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Influenza virus

Products for  Influenza virus

  1. Cat.No. Product Name Information
  2. GC39464 α-Cyclodextrin α-Cyclodextrin is a multifunctional, soluble dietary fiber marketed for use as a fiber ingredient. α-Cyclodextrin  Chemical Structure
  3. GC45228 β-Cyclodextrin β-Cyclodextrin (β-CD) is a cyclic oligosaccharide that contains seven D-(+)-glucopyranose units and has been used to improve the aqueous solubility of various compounds, especially those containing a phenyl group. β-Cyclodextrin  Chemical Structure
  4. GC39271 (±)-Naringenin A citrusderived flavonoid (±)-Naringenin  Chemical Structure
  5. GC61931 2′-Deoxy-2′-fluoroguanosine 2′-Deoxy-2′-fluoroguanosine, a nucleoside analog, is a potent inhibitor of influenza virus strains, with an EC90 of <0.35 μM for influenza virus A and B strains. 2′-Deoxy-2′-fluoroguanosine  Chemical Structure
  6. GC61756 2'-Deoxy-2'-fluorocytidine 2'-Deoxy-2'-fluorocytidine, an nucleoside analog, is a potent inhibitor of Crimean-Congo hemorrhagic fever virus (CCHFV) replication. 2'-Deoxy-2'-fluorocytidine  Chemical Structure
  7. GC61824 2'-Deoxy-2'-fluorouridine 2'-Deoxy-2'-fluorouridine can be used as an intermediate for antiinfluenza virus agents synthesis. 2'-Deoxy-2'-fluorouridine  Chemical Structure
  8. GC34450 3,4'-Dihydroxyflavone

    3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid with antiviral activity against Influenza A virus.

    3,4'-Dihydroxyflavone  Chemical Structure
  9. GC35109 3-Deoxysappanchalcone 3-Deoxysappanchalcone is a naturally-occurring chalcone compound isolated from Caesalpinia sappan L. 3-Deoxysappanchalcone  Chemical Structure
  10. GC60031 6-Azathymine 6-Azathymine, a 6-nitrogen analog of thymine, is a potent D-3-aminoisobutyrate-pyruvate aminotransferase inhibitor. 6-Azathymine  Chemical Structure
  11. GC39655 ABMA ABMA is a broad-spectrum inhibitor of intracellular toxins and pathogens. ABMA  Chemical Structure
  12. GC14502 AEBSF.HCl

    AEBSF.HCl is a broad-spectrum irreversible inhibitor of serine proteases, which can inhibit chymotrypsin, kallikrein, plasmin, thrombin, trypsin and related thrombolytic enzymes.

    AEBSF.HCl  Chemical Structure
  13. GC50013 AG 1478 hydrochloride Highly potent EGFR-kinase inhibitor AG 1478 hydrochloride  Chemical Structure
  14. GC63814 Amantadine Amantadine (1-Adamantanamine) is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine  Chemical Structure
  15. GC10105 Amantadine HCl Amantadine (1-Adamantanamine) hydrochloride is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine HCl  Chemical Structure
  16. GC12900 Aprotinin

