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Home >> Signaling Pathways >> Microbiology & Virology >> Influenza virus

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

    SDihydrogenistein, NSC 11855, NSC 34875, Salipurol

     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'-DHF

    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

    Pefabloc SC

     AEBSF.HCl is a broad-spectrum, irreversible inhibitor of serine proteases, capable of inhibiting trypsin, kallikrein, plasmin, thrombin, chymotrypsin, 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

    Adamantylamine, Aminoadamantane, NSC 83653

     Amantadine (1-Adamantanamine) hydrochloride is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine HCl Chemical Structure
  16. GC70262 Amitivir Amitivir (LY 217896), a thiadiazole derivative, possesses broad antiviral activity against orthomyxo- and paramyxoviruses. Amitivir Chemical Structure
  17. GC12900 Aprotinin

    Bovine Pancreatic Trypsin Inhibitor, BPTI

     Aprotinin, a naturally occurring serine protease inhibitor, saves lives and decreases the risk of stroke and repeat surgery for massive bleeding. Aprotinin Chemical Structure
  18. GC13979 Arbidol HCl

    Umifenovir hydrochloride

     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
  19. 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
  20. GC35423 Atractylone Atractylone Chemical Structure
  21. 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
  22. GC46093 Azadirachtin B

    Deacetylazadirachtinol, 3-Tigloylazadirachtol

     An azadirachtin with diverse biological activities Azadirachtin B Chemical Structure
  23. GN10158 Baicalein Baicalein (5,6,7-trihydroxyflavone) is a flavonoid compound with multiple biological activities. It is a xanthine oxidase inhibitor with an IC50 value of 3.12μM. Baicalein Chemical Structure
  24. GC19055 Baloxavir

    BXA, S-033447

     Baloxavir is an anti-influenza agent extracted from patent WO 2017104691 A1. Baloxavir Chemical Structure
  25. GC35465 Baloxavir marboxil

    BXM, S-033188

     A prodrug form of the antiviral baloxavir acid Baloxavir marboxil Chemical Structure
  26. GC39347 Benzimidazole Benzimidazole Chemical Structure
  27. GC50377 Brequinar sodium

    DuP-785, NSC 368390

     Potent and selective DHODH inhibitor Brequinar sodium Chemical Structure
  28. GC43020 C12E8

    Octaethylene Glycol Monododecyl Ether

     C12E8 (C12E8) is an non-ionic detergent that can be used for membrane protein extraction. C12E8 Chemical Structure
  29. 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
  30. 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
  31. GC32841 Catechin ((+)-Catechin) Catechin ((+)-Catechin) ((+)-Catechin ((+)-Catechin)) inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM. Catechin ((+)-Catechin) Chemical Structure
  32. 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
  33. 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
  34. GC32293 CEF3 CEF3 (SIIPSGPLK) corresponds to aa 13-21 of the influenza A virus M1 protein. CEF3 Chemical Structure
  35. 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
  36. GC43228 Cephaeline

    (-)-Cephaeline

     Cephaeline is an alkaloid originally isolated from C. Cephaeline Chemical Structure
  37. GC35653 Cephalotaxlen

    (-)-Cephalotaxine, NSC 128487, NSC 245454, ZINC19795976

     Cephalotaxlen ((-)-Cephalotaxlen) is an alkaloid that can be isolated from Cephalotaxus drupacea, with antileukemic and antiviral activities. Cephalotaxlen Chemical Structure
  38. 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
  39. GC71694 Chloroxylenol-d6 Chloroxylenol-d6 is the deuterium labeled Chloroxylenol. Chloroxylenol-d6 Chemical Structure
  40. GC16135 Cinanserin hydrochloride

    SQ 10,643

     5-HT2 antagonist Cinanserin hydrochloride Chemical Structure
  41. 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
  42. GC60715 Cletoquine oxalate Cletoquine oxalate (Desethylhydroxychloroquine oxalate) is a major active metabolite of Hydroxychloroquine. Cletoquine oxalate Chemical Structure
  43. GN10663 Coumarin Coumarin Chemical Structure
  44. GC11687 Crystal Violet triarylmethane dye Crystal Violet Chemical Structure
  45. GC14787 Curcumin

    Indian Saffron, Turmeric yellow

     A yellow pigment with diverse biological activities Curcumin Chemical Structure
  46. 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
  47. 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
  48. GN10697 Dehydroandrographolide Dehydroandrographolide Chemical Structure
  49. 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
  50. GC38120 Dendrobine

    (-)-Dendrobine

     A sesquiterpenoid with anticancer activity Dendrobine Chemical Structure
  51. 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
  52. GC47192 Desethyl Hydroxychloroquine

    Cletoquine 

     Desethyl Hydroxychloroquine (Desethylhydroxychloroquine) is a major active metabolite of Hydroxychloroquine. Desethyl Hydroxychloroquine Chemical Structure
  53. GC39234 DHODH-IN-2 DHODH-IN-2 Chemical Structure
  54. GC39374 DHODH-IN-5 DHODH-IN-5 Chemical Structure
  55. GC39734 Diphyllin

    NSC 309691

     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
  56. GC72450 Diridavumab Diridavumab is a monoclonal anti-HA stalk antibody. Diridavumab Chemical Structure
  57. 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
  58. GC38409 Epigoitrin

    Ba 51-090278, (R)-Goitrin

     Epigoitrin Chemical Structure
  59. GC17947 Famciclovir

    BRL 42810

     Anti-herpesvirus oral prodrug of penciclovir Famciclovir Chemical Structure
  60. 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
  61. GC72414 Firivumab Firivumab (CT-P22; CT120) is a human IgG1 monoclonal influenza A virus hemagglutinin (Anti-IAV HA) antibody. Firivumab Chemical Structure
  62. 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
  63. GC74551 Gedivumab

