CAS 196618-13-0
:Oseltamivir
- 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3R,4R,5S)-
- 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, [3R-(3α,4β,5α)]-
- Ebilfumin
- Enfluvir
- Ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate
- GOP-A-Flu
- Gs 4104
- Oseltamivr
- Tamiflu-Free
- Tamvir
- Zinc 039295508
- ethyl (3R,4R,5S)-4-(acetylamino)-5-amino-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate
- Voir plus de synonymes
Oseltamivir
CAS :Formule :C16H28N2O4Degré de pureté :>98.0%(T)(HPLC)Couleur et forme :White to Light yellow to Light orange powder to crystalMasse moléculaire :312.41(3R,4R,5S)-Ethyl 4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-enecarboxylate
CAS :Formule :C16H28N2O4Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :312.4045Oseltamivir 100 µg/mL in Acetonitrile
CAS :Formule :C16H28N2O4Couleur et forme :Single SolutionMasse moléculaire :312.40Oseltamivir
CAS :Oseltamivir (GS 4104) is an orally active and highly potent viral neuraminidase (NA) with antiviral activity, inhibits A/H3N2, A/H1N2, A/H1N1 and influenza B viruses, and can be used in studies of influenza and pneumonia.Formule :C16H28N2O4Degré de pureté :99.28%Couleur et forme :SolidMasse moléculaire :312.4Oseltamivir
CAS :Applications Oseltamivir is an orally active inhibitor of influenza virus neuraminidase; converted in vivo to the active acid metabolite. An antiviral drug. It is a COVID19-related research product.
References Oliyai, R., et al.: Pharm. Res., 15, 1300 (1998), Kim, C.U., et al.: Med. Chem. Res., 8, 392 (1998), Hayden, F.G., et al.: N. Engl. J. Med., 341, 1336 (1999), Treanor, J.J., et al.: J. Am. Med. Assoc., 283, 1016 (2000)Formule :C16H28N2O4Couleur et forme :Light YellowMasse moléculaire :312.4Oseltamivir
CAS :Inhibitor of viral neuraminidase enzyme, effective against influenza A and B viruses. This antiviral compound inhibits neuraminidase-mediated cleavage of host cell sialic acids, which interact with newly synthesised virions from the host cell. This prevents virion budding from the host, resulting in inhibition of virion release and viral infection overall.
Formule :C16H28N2O4Degré de pureté :Min. 95 Area-%Couleur et forme :PowderMasse moléculaire :312.4 g/mol






