Design, synthesis and in vitro evaluation of l-amino acid esters prodrugs of acyclic nucleoside phosphonates as anti-HBV agent
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference12 articles.
1. Clinical Potential of the Acyclic Nucleoside Phosphonates Cidofovir, Adefovir, and Tenofovir in Treatment of DNA Virus and Retrovirus Infections
2. Antiviral acyclic nucleoside phosphonates structure activity studies
3. Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability
4. Synthesis and evaluation of novel amidate prodrugs of PMEA and PMPA
5. Design, Synthesis, and Characterization of a Series of Cytochrome P450 3A-Activated Prodrugs (HepDirect Prodrugs) Useful for Targeting Phosph(on)ate-Based Drugs to the Liver§
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1. Diversity oriented efficient access of trisubstituted purines via sequential regioselective Mitsunobu coupling and SNAr based C6 functionalizations;Tetrahedron;2013-01
2. Encapsulation of adefovir bis(l-leucine propyl)ester pro-virucide in cucurbit[7]uril and its activity against tobacco mosaic virus;Supramolecular Chemistry;2012-11-19
3. Synthesis, anti-HBV activity and renal cell toxicity evaluation of mixed phosphonate prodrugs of adefovir;European Journal of Medicinal Chemistry;2012-03
4. Design, synthesis and in vitro evaluation of mono (2, 2, 2-trifluoroethyl) esters, mono l-amino acid ester prodrugs of acyclic nucleoside phosphonates as anti-HBV agents;Chinese Chemical Letters;2011-12
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