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BMY-27709

BMY-27709

产品编号 T26873   CAS 99390-76-8
别名: BMY 27709, BMY27709

BMY-27709 是一种流感病毒生长抑制剂,对 A/WSN/33 病毒生长的 IC50 值为 3-8 μM,对流感病毒的部分亚型也展现出抑制活性。BMY-27709 对 H1 和 H2 病毒感染的早期起作用,通过抑制血凝素蛋白展现其抗病毒活性。然而,BMY-27709 对 H3 亚型病毒以及 B 型/Lee/40 流感病毒没有作用。

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BMY-27709 Chemical Structure
BMY-27709, CAS 99390-76-8
规格 价格/CNY 货期 数量
1 mg ¥ 2,350 现货
5 mg ¥ 5,630 现货
10 mg ¥ 7,790 现货
25 mg ¥ 11,200 现货
50 mg ¥ 13,800 现货
100 mg ¥ 17,500 现货
500 mg ¥ 34,800 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
Doxorubicin hydrochloride限时半价
产品目录号及名称: BMY-27709 (T26873)
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纯度: 100%
纯度: 98.07%
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生物活性
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参考文献
产品描述 BMY-27709 is an influenza virus growth inhibitor with an IC50 value of 3-8 μM against A/WSN/33 virus growth, and also exhibits inhibitory activity against some subtypes of influenza viruses.BMY-27709 acts early in the course of H1 and H2 virus infections, and exhibits antiviral activity through inhibition of hemagglutinin proteins. However, BMY-27709 has no effect on H3 subtype viruses and influenza B/Lee/40 viruses.
体外活性 BMY-27709 has an IC50 of 3-8 microM for a WSN 33 virus growth in a multicycle replication assay and is active against all H1 and H2 subtype viruses tested. However, BMY-27709 was found to be inactive against H3 subtype viruses, as well as influenza B/Lee/40 virus. BMY-27709 was also found to act against H1 and H2 viruses early in infection, suggesting that the target for inhibition is the hemagglutinin protein. This was confirmed through the use of reassortant viruses and the isolation of a virus resistant to BMY-27709. The resistant virus isolated contained phenylalanine to serine change at amino acid 110 of the HA2 subunit. That this single mutation was responsible for the acquisition of resistance to BMY-27709 was proven through reverse genetics, as a transfectant virus containing only this change was shown to be resistant to BMY-27709, while the control virus without this mutation remained sensitive. BMY-27709 is able to inhibit virus-induced red blood cell hemolysis, suggesting that it blocks the membrane fusion function of hemagglutinin. These experiments further illustrate that the hemagglutinin protein of the influenza virus is a viable target for the discovery and development of small-molecule inhibitors of virus growth.[1]
别名 BMY 27709, BMY27709
分子量 337.84
分子式 C17H24ClN3O2
CAS No. 99390-76-8

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

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TargetMol Library Books参考文献

1. Luo G, et al. Characterization of a hemagglutinin-specific inhibitor of influenza A virus. Virology. 1996;226(1):66-76. 2. Luo G, et al. Molecular mechanism underlying the action of a novel fusion inhibitor of influenza A virus. J Virol. 1997;71(5):4062-4070. 3. Combrink KD, et al. Salicylamide inhibitors of influenza virus fusion. Bioorg Med Chem Lett. 2000;10(15):1649-1652. 4. Hsieh HP, et al. Strategies of development of antiviral agents directed against influenza virus replication. Curr Pharm Des. 2007;13(34):3531-3542.
Arctigenin β-Cyclodextrin Laninamivir Ginsenoside Rb2 7-51A Sophocarpine monohydrate Dihydromyricetin Dehydroandrographolide succinate

相关化合物库

该产品包含在如下化合物库中:
抑制剂库 抗病毒库 经典已知活性库 已知活性化合物库

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您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

BMY-27709 99390-76-8 Microbiology/Virology Influenza Virus BMY 27709 BMY27709 Inhibitor inhibitor inhibit

 

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