A method and composition for treating viral infections by liposome-encapsulation of the anti-viral compounds phosphonoformate and phosponoacetate.
The invention provides methods for treating HIV infection in a subject in need thereof comprising lipid analogs of phosphonoformate-containing pharmaceutically active compounds.
TPFA is demonstrated to be at least as effective as PFA in inhibiting CMV viral replication, while having substantially improved bioavailability relative thereto.
The present invention pertains to novel compounds which are derivatives of phosphonoformic acid, processes for their synthesis and their use as antiviral agents.
Preparation of phosphonoformic acid analogues containing one, two, three, or more sulfur atoms are described, with specific examples.
Methods and compositions for use in inhibiting CMV replication in mammalian patients, wherein an effective amount of TPFA is administered to a patient in need of such treatment.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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