    MHAA4549A; RG7745

     Gedivumab (MHAA4549A; RG7745) is a human monoclonal antibody that targets influenza A virus (IAV) with high specificity. Gedivumab Chemical Structure
  64. GN10428 Geniposide Geniposide Chemical Structure
  65. GC38418 Germacrone

    (E,E)-Germacrone

     A sesquiterpene with diverse biological activities Germacrone Chemical Structure
  66. GC36143 Glabranine Glabranine, an flavonoid, is isolated from Tephrosia s. Glabranine Chemical Structure
  67. GC41486 Glaucine

    Boldine Dimethyl Ether, (+)-Glaucine, NSC 34396, 1,2,9,10-Tetramethoxyaporphine

     Glaucine is an alkaloid originally isolated from G. Glaucine Chemical Structure
  68. GC65043 Haemanthamine Haemanthamine is a crinine-type alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. Haemanthamine Chemical Structure
  69. GP10138 hemagglutinin (332-340) [Influenza A virus]

    H2N-Thr-Gly-Leu-Arg-Asn-Ile-Pro-Ser-Ile-OH

    hemagglutinin (332-340) [Influenza A virus] Chemical Structure
  70. GP10055 hemagglutinin precursor (114-122) amide [Influenza A virus]

    H2N-Tyr-Pro-Tyr-Asp-Val-Pro-Asp-Tyr-Ala-amide

    Partial antigenic glycoprotein hemagglutinin precursor (114-122) amide [Influenza A virus] Chemical Structure
  71. GC17196 Hesperadin A multi-kinase inhibitor Hesperadin Chemical Structure
  72. GC38430 Hyperoside

    Hyperoside, NSC 407304, Quercetin-3-O-galactoside

     Hyperoside is a NF-κB inhibitor, found from Hypericum monogynum. Hyperoside shows anti-tumor, antifungal, anti-inflammatory, anti-viral, and anti-oxidative activitie. Hyperoside Chemical Structure
  73. 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
  74. GP10128 Influenza A virus fragment

    H2N-Leu-Lys-Phe-Ala-Phe-Ser-Met-Met-OH

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

     Influenza A virus fragment Chemical Structure
  75. 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
  76. GC36317 Influenza NP 147-155 Influenza NP 147-155 is a Kd restricted epitope from influenza nucleoprotein. Influenza NP 147-155 Chemical Structure
  77. 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
  78. 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
  79. GC30493 KIN1148 KIN1148, a small-molecule IRF3 agonist, is a novel influenza vaccine adjuvant found to enhance flu vaccine efficacy. KIN1148 Chemical Structure
  80. GC62720 Lactimidomycin

    Lactimidomycin is a glutarimide-containing compound isolated from Streptomyces.

     Lactimidomycin Chemical Structure
  81. 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
  82. 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
  83. GC39123 Lapachol

    C.I. 75490, NSC 11905, NSC 629756

     A naphthoquinone with diverse biological activities Lapachol Chemical Structure
  84. GC74569 Lesofavumab

    MHAB5553A; RG70026

     Lesofavumab (MHAB5553A) is a human IgG1κ anti-influenza B virus antibody. Lesofavumab Chemical Structure
  85. 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
  86. 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
  87. 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
  88. GC61052 Methyl brevifolincarboxylate Methyl brevifolincarboxylate Chemical Structure
  89. 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
  90. GC62162 Molnupiravir

    EIDD-2801, β-D-N4-Hydroxycytidine-5′-isopropyl ester, MK-4482

     Molnupiravir (EIDD-2801) is an orally bioavailable prodrug of the ribonucleoside analog EIDD-1931. Molnupiravir Chemical Structure
  91. GC13122 Moroxydine HCl

    ABOB

     Moroxydine HCl (ABOB hydrochloride) is a synthetic antiviral compound chemically belonging to the series of the heterocyclic biguanidines. Moroxydine HCl Chemical Structure
  92. GC61127 N-Glycolylneuraminic acid

    Neu5Gc, N-glycolyl-Neuraminic Acid

     A sialic acid N-Glycolylneuraminic acid Chemical Structure
  93. 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
  94. GC46185 Nimbin A limonoid with diverse biological activities Nimbin Chemical Structure
  95. GC11618 Nitazoxanide

    NSC 697855, NTZ

     Antiprotozoal agent Nitazoxanide Chemical Structure
  96. GC36746 Nitazoxanide D4 Nitazoxanide D4 (NTZ D4) is the deuterium labeled Nitazoxanide, which is an antiprotozoal agent. Nitazoxanide D4 Chemical Structure
  97. GC15303 Nucleozin An antiviral Nucleozin Chemical Structure
  98. GC70932 Onradivir Onradivir is a potent anti-influenza virus agent. Onradivir Chemical Structure
  99. GC14780 Oseltamivir acid

    GS-4071, Ro 64-0802

     A neuraminidase inhibitor and antiviral Oseltamivir acid Chemical Structure
  100. GC63326 Oseltamivir acid-d3

    GS 4071-d3; Ro 64-0802-d3; Oseltamivir carboxylate-d3

     Oseltamivir acid D3 (GS 4071 D3) is a deuterium labeled Oseltamivir acid. Oseltamivir acid-d3 Chemical Structure
  101. GC15396 Oseltamivir phosphate

    GS4104, Ro 640796/002

     Potent and selective inhibitor of the neuraminidase Oseltamivir phosphate Chemical Structure

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