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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T5186 | Oseltamivir acid | GS 4071,oseltamivir carboxylate,Ro 64-0802 | Influenza Virus , Drug Metabolite |
Oseltamivir acid (GS4071) is a potent influenza virus neuraminidase inhibitor and the prodrug of GS4071. | |||
T1486 | Oseltamivir phosphate | GS 4104 | Influenza Virus |
Oseltamivir phosphate (GS 4104) is the phosphate salt of oseltamivir, a synthetic derivative prodrug of ethyl ester with antiviral activity. By blocking neuraminidases on the surfaces of influenza viruses, oseltamivir in... | |||
T60663L | Oseltamivir acid methyl ester hydrochloride | Others | |
Oseltamivir acid methyl ester hydrochloride is a precursor form of oseltamivir acid. Oseltamivir acid methyl ester is converted to oseltamivir acid converted by carboxylesterase 1 (CES1). | |||
T33827 | Oseltamivir carboxylate HCl | Oseltamivir carboxylate(HCI),GS4071 HC,Oseltamivir carboxylate HCI,Oseltamivir carboxylate hydrochloride,Ro 64-0802 hydrochloride | |
Oseltamivir carboxylate is an active metabolite of oseltamivir phosphate (Tamiflu). | |||
T37510 | Oseltamivir-acetate | ||
Oseltamivir-acetate, an impurity of Oseltamivir, is a recommended neuraminidase inhibitor for both the treatment and prophylaxis of influenza A and B[1][2]. | |||
T60663 | Oseltamivir acid methyl ester | Others | |
Oseltamivir acid methyl ester is a precursor form of oseltamivir acid, that converts to oseltamivir acid by carboxylesterase 1(CES1). Oseltamivir acid is the neuraminidase inhibitor and antiviral agent [1]. | |||
T24428 | M090 | M 090,M-090 | |
M090 is a potent inhibitor against amantadine-resistant viruses, including the 2009 H1N1 pandemic strains and oseltamivir-resistant viruses. | |||
T61557 | Influenza A virus-IN-4 | ||
Influenza A virus-IN-4 (compound 23b), a derivative of Oseltamivir, is a highly effective neuraminidase inhibitor. It exerts potent inhibitory effects on influenza viruses [1]. | |||
T72717 | Anti-IAV agent 1 | ||
Anti-IAV Agent 1-1a is an orally administered compound effective against the Influenza A virus (IAV), demonstrating inhibitory concentration 50 (IC50) values of 0.03 μM and 0.06 μM for the H1N1 strain and the Oseltamivir... | |||
TN4108 | Ganoderic acid Z | Antifection | |
The binding affinities of ganoderic acid DM and ganoderic acid Z (ÎGbind, -16.83 and-10.99 kcal mol-1) are comparable to that of current commercial drug oseltamivir (-23.62 kcal mol-1);Ganoderic acid DM is a potential s... | |||
T83046 | Anti-Influenza agent 5 | Influenza Virus | |
Anti-Influenza agent 5 (Compound IIB-2), a chalcone-like derivative, serves as an influenza nuclear export inhibitor. It effectively inhibits oseltamivir-resistant strains and hinders viral proliferation by obstructing t... | |||
T37466 | CAY10766 | ||
CAY10766 is an antiviral compound.1It inhibits entry of influenza virus-like particles pseudotyped with hemagglutinin A (HA) from H5N1 influenza A virus into A549 cells (EC50= 0.24 μM). CAY10766 (1 μM) reduces H1N1 and H... | |||
T83742 | SBP1 TFA | Spike Binding Peptide 1 | |
Spike Binding Peptide 1 (SBP1), representing amino acids 21-43 of angiotensin-converting enzyme 2 (ACE2), has been utilized in a novel approach involving lipid nanoparticles (LNPs) encapsulated with oseltamivir phosphate... |