectively. Tegobuvir exerts anti-HCV activity utilizing a unique chemical activation and subsequent direct interaction with the NS5B protein. Treatment of HCV subgenomic replicon cells with Tegobuvir results in a modified form of NS5B with a distinctly altered mobility on a SDS-PAGE gel. Tegobuvir is potent in GT1a and 1b with mean EC50s of 19.8 and 1.5 nM respectively. For genotype 3a, 4a, and 6a Con chimeras, tegobuvir EC50s are all greater than 100 nM. The F445C NS5B mutations in GT3a, 4a, and 6a chimeric replicons restore tegobuvir potency to EC50 levels comparable to GT1a.
  • 体内实验
    ——
  • 同义词
    GS 333126 | GS 9190 | GS333126 | GS9190
  • 通路
    Microbiology/Virology
  • 靶点
    HCV
  • 受体
    HCV
  • 研究领域
    Infection
  • 适应症
    ——

化学信息

  • CAS Number
    1000787-75-6
  • 分子量
    517.401
  • 分子式
    C25H14F7N5
  • 纯度
    >98% (HPLC)
  • 溶解度
    10 mM in DMSO
  • SMILES
    FC1=CC=CC=C1C2=NC3=CN(CC4=NN=C(C5=CC=C(C(F)(F)F)C=C5C(F)(F)F)C=C4)C=CC3=N2
  • 化学全称
    5H-Imidazo[4,5-c]pyridine, 5-[[6-[2,4-bis(trifluoromethyl)phenyl]-3-pyridazinyl]methyl]-2-(2-fluorophenyl)-

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. Shih IH, et al. Antimicrob Agents Chemother. 2011 Sep;55(9):4196-203. 2. Zeuzem S, et al. Hepatology. 2012 Mar;55(3):749-58. 3. Wong KA, et al. Virology. 2012 Jul 20;429(1):57-62.
产品手册
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