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Influenza Virus

Influenza Virus

The influenza virus is a member of the Orthomyxoviridae family of segmented, single-stranded, negatively charged RNA viruses. Three different influenza virus types—A, B, and C—are included in this group. The type A viruses infect both domesticated and wild birds, horses, swine, other mammals, and humans, while the type B and C viruses only affect humans.In the United States, seasonal epidemics of disease are brought on by human influenza A and B viruses almost every winter. An influenza pandemic can be brought on by the spread of a brand-new, radically different influenza virus. Infections with influenza type C are thought to only cause a mild respiratory illness and not epidemics. Each virus subtype has undergone mutation, resulting in a variety of strains with various levels of pathogenicity; some are pathogenic to one species but not to others, and some are pathogenic to several.

Influenza Virus related products

Structure Cat No. Product Name CAS No. Product Description
1,4-Epidioxybisabola-2,10-dien-9-one V52526 1,4-Epidioxybisabola-2,10-dien-9-one 170380-69-5 1,4-Epidioxybisabola-2,10-dien-9-one is an analogue of 1,4-epidioxy-bisabola-2,12-diene and can be extracted from Curcuma longa L.
2'-Deoxy-2'-fluorocytidine V52514 2'-Deoxy-2'-fluorocytidine 10212-20-1 2'-Deoxy-2'-fluorocytidine is a nucleoside analogue that is a potent inhibitor of Congo hemorrhagic fever virus (CCHFV) replication.
2′-Deoxy-2′-fluoroguanosine (2'-脱氧-2'-氟鸟苷；2'-氟脱氧鸟苷；2'-氟-2'-脱氧鸟苷) V53068 2'-Deoxy-2'-fluoroguanosine (2'-deoxy-2'-fluoroguanosine; 2'-fluorodeoxyguanosine; 2'-fluoro-2'-deoxyguanosine) 78842-13-4 2′-Deoxy-2′-fluoroguanosine, a nucleoside analog, is a potent inhibitor of influenza virus, with an EC90 value of <0.35 μM for influenza A and B viruses.
2'-Deoxy-2'-fluorouridine V52995 2'-Deoxy-2'-fluorouridine 784-71-4 2'-Deoxy-2'-fluorouridine can be used as an intermediate in the preparation /synthesis of anti-influenza virus reagents.
2'-Deoxy-2'-fluorouridine-d2 V52752 2'-Deoxy-2'-fluorouridine-d2 362049-50-1 2'-Deoxy-2'-fluorouridine-d2 is the deuterated form of 2'-Deoxy-2'-fluorouridine.
2,3-Dehydro-2-deoxy-N-acetylneuraminic acid (Neu5Ac2en; DANA) V41078 2,3-Dehydro-2-deoxy-N-acetylneuraminic acid (Neu5Ac2en; DANA) 24967-27-9 N-acetyl-2,3-dehydro-2-Deoxyneuraminic Acid (Neu5Ac2en) is a potent neuraminidase inhibitor.
3-Azaspiro[5.5]undecane hydrochloride (4,4-Pentamethylenepiperidine hydrochloride) V54336 3-Azaspiro[5.5]undecane hydrochloride (4,4-Pentamethylenepiperidine hydrochloride) 1125-01-5 3-Azaspiro[5.5]undecane (4,4-Pentamethylenepiperidine) HCl is an inhibitor (blocker/antagonist) of WT influenza A virus M2 (A/M2) with IC50 of 1 μM.
4-O-Methylepisappanol V54343 4-O-Methylepisappanol 112529-37-0 4-O-Methylepisappanol (compound 9) is a naturally occurring compound extracted from the heartwood of Caesarpinia sappan.
6-Azathymine V52486 6-Azathymine 932-53-6 6-Azathymine, the 6-nitrogen analog of thymine, is a potent inhibitor of D-3-aminoisobutyrate-pyruvate aminotransferase.
7,3',4'-Trihydroxy-3-benzyl-2H-chromene V52481 7,3',4'-Trihydroxy-3-benzyl-2H-chromene 1111897-60-9 7,3',4'-Trihydroxy-3-benzyl-2H-chromene is a reversible, noncompetitive neuraminidase (NA) inhibitor.
7-51A V77680 7-51A 7-51A is a potent PB2 inhibitor (antagonist) with a Kd of 1.64 nM as determined by ITC.
Anti-IAV agent 1 V78009 Anti-IAV agent 1 Anti-IAV agent 1 (Compound (R)-1a) is an orally bioactive anti-influenza A virus (IAV) agent with IC50s of 0.03 μM and 0.06 μM for IAV H1N1 and Oseltamivir-resistant IAV H1N1, respectively.
Anti-Influenza agent 4 V34840 Anti-Influenza agent 4 522625-85-0 Anti-Influenza agent 4 is a potent and specific inhibitor of influenza virus (influenza virus), with EC50 of 150 nM and 62 nM against A/Roma and A/Parma strains respectively.
Anti-Influenza agent 5 V79290 Anti-Influenza agent 5 Anti-Influenza agent 5 (Compound IIB-2) is a chalcone-like analogue that is an inhibitor (blocker/antagonist) of influenza nuclear export.
Antiviral agent 34 V34990 Antiviral agent 34 945152-88-5 antiviral compound 34 is a potent and orally bioactive antiviral against influenza A and B subtypes with EC50 of 0.8 nM for H1N1 proliferation.
Antiviral agent 35 V34992 Antiviral agent 35 2760972-52-7 antiviral compound 35 (compound 4d) is an orally bioavailable inhibitor of influenza virus that acts in the early stages of viral replication.
Antiviral agent 41 V76069 Antiviral agent 41 68622-73-1 antiviral compound 41 (compound 5) is a diarylheptane compound extracted from Artemisia officinale and displays potential antiviral effect against influenza viruses in vitro
Antiviral agent 43 V76068 Antiviral agent 43 2739990-96-4 antiviral compound 43 (compound 16) is a potent orally bioactive influenza A virus entry inhibitor.
Asp-Asp-Asp-Asp-Asp-Asp V53378 Asp-Asp-Asp-Asp-Asp-Asp 145224-96-0 Asp-Asp-Asp-Asp-Asp-Asp is a polyaspartic acid.
Asp-Asp-Asp-Asp-Asp-Asp TFA V78140 Asp-Asp-Asp-Asp-Asp-Asp TFA Asp-Asp-Asp-Asp-Asp-Asp TFA is a polyaspartic acid.
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