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 |
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10MG | ¥583 | 有现货 |
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25MG | ¥1045 | 有现货 |
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50MG | ¥1725 | 有现货 |
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100MG | ¥2608 | 有现货 |
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200MG | ¥3872 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称KIN101
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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
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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。
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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.
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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.
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体内实验——
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同义词3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene
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通路Microbiology/Virology
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靶点HCV
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受体NMDA
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研究领域——
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适应症——
化学信息
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CAS Number610753-87-2
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分子量395.22
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分子式C16H11BrO5S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 41.67 mg/mL (105.43 mM)
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SMILESCS(=O)(=O)Oc1ccc2c(c1)occ(-c1ccc(Br)cc1)c2=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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