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Influenza virus

Products for  Influenza virus

  1. Cat.No. Product Name Information
  2. GC63814 Amantadine Amantadine (1-Adamantanamine) is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine  Chemical Structure
  3. GC70262 Amitivir Amitivir (LY 217896), a thiadiazole derivative, possesses broad antiviral activity against orthomyxo- and paramyxoviruses. Amitivir  Chemical Structure
  4. GC72208 Asp-Asp-Asp-Asp-Asp-Asp Asp-Asp-Asp-Asp-Asp-Asp is a polyaspartic acid. Asp-Asp-Asp-Asp-Asp-Asp  Chemical Structure
  5. GC71694 Chloroxylenol-d6 Chloroxylenol-d6 is the deuterium labeled Chloroxylenol. Chloroxylenol-d6  Chemical Structure
  6. GC68881 Clemastanin B

    Clemastanin B is a lignin that has strong anti-influenza activity by inhibiting virus proliferation, preventing and blocking virus attachment. Clemastanin B targets the internalization of viruses, uncoating or ribonucleoprotein (RNP) export from the cell nucleus. It also has antioxidant and anti-inflammatory activities.

    Clemastanin B  Chemical Structure
  7. GC64348 Cyanidin 3-sambubioside chloride Cyanidin 3-sambubioside chloride (Cyanidin-3-O-sambubioside chloride), a major anthocyanin, a natural colorant, and is a potent NO inhibitor. Cyanidin 3-sambubioside chloride  Chemical Structure
  8. GC72450 Diridavumab Diridavumab is a monoclonal anti-HA stalk antibody. Diridavumab  Chemical Structure
  9. GC63987 Eleutheroside B1

    Eleutheroside B1, a coumarin compound, has a wide spectrum of anti-human influenza virus efficacy, with an IC50 value of 64-125μg/ml.

    Eleutheroside B1  Chemical Structure
  10. GC72414 Firivumab Firivumab (CT-P22; CT120) is a human IgG1 monoclonal influenza A virus hemagglutinin (Anti-IAV HA) antibody. Firivumab  Chemical Structure
  11. GC65043 Haemanthamine Haemanthamine is a crinine-type alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. Haemanthamine  Chemical Structure
  12. GC70644 Influenza A virus-IN-1 Influenza A virus-IN-1 is a dihydropyrrolidones derivative and is a potent inhibitor against wide subtypes of influenza A virus (IAV) with IC50 values from 3.11 μM to 7.13 μM. Influenza A virus-IN-1  Chemical Structure
  13. GC65968 JNJ4796 JNJ4796 is an oral active fusion inhibitor of influenza virus, neutralizing influenza A group 1 viruses by inhibiting hemagglutinin (HA)-mediated fusion. JNJ4796 mimics the functionality of the broadly neutralizing antibodies (bnAbs). JNJ4796  Chemical Structure
  14. GC64253 KIN101 KIN101 is a potent RNA viral inhibitor with IC50s of 2 μM, >5 μM for influenza virus and Dengue virus (DNV), respectively. KIN101  Chemical Structure
  15. GC65069 Laninamivir Laninamivir (R 125489) is a potent influenza neuraminidase (NA) inhibitor with IC50s of 0.90 nM, 1.83 nM and 3.12 nM for avian H12N5 NA (N5), pH1N1 N1 NA (p09N1) and A/RI/5+/1957 H2N2 N2 (p57N2), respectively. Laninamivir  Chemical Structure
  16. GC64228 MBX2329 MBX2329, a potent influenza virus inhibitor, specifically inhibits hemagglutinin (HA)-mediated viral entry with HIV/HA(H5) displaying IC90 of 8.6 μM. MBX2329  Chemical Structure
  17. GC65122 ML303 ML303 is a pyrazolopyridine influenza virus nonstructural protein 1 (NS1) antagonist (IC90 = 155 nM), with an EC50 of 0.7 μM for Influenza A virus H1N1. ML303  Chemical Structure
  18. GC72432 Navivumab Navivumab (CT-P23) is an influenza A virus hemagglutinin HA monoclonal antibody. neutralizes H1, H2, H5, and H9 influenza A viruses by binding to the stem fusion domain in HA2. Navivumab  Chemical Structure
  19. GC70932 Onradivir Onradivir is a potent anti-influenza virus agent. Onradivir  Chemical Structure
  20. GC64333 Oseltamivir-d5 phosphate

    GS 4104-d5

    Oseltamivir-d5 phosphate  Chemical Structure
  21. GC64254 Rifampicin-d4

    Rifampin-d4; Rifamycin AMP-d4

    Rifampicin-d4  Chemical Structure
  22. GC63911 Rifampicin-d8 Rifampicin-d8  Chemical Structure
  23. GC68428 Rimantadine-d4 hydrochloride Rimantadine-d4 hydrochloride  Chemical Structure
  24. GC64223 Sophocarpine monohydrate Sophocarpine (monohydrate) is one of the significant alkaloid extracted from the traditional herb medicine Sophora flavescens which has many pharmacological properties such as anti-virus, anti-tumor, anti-inflammatory. Sophocarpine monohydrate  Chemical Structure
  25. GC71370 Trifluoromethyl-tubercidin Trifluoromethyl-tubercidin (TFMT) is a 2'-O-ribose methyltransferase 1 (MTr1) inhibitor through interaction at its S-adenosyl-l-methionine binding pocket to restrict influenza virus replication. Trifluoromethyl-tubercidin  Chemical Structure

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