    A serine protease inhibitor

    Aprotinin  Chemical Structure
  17. GC13979 Arbidol HCl Arbidol HCl is a potent, orally active broad-spectrum antiviral with activity against a number of enveloped and non-enveloped viruses. Arbidol HCl  Chemical Structure
  18. GC35423 Atractylone Atractylone  Chemical Structure
  19. GC39699 Aurintricarboxylic acid Aurintricarboxylic acid is a nanomolar-potency, allosteric antagonist with selectivity towards αβ-methylene-ATP-sensitive P2X1Rs and P2X3Rs, with IC50s of 8.6 nM and 72.9 nM for rP2X1R and rP2X3R, respectively. Aurintricarboxylic acid  Chemical Structure
  20. GC46093 Azadirachtin B An azadirachtin with diverse biological activities Azadirachtin B  Chemical Structure
  21. GN10158 Baicalein Baicalein  Chemical Structure
  22. GC19055 Baloxavir Baloxavir is an anti-influenza agent extracted from patent WO 2017104691 A1. Baloxavir  Chemical Structure
  23. GC35465 Baloxavir marboxil A prodrug form of the antiviral baloxavir acid Baloxavir marboxil  Chemical Structure
  24. GC39347 Benzimidazole Benzimidazole  Chemical Structure
  25. GC50377 Brequinar sodium Potent and selective DHODH inhibitor Brequinar sodium  Chemical Structure
  26. GC43020 C12E8 C12E8 (C12E8) is an non-ionic detergent that can be used for membrane protein extraction. C12E8  Chemical Structure
  27. GC31953 Camphor ((±)-Camphor) Camphor ((±)-Camphor) ((±)-Camphor ((±)-Camphor)) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. Camphor ((±)-Camphor)  Chemical Structure
  28. GC35606 Carbodine Carbodine (Carbocyclic cytidine) is a broad-spectrum antiviral agent active against DNA viruses, (+)RNA viruses, (-)RNA viruses, paramyxo, rhabdo and (+/-)RNA viruses, targets CTP synthetase that converts UTP to CTP. Carbodine  Chemical Structure
  29. GC32841 Catechin ((+)-Catechin) Catechin ((+)-Catechin) ((+)-Catechin ((+)-Catechin)) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Catechin ((+)-Catechin)  Chemical Structure
  30. GC62116 CBS1117 CBS1117 is a virus entry inhibitor with an IC50 of 70 nM for influenza A virus, A/Puerto Rico/8/34 (H1N1). CBS1117  Chemical Structure
  31. GC35639 CEF1, Influenza Matrix Protein M1 58-66 CEF1, Influenza Matrix Protein M1 58-66 is an epitope derived from the matrix protein of the influenza A virus. CEF1, Influenza Matrix Protein M1 58-66  Chemical Structure
  32. GC32293 CEF3 CEF3 (SIIPSGPLK) corresponds to aa 13-21 of the influenza A virus M1 protein. CEF3  Chemical Structure
  33. GC32329 CEF6 CEF6 is a 9-aa-long peptide corresponding to aa 418-426 of the influenza A virus (H1N1) nucleocapsid protein. CEF6  Chemical Structure
  34. GC43228 Cephaeline Cephaeline is an alkaloid originally isolated from C. Cephaeline  Chemical Structure
  35. GC35653 Cephalotaxlen Cephalotaxlen ((-)-Cephalotaxlen) is an alkaloid that can be isolated from Cephalotaxus drupacea, with antileukemic and antiviral activities. Cephalotaxlen  Chemical Structure
  36. GC31707 Chebulagic acid Chebulagic acid is a COX-LOX dual inhibitor isolated from the fruits of Terminalia chebula Retz, on angiogenesis. Chebulagic acid  Chemical Structure
  37. GC16135 Cinanserin hydrochloride 5-HT2 antagonist Cinanserin hydrochloride  Chemical Structure
  38. GC60715 Cletoquine oxalate Cletoquine oxalate (Desethylhydroxychloroquine oxalate) is a major active metabolite of Hydroxychloroquine. Cletoquine oxalate  Chemical Structure
  39. GN10663 Coumarin Coumarin  Chemical Structure
  40. GC11687 Crystal Violet triarylmethane dye Crystal Violet  Chemical Structure
