Some 6-aza-5-substituted-2'-deoxyuridines show potent and selective inhibition of herpes simplex virus type 1 thymidine kinase

Nucleosides and Nucleotides

Volumn 17, Issue 1-3, 1998, Pages 187-206

  Basnak, I ^a   Sun, M ^a   Hamor, T A ^a   Focher, F ^b   Verri, A ^b   Spadari, S ^b   Wroblowski, B ^c   Herdewijn, P ^c   Walker, R T ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b CNR   (Italy)

^c REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYURIDINE DERIVATIVE; THYMIDINE KINASE;

ANTIVIRAL ACTIVITY; ARTICLE; COMPETITIVE INHIBITION; CRYSTAL STRUCTURE; DRUG SYNTHESIS; ENZYME ACTIVE SITE; ENZYME DEGRADATION; ENZYME PHOSPHORYLATION; HELA CELL; HERPES SIMPLEX VIRUS 1; HUMAN; HUMAN CELL; MOLECULAR MODEL;

HERPES; HUMAN HERPESVIRUS 1;

EID: 0031912392     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328319808005169     Document Type: Article

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