The history of N-methanocarbathymidine: The investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent-Reference-Cited by-同舟云学术

The history of N-methanocarbathymidine: The investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent

Published:2006-09 Issue:2-3 Volume:71 Page:268-275
ISSN:0166-3542
Container-title:Antiviral Research
language:en
Short-container-title:Antiviral Research

Author:

Marquez Victor E.,Hughes Stephen H.,Sei Shizuko,Agbaria Riad

Publisher

Elsevier BV

Subject

Virology,Pharmacology

Reference24 articles.

1. 4′,6′-Methano carbocyclic thymidine. A conformationally constrained building block for oligonucleotides;Altmann;Tetrahedron Lett.,1994

2. 1′,6′-Methano carbocyclic thymidine. Synthesis, X-ray crystal structure, and effect on nucleic-acid duplex stability;Altmann;Tetrahedron Lett.,1994

3. Fixed conformation nucleoside analogs effectively inhibit excision-proficient HIV-1 reverse transcriptases;Boyer;J. Mol. Biol.,2005

4. Conformationally locked carbocyclic nucleosides built on a bicyclo[3.1.0]hexane template with a fixed Southern conformation. Synthesis and antiviral activity;Ezzitouni;J. Chem. Soc. Perkin Trans. I,1997

5. Dynamics of the antiviral activity of N-methanocarbathymidine against herpes simplex virus type 1 in cell culture;Huleihel;Int. J. Antimicrob. Agents,2005

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