1H NMR conformational study of a variety of α-anomers of C5-substituted 2′-deoxyuridines: Comparison to their antiherpetic β counterparts

Biochemical and Biophysical Research Communications

Volumn 283, Issue 5, 2001, Pages 1142-1149

  Poznański, Jaroslaw ^a,b   Felczak, Krzysztof ^a   Bretner, Maria ^a   Kulikowski, Tadeusz ^a   Remin, Mieczyslaw ^c  

^a INSTITUTE OF BIOCHEMISTRY AND BIOPHYSICS   (Poland)

^b INSTITUTE OF PHYSICAL CHEMISTRY   (Poland)

^c UNIVERSITY OF WARSAW   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYURIDINE DERIVATIVE; METHYL GROUP; NUCLEOSIDE; ANTIVIRUS AGENT; DEOXYURIDINE; DRUG DERIVATIVE; HYDROGEN;

ANIMAL CELL; ANTINEOPLASTIC ACTIVITY; ARTICLE; CHEMICAL BOND; CONTROLLED STUDY; DRUG ACTIVITY; DRUG CONFORMATION; LEUKEMIA CELL; MOLECULAR INTERACTION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; CHEMICAL STRUCTURE; CHEMISTRY; COMPARATIVE STUDY; CONFORMATION; DRUG EFFECT; HERPES VIRUS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM;

ANTIVIRAL AGENTS; DEOXYURIDINE; HERPESVIRIDAE; HYDROGEN; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 0034741092     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.2001.4921     Document Type: Article

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