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KIN101

CAS No. 610753-87-2

KIN101 ( 3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene )

产品货号. M26270 CAS No. 610753-87-2

KIN101 是 IRF-3 依赖性信号传导的异黄酮激动剂,可诱导 IRF-3 核转位。 KIN101 对 RNA 病毒、HCV 和 RSV 具有抗病毒活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥381 有现货
10MG ¥583 有现货
25MG ¥1045 有现货
50MG ¥1725 有现货
100MG ¥2608 有现货
200MG ¥3872 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
    KIN101
  • 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
    KIN101 是 IRF-3 依赖性信号传导的异黄酮激动剂,可诱导 IRF-3 核转位。 KIN101 对 RNA 病毒、HCV 和 RSV 具有抗病毒活性。
  • 产品描述
    KIN101, an isoflavone agonist of IRF-3 dependent signaling, induces IRF-3 nuclear translocation. KIN101 has antiviral activity against RNA viruses, HCV, and RSV.(In Vitro):KIN101 results in a significant increase in the levels of ISGs as well as other proteins downstream of IRF activation such as RIG-I and MDA5.KIN101 (10 μM; 24 hours) causes a significant decrease in the NP protein abundance. KIN 101 (10 μM; 18 hours) shows a >1 log decrease in HCV RNA levels. KIN 101 (5, 10, 20, 50 μM; 4 hours) causes a dose-dependent decrease in influenza virus infection in MRC5 cells. KIN101 (0.01, 0.1, 1, 10, 100 μM) has a significant and dose-dependent effect on the formation of foci and has an IC50 of 0.2 μM.
  • 体外实验
    KIN 101 (10 μM; 24 hours) causes a significant decrease in the NP protein abundance.KIN 101 (10 μM; 18 hours) shows a >1 log decrease in HCV RNA levels.KIN 101 (0.01, 0.1, 1, 10, 100 μM) has a significant and dose-dependent effect on the formation of foci and has an IC50 of 0.2 μM.KIN 101 (5, 10, 20, 50 μM; 4 hours) causes a dose-dependent decrease in influenza virus infection in MRC5 cells.KIN 101 results in a significant increase in the levels of ISGs as well as other proteins downstream of IRF activation such as RIG-I and MDA5.KIN101 (0.1-100 μM; 18 hours) shows the antiviral activity against hepatitis C virus (HCV). Western Blot Analysis Cell Line:MRC5 cells Concentration:10 μM Incubation Time:24 hours Result:Caused a significant decrease in the NP protein abundance. RT-PCR Cell Line:Huh7 cells Concentration:10 μM Incubation Time:18 hours Result:Showed a >1 log decrease in HCV RNA levels.
  • 体内实验
    ——
  • 同义词
    3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene
  • 通路
    Microbiology/Virology
  • 靶点
    HCV
  • 受体
    NMDA
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    610753-87-2
  • 分子量
    395.22
  • 分子式
    C16H11BrO5S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 41.67 mg/mL (105.43 mM)
  • SMILES
    CS(=O)(=O)Oc1ccc2c(c1)occ(-c1ccc(Br)cc1)c2=O
  • 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.Parsons CG, et al. Novel systemically active antagonists of the glycine site of the N-methyl-D-aspartate receptor: electrophysiological, biochemical and behavioral characterization. Journal of Pharmacology and Experimental Therapeutics (1997), 283(3), 1264-1275
产品手册
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