Description
A prodrug form of adefovir; inhibits HBV DNA synthesis in HepG2 2.2.15 cells infected with HBV (EC50 = 0.517 μM); cytotoxic to HepG2 2.2.15 cells (CC50 = 540 μM); inhibits HBV replication in the liver of HBV transgenic mice (ED50 = 0.2 μmol/kg per day),,
Formal name: 2,2-dimethyl-propanoic acid, 1,1′-[[[[2-(6-amino-9H-purin-9-yl)ethoxy]methyl]phosphinylidene]bis(oxymethylene)] ester
Synonyms: GS 0840
Molecular weight: 501.5
CAS: 142340-99-6
Purity: ≥98%
Formulation: A crystalline solid