H NMR study of the sugar pucker of 2′,3′-dideoxynucleosides with anti-human immunodeficiency virus (HIV) activity
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference19 articles.
1. Chemotherapeutic approaches to the treatment of the acquired immune deficiency syndrome (AIDS)
2. Clinical applications of 3′-azido-2′,3′- dideoxythymidine (AZT) and related dideoxynucleosides
3. AIDS politics change rules
4. NMR investigation on the structure and conformation of 3′-azido-2′,3′-dideoxyribosylthymine (AZT), an inhibitor of the HIV (AIDS virus)
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1. Nucleotide Sugar Pucker Preference Mitigates Excision by HIV-1 RT;ACS Chemical Biology;2015-07-22
2. THE SUGAR RING CONFORMATION OF 4 '-ETHYNYL-2-FLUORO-2 '-DEOXYADENOSINE AND ITS RECOGNITION BY THE POLYMERASE ACTIVE SITE OF HIV REVERSE TRANSCRIPTASE;CELL MOL BIOL;2011
3. An abasic site induces a bulged conformation in the single-stranded DNA trimer d(Ap(ab)pA). An NMR and model-building study;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Using conformationally locked nucleosides to calibrate the anomeric effect: implications for glycosyl bond stability;Tetrahedron;2010-08
5. NMR Studies for Mapping Structure and Dynamics of Nucleosides in Water;Annual Reports on NMR Spectroscopy;2010
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