  41. GC14787 Curcumin A yellow pigment with diverse biological activities Curcumin  Chemical Structure
  42. GC40226 Curcumin-d6 Curcumin-d6 is intended for use as an internal standard for the quantification of curcumin by GC- or LC-MS. Curcumin-d6  Chemical Structure
  43. 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
  44. GN10697 Dehydroandrographolide Dehydroandrographolide  Chemical Structure
  45. GC35830 Dehydroandrographolide succinate Dehydroandrographolide succinate, extracted from herbal medicine Andrographis paniculata (Burm f) Nees, is widely used for the treatment of viral pneumonia and viral upper respiratory tract infections because of its immunostimulatory, anti-infective and anti-inflammatory effect. Dehydroandrographolide succinate  Chemical Structure
  46. GC38120 Dendrobine A sesquiterpenoid with anticancer activity Dendrobine  Chemical Structure
  47. GC33930 Desaminotyrosine (3-(4-Hydroxyphenyl)propionic acid) Desaminotyrosine (3-(4-Hydroxyphenyl)propionic acid) is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling. Desaminotyrosine (3-(4-Hydroxyphenyl)propionic acid)  Chemical Structure
  48. GC47192 Desethyl Hydroxychloroquine Desethyl Hydroxychloroquine (Desethylhydroxychloroquine) is a major active metabolite of Hydroxychloroquine. Desethyl Hydroxychloroquine  Chemical Structure
  49. GC39234 DHODH-IN-2 DHODH-IN-2  Chemical Structure
  50. GC39374 DHODH-IN-5 DHODH-IN-5  Chemical Structure
  51. GC39734 Diphyllin Diphyllin is an arylnaphthalene lignan isolated from Justicia procumbens and is a potent HIV-1 inhibitor with an IC50 of 0.38 μM. Diphyllin  Chemical Structure
  52. 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
  53. GC38409 Epigoitrin Epigoitrin  Chemical Structure
  54. GC17947 Famciclovir Anti-herpesvirus oral prodrug of penciclovir Famciclovir  Chemical Structure
  55. GC60840 FGI-106 tetrahydrochloride FGI-106 tetrahydrochloride is a potent and broad-spectrum inhibitor with inhibitory activity against multiple viruses. FGI-106 tetrahydrochloride  Chemical Structure
  56. GC63670 Ganoderic acid TR Ganoderic acid TR is a broad-spectrum inhibitor against influenza neuraminidases (NAs), particularly H5N1 and H1N1 neuraminidases. Ganoderic acid TR  Chemical Structure
  57. GN10428 Geniposide Geniposide  Chemical Structure
  58. GC38418 Germacrone A sesquiterpene with diverse biological activities Germacrone  Chemical Structure
  59. GC36143 Glabranine Glabranine, an flavonoid, is isolated from Tephrosia s. Glabranine  Chemical Structure
  60. GC41486 Glaucine Glaucine is an alkaloid originally isolated from G. Glaucine  Chemical Structure
  61. GC65043 Haemanthamine Haemanthamine is a crinine-type alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. Haemanthamine  Chemical Structure
  62. GP10138 hemagglutinin (332-340) [Influenza A virus] hemagglutinin (332-340) [Influenza A virus]  Chemical Structure
  63. GP10055 hemagglutinin precursor (114-122) amide [Influenza A virus] Partial antigenic glycoprotein hemagglutinin precursor (114-122) amide [Influenza A virus]  Chemical Structure
  64. GC17196 Hesperadin A multi-kinase inhibitor Hesperadin  Chemical Structure
  65. GC38430 Hyperoside Hyperoside  Chemical Structure
  66. GC36315 Influenza A NP(366-374) Strain A/PR/8/35 Influenza A NP(366-374) Strain A/PR/8/35 is an H2-Db-restricted epitope from Influenza A/PR/8/35 nucleoprotein. Influenza A NP(366-374) Strain A/PR/8/35  Chemical Structure
  67. GP10128 Influenza A virus fragment

