Influenza Virus
Influenza virus inhibitors are compounds that interfere with the replication and spread of influenza viruses. These inhibitors are vital in researching antiviral strategies, understanding the life cycle of the influenza virus, and developing effective treatments and vaccines. Influenza inhibitors can target various stages of the viral replication process, including viral entry, replication, and release. At CymitQuimica, we offer a diverse range of high-quality influenza virus inhibitors to support your research in virology, infectious diseases, and antiviral drug development.
Found 300 products of "Influenza Virus"
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Influenza virus-IN-7
CAS:Influenza virus-IN-7: oral endonuclease inhibitor for flu research.Formula:C29H26F2N4O7SColor and Shape:SolidMolecular weight:612.6Crystal Violet
CAS:Crystal Violet (Hexamethylpararosaniline chloride) is a triarylmethane dye that is a mixture of violet rosanilinis, with antibacterial and antifungal effects.Formula:C25H30ClN3Purity:99.6% - ≥98%Color and Shape:Greenish Free Flowing Powder Solid PowderMolecular weight:407.98P9R
CAS:P9R is an antiviral peptide with broad-spectrum activity against coronaviruses (SARS-CoV-2, MERS-CoV, and SARS-CoV), influenza A H1N1 virus (A(H1N1)pdm09), influenza A H7N9 virus (A(H7N9) virus), and rhinovirus. It binds directly to viruses and inhibits virus-host endosomal acidification. P9R significantly protects mice from infection by influenza A H1N1 virus (A(H1N1)pdm09) without leading to resistant viruses. P9R is applicable in studying pH-dependent respiratory viruses.Formula:C144H232N52O35S5Color and Shape:SolidMolecular weight:3412.03Neuraminidase-IN-16
Neuraminidase-IN-16 (43b) inhibits H5N1, H5N8, H1N1, H3N2, H5N1-H274Y, H1N1-H274Y neuraminidases; IC50: 0.031-10.08 μM.Formula:C26H35FN2O4Color and Shape:SolidMolecular weight:458.57Trifluoromethyl-tubercidin
CAS:TFMT blocks MTr1 at SAM-binding site, curbing influenza virus replication with low toxicity in mice.
Formula:C12H13F3N4O4Purity:99.85% - 99.9%Color and Shape:SoildMolecular weight:334.25ATV03
ATV03 is an antiviral agent exhibiting potent activity against both type A and type B influenza viruses. It inhibits the type A (H3N2) and type B influenza viruses with EC50 values of 0.78 nM and 2.02 nM, respectively. The mechanism of action of ATV03 involves the inhibition of the polymerase acidic protein (PA) and RNA-dependent RNA polymerase (RdRp), as well as the disruption of nucleoprotein, thereby exerting its antiviral effects against influenza.Formula:C24H20FN3O5Color and Shape:SolidMolecular weight:449.43CEF4
CAS:CEF4 is a peptide derived from amino acids (aa) 342-351 of the influenza A virus nucleocapsid protein.Formula:C53H93N15O13Purity:98%Color and Shape:SolidMolecular weight:1148.4Anti-IAV agent 1
Anti-IAV agent 1 -1a: Orally active, fights influenza A. IC50: 0.03μM for H1N1, 0.06μM for resistant strains.Formula:C28H28FN9O3Color and Shape:SolidMolecular weight:557.58Influenza HA (307-319)
CAS:Influenza Hemagglutinin is an HLA-DRB 0101-restricted epitope from influenza hemagglutinin (307-319).Formula:C69H118N18O19Purity:98%Color and Shape:SolidMolecular weight:1503.78HA-IN-1
HA-IN-1 (compound 5g), a high-affinity Hemagglutinin (HA) ligand, targets the trypsin cleavage site of HA to inhibit HA-mediated membrane fusion and decreaseFormula:C42H35NO6Purity:98%Color and Shape:SolidMolecular weight:649.73HAA-09
CAS:HAA-09: oral anti-influenza with EC50 of 0.03μM; inhibits PB2, IC50 0.06μM; non-toxic, blocks virus replication.Formula:C17H18F2N6O2Color and Shape:SolidMolecular weight:376.36Methyl brevifolincarboxylate
CAS:Methyl brevifolincarboxylate is an influenza inhibitor targeting PB2 with IC50s of 27.16μM (H1N1) and 33.41μM (H3N2), and has antioxidant activity.Formula:C14H10O8Color and Shape:SolidMolecular weight:306.22Herquline A
CAS:Herquline A, a P. herquei alkaloid, blocks influenza A-induced cell death (IC50 = 10 μg/ml) and viral replication; hinders ADP/PAF-induced platelet clumping.Formula:C19H26N2O2Color and Shape:SolidMolecular weight:314.429PROTAC Hemagglutinin Degrader-1
PROTAC Hemagglutinin Degrader-1 (V3) degrades influenza HA potently (DC50 1.44 μM) with broad-spectrum antiviral effects.Formula:C61H93N5O9SColor and Shape:SolidMolecular weight:1072.48PA (224-233), Influenza
CAS:PA (224-233), Influenza is a 10-aa peptide, which is a fragment of polymerase 2 protein in Influenza a virus.Formula:C53H80N14O17Purity:98%Color and Shape:SolidMolecular weight:1185.29Eckol
CAS:Eckol inhibits ultraviolet B-induced cell damage by a decrease in oxidative stress in human keratinocytes.Formula:C18H12O9Purity:98%Color and Shape:SolidMolecular weight:372.28Cobalt protoporphyrin IX
CAS:Cobalt Protoporphyrin IX serves as a potent, specific inducer of heme oxygenase-1 (HO-1) and demonstrates broad-spectrum antiviral effects against Influenza AFormula:C34H32CoN4O4Purity:98%Color and Shape:SolidMolecular weight:619.58Triperiden
CAS:Triperiden: an anticholinergic, anti-Parkinson's drug; inhibits influenza by blocking haemagglutinin changes.Formula:C21H30ClNOColor and Shape:SolidMolecular weight:347.93Oseltamivir-acetate
CAS:Oseltamivir-acetate, an impurity of Oseltamivir, is a recommended neuraminidase inhibitor for both the treatment and prophylaxis of influenza A and B[1][2].Formula:C18H30N2O5Color and Shape:SolidMolecular weight:354.44PB2
CAS:PB2 is a TCEP-like compound that boosts RGC survival post-axotomy, effective even in tiny amounts, and offers improved permeability and neuroprotection.Formula:C16H20BO2PColor and Shape:SolidMolecular weight:286.12
