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KIN101
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
KIN101图片
规格:98%
分子量:395.22
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
KIN101 是有效的 RNA 病毒 (RNA viral) 抑制剂,对流感病毒 (influenza virus) 和登革热病毒 (DNV) 的 IC50 分别为 2 μM,>5 μM。KIN101 是一种 IRF-3 依赖性信号传导的异黄酮激动剂,可以诱导 IRF-3 核易位。KIN101 具有针对 RNA 病毒的广谱活性。
货号:ajcx37254
CAS:610753-87-2
分子式:C16H11BrO5S
分子量:395.22
溶解度:DMSO : 41.67 mg/mL (105.43 mM; ultrasonic and warming and heat to 60°C)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

KIN101 is a potent RNA viral inhibitor with IC50s of 2 μM, >5 μM for influenza virus and Dengue virus (DNV), respectively. KIN101, an isoflavone agonist of IRF-3 dependent signaling, induces IRF-3 nuclear translocation. KIN101 has broad-spectrum activity against RNA viruses[1][2].

KIN 101 (10 μM; 24 hours) causes a significant decrease in the NP protein abundance[1].KIN 101 (10 μM; 18 hours) shows a >1 log decrease in HCV RNA levels[1].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[1].KIN 101 (5, 10, 20, 50 μM; 4 hours) causes a dose-dependent decrease in influenza virus infection in MRC5 cells[1].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[1].KIN101 (0.1-100 μM; 18 hours) shows the antiviral activity against hepatitis C virus (HCV)[2].

[1]. Bedard KM, et al. Isoflavone agonists of IRF-3 dependent signaling have antiviral activity against RNA viruses. J Virol. 2012 Jul;86(13):7334-44.
[2]. Shawn P. Iadonato, et al. Anti-viral compounds, pharmaceutical compositions and methods of use thereof. US20160122312A1.