    Leu-Lys-Phe-Ala-Phe-Ser-Met-Met

    Influenza A virus fragment  Chemical Structure
  68. GC36317 Influenza NP 147-155 Influenza NP 147-155 is a Kd restricted epitope from influenza nucleoprotein. Influenza NP 147-155  Chemical Structure
  69. 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
  70. 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
  71. GC30493 KIN1148 KIN1148, a small-molecule IRF3 agonist, is a novel influenza vaccine adjuvant found to enhance flu vaccine efficacy. KIN1148  Chemical Structure
  72. GC62720 Lactimidomycin Lactimidomycin is a glutarimide-containing compound isolated from Streptomyces. Lactimidomycin  Chemical Structure
  73. 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
  74. GC62251 Laninamivir octanoate Laninamivir octanoate (CS-8958), a prodrug of Laninamivir, is a long-acting neuraminidase (NA) inhibitor with anti-influenza virus activity. Laninamivir octanoate  Chemical Structure
  75. GC39123 Lapachol A naphthoquinone with diverse biological activities Lapachol  Chemical Structure
  76. GC36519 M2 ion channel blocker M2 ion channel blocker is capable of inhibiting and blocking the activity of M2 ion channel;Antiviral agent. M2 ion channel blocker  Chemical Structure
  77. GC36520 M2e, human M2e, human, consisting of the 23 extracellular residues of M2 (the third integral membrane protein of influenza A), has been remarkably conserved in all human influenza A, which is a valid and versatile vaccine candidate to protect against any strain of human influenza A. M2e, human  Chemical Structure
  78. 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
  79. GC61052 Methyl brevifolincarboxylate Methyl brevifolincarboxylate  Chemical Structure
  80. 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
  81. GC62162 Molnupiravir Molnupiravir (EIDD-2801) is an orally bioavailable prodrug of the ribonucleoside analog EIDD-1931. Molnupiravir  Chemical Structure
  82. GC13122 Moroxydine HCl Moroxydine HCl (ABOB hydrochloride) is a synthetic antiviral compound chemically belonging to the series of the heterocyclic biguanidines. Moroxydine HCl  Chemical Structure
  83. GC61127 N-Glycolylneuraminic acid A sialic acid N-Glycolylneuraminic acid  Chemical Structure
  84. GC46185 Nimbin A limonoid with diverse biological activities Nimbin  Chemical Structure
  85. GC11618 Nitazoxanide Antiprotozoal agent Nitazoxanide  Chemical Structure
  86. GC36746 Nitazoxanide D4 Nitazoxanide D4 (NTZ D4) is the deuterium labeled Nitazoxanide, which is an antiprotozoal agent. Nitazoxanide D4  Chemical Structure
  87. GC15303 Nucleozin An antiviral Nucleozin  Chemical Structure
  88. GC14780 Oseltamivir acid A neuraminidase inhibitor and antiviral Oseltamivir acid  Chemical Structure
  89. GC63326 Oseltamivir acid-d3 Oseltamivir acid D3 (GS 4071 D3) is a deuterium labeled Oseltamivir acid. Oseltamivir acid-d3  Chemical Structure
  90. GC15396 Oseltamivir phosphate Potent and selective inhibitor of the neuraminidase Oseltamivir phosphate  Chemical Structure
  91. GC62244 Oseltamivir-acetate Oseltamivir-acetate is an impurity of Oseltamivir. Oseltamivir-acetate  Chemical Structure
  92. GC64333 Oseltamivir-d5 phosphate Oseltamivir-d5 phosphate  Chemical Structure
  93. GC32332 PA (224-233), Influenza PA (224-233), Influenza is a 10-aa peptide, a fragment of polymerase 2 protein in influenza A virus. PA (224-233), Influenza  Chemical Structure
  94. GC11859 Peramivir An inhibitor of influenza neuraminidase Peramivir  Chemical Structure
  95. GC13110 Peramivir Trihydrate potent, specific influenza viral neuraminidase inhibitor Peramivir Trihydrate  Chemical Structure
  96. GC19295 Pimodivir Pimodivir is an orally bioavailable inhibitor of influenza A virus polymerases through interaction with the viral PB2 subunit. Pimodivir  Chemical Structure
  97. GC60296 Polygalasaponin XXXI Polygalasaponin XXXI (Onjisaponin F) is an effective adjuvant for intranasal administration of influenza Influenza hemagglutinin (HA) vaccine to protect influenza virus infection. Polygalasaponin XXXI  Chemical Structure
  98. GC36953 PP7 PP7 is a potent PB1-PB2 interaction inhibitor with an IC50 of 8.6 μM, and their inhibition against viral polymerase activity (IC50=9.5 μM). PP7  Chemical Structure
  99. GN10451 Psoralen Psoralen  Chemical Structure
  100. GC64254 Rifampicin-d4 Rifampicin-d4  Chemical Structure
  101. GC63911 Rifampicin-d8 Rifampicin-d8  Chemical Structure

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