Crown nucleoside monophosphate diesters: a new class of nucleoside prodrugs
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Antiviral Activity Spectrum and Target of Action of Different Classes of Nucleoside Analogues
2. Commentary: Metabolic Impediments to the use of Nucleotide Derivatives to Circumvent Resistance to Purine and Pyrimidine Analogs
3. Synthesis and anti-HIV evaluation of D4T and D4T 5'-monophosphate prodrugs
4. Diaryl phosphate derivatives act as pro-drugs of AZT with reduced cytotoxicity compared to the parent nucleoside
5. Synthesis and antiviral activity of 3′-azido-3′-deoxythymidine triphosphate distearoylglycerol: a novel phospholipid conjugate of the anti-HIV agent AZT
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1. ChemInform Abstract: Crown Nucleoside Monophosphate Diesters: A New Class of Nucleoside Prodrugs.;ChemInform;2010-08-05
2. Synthesis and NMR characterization of a novel crown-ether ring-fused uridine analogue;Tetrahedron;2010-08
3. Synthesis and Cytotoxicity of Derivatives of Fluorouracil Conjugated with Three-membered Ring;Chinese Journal of Chemistry;2009-07
4. Structural features of the adenosine conjugate in means of vibrational spectroscopy and DFT;Biophysical Chemistry;2009-06
5. Approaches to the Synthesis of Conjugates of Phosphocavitands and Natural Compounds;Phosphorus, Sulfur, and Silicon and the Related Elements;2003-07
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