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Vírus da Influenza

Vírus da Influenza

Os inibidores do vírus da gripe são compostos que interferem na replicação e disseminação dos vírus da gripe. Esses inibidores são essenciais para pesquisar estratégias antivirais, compreender o ciclo de vida do vírus da gripe e desenvolver tratamentos e vacinas eficazes. Os inibidores da gripe podem atuar em várias etapas do processo de replicação viral, incluindo a entrada viral, replicação e liberação. Na CymitQuimica, oferecemos uma ampla gama de inibidores de alta qualidade do vírus da gripe para apoiar sua pesquisa em virologia, doenças infecciosas e desenvolvimento de medicamentos antivirais.

Foram encontrados 301 produtos de "Vírus da Influenza"

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  • Cap-dependent endonuclease-IN-17

    CAS:
    CEN inhibitor IN-17 targets influenza A/H3N2; IC50: 1.29 μM. From patent CN112898346A, DSC701.
    Fórmula:C24H20F2N3O7PS
    Cor e Forma:Solid
    Peso molecular:563.47
  • UNC0638 hydrate

    CAS:
    UNC0638 hydrate selectively inhibits G9a and GLP histone methyltransferases with IC50 values of 15 nM and 19 nM, respectively. It is effective in inhibiting invasion and migration of TNBC cells in vitro. Additionally, UNC0638 hydrate acts as an inhibitor of EHMT1/2 and induces the expression of fetal hemoglobin (HbF) in cultures of human erythroid progenitor cells. Furthermore, it exhibits antiviral activity against FMDV (foot-and-mouth disease virus) and VSV (vesicular stomatitis virus), demonstrating remarkable potency and selectivity across various epigenetic and non-epigenetic targets.
    Fórmula:C30H49N5O3
    Cor e Forma:Solid
    Peso molecular:527.74
  • Laninamivir trifluoroacetate

    CAS:
    Laninamivir trifluoroacetate, a long-acting antiviral, treats and prevents Influenza A and B via nasal spray.
    Fórmula:C15H23F3N4O9
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:460.363
  • Neuraminidase-IN-18

    CAS:
    Neuraminidase-IN-18 (compound N5), a novel polyheterocyclic neuraminidase (NA) inhibitor, demonstrates significant inhibitory activity against H5N1 NA, with an IC 50 of 0.14 μM against the wild-type H5N1 NA and 0.27 μM against the H5N1-H274Y mutant NA. This compound effectively binds to NAs, inhibiting influenza virus replication at the cellular level [1].
    Fórmula:C22H18FN3O3S
    Cor e Forma:Solid
    Peso molecular:423.46
  • AV-5080

    CAS:
    AV-5080 is an orally active neuraminidase (neuraminidase) inhibitor that is utilized in the research of both Type A and Type B influenza viruses.
    Fórmula:C15H25FN4O4
    Cor e Forma:Solid
    Peso molecular:344.38
  • VV261

    CAS:
    VV261 is an orally active inhibitor of the Influenza Virus. It exhibits activity against the Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV) and the Lymphocytic Choriomeningitis Virus (LCMV), with EC50 values of 0.89 and 0.15, respectively.
    Fórmula:C28H34FN3O11
    Cor e Forma:Solid
    Peso molecular:607.58
  • Cap-dependent endonuclease-IN-5

    CAS:
    Cap-dependent endonuclease-IN-5 inhibits CEN and fights influenza with low toxicity and good in vivo properties.
    Fórmula:C27H21F2N3O4S2
    Cor e Forma:Solid
    Peso molecular:553.60
  • cis-RdRP-IN-5


    Cis-RdRP-IN-5 is an effective inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), employed in influenza virus research.
    Fórmula:C23H21N3O5
    Cor e Forma:Solid
    Peso molecular:419.43
  • Anti-Influenza agent 3


    Compound 11h: Potent, low-toxicity anti-influenza, inhibits M2 ion channels. EC50: 3.29μM (H3N2), 2.45μM (H1N1).
    Fórmula:C16H22ClNOS
    Cor e Forma:Solid
    Peso molecular:311.87
  • Cap-dependent endonuclease-IN-10

    CAS:
    Cap-dependent endonuclease-IN-10, with low toxicity & good stability, effectively inhibits flu viruses and shows promise against A, B, C types.
    Fórmula:C25H18F2N4O5S
    Cor e Forma:Solid
    Peso molecular:524.50
  • Cap-dependent endonuclease-IN-2


    Cap-dependent endonuclease-IN-2 strongly blocks influenza A virus RNA polymerase; it's a CEN inhibitor.
    Fórmula:C30H24FN3O7S
    Cor e Forma:Solid
    Peso molecular:589.59
  • RdRP-IN-4


    RdRP-IN-4, an oral arylbenzohydrazide, inhibits influenza A/B by targeting PB1 of RdRP, with EC50s of 53 nM (H1N1) and 20 nM (Flu B), and aids infected mice.
    Fórmula:C17H17Br2N3O2
    Cor e Forma:Solid
    Peso molecular:455.14
  • Cap-dependent endonuclease-IN-6

    CAS:
    Cap-dependent endonuclease-IN-6 (compound 13) is a Cap-dependent endonuclease (CEN) inhibitor that inhibits influenza virus.
    Fórmula:C23H21N3O3S
    Cor e Forma:Solid
    Peso molecular:419.5
  • trans-RdRP-IN-5


    Trans-RdRP-IN-5 is a potent inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), with applications in influenza virus research.
    Fórmula:C23H21N3O5
    Cor e Forma:Solid
    Peso molecular:419.43
  • Cap-dependent endonuclease-IN-7

    CAS:
    Cap-dependent endonuclease-IN-7, a potent CEN inhibitor, blocks viral mRNA synthesis and virus spread, with research use for influenza A, B, C.
    Fórmula:C36H28FN3O7S
    Cor e Forma:Solid
    Peso molecular:665.69
  • Cap-dependent endonuclease-IN-14

    CAS:
    Cap-dependent endonuclease-IN-14 hinders CEN and could treat influenza virus infections. (Patent CN113620948A, compound 1-c).
    Fórmula:C30H23FN2O6S
    Cor e Forma:Solid
    Peso molecular:558.58
  • Cap-dependent endonuclease-IN-25

    CAS:
    Cap-dependent endonuclease-IN-25 is a potent inhibitor of CEN, useful in studying Orthomyxoviridae viruses. (See WO2020075080A1, compound 4.)
    Fórmula:C25H25N3O3
    Cor e Forma:Solid
    Peso molecular:415.48
  • Cap-dependent endonuclease-IN-1

    CAS:
    Cap-dependent endonuclease-IN-1: potent, oral inhibitor with antiviral properties against influenza.
    Fórmula:C27H22F2N2O6S
    Pureza:99.53% - 99.61%
    Cor e Forma:Solid
    Peso molecular:540.54
  • UH15-38

    CAS:
    UH15-38 is a potent and selective RIPK3 inhibitor that blocks necroptosis in alveolar epithelial cells triggered by IAV, useful for studying lung inflammation.
    Fórmula:C26H27N5O2
    Pureza:99.85%
    Cor e Forma:Solid
    Peso molecular:441.53
  • FGI-106 tetrahydrochloride

    CAS:
    FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola
    Fórmula:C28H42Cl4N6
    Pureza:99.68%
    Cor e Forma:Solid
    Peso molecular:604.48