Nucleoside analogues as highly potent and selective inhibitors of herpes simplex virus thymidine kinase

Bioorganic and Medicinal Chemistry Letters

Volumn 11, Issue 13, 2001, Pages 1655-1658

  Martin, Joseph A ^a   Lambert, Robert W ^a   Merrett, John H ^a   Parkes, Kevin E B ^a   Thomas, Gareth J ^a   Baker, Stewart J ^a   Bushnell, David J ^a   Cansfield, Julie E ^a   Dunsdon, Stephen J ^a   Freeman, Andrew C ^a   Hopkins, Richard A ^a   Johns, Ian R ^a   Keech, Elizabeth ^a   Simmonite, Heather ^a   Walmsley, Andrea ^a   Wong Kai In, Philippe ^a   Holland, Mark ^a  

^a Welwyn Garden City Herts AL7 3AY UK ^*  (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

5' AMINO 2',5' DIDEOXY 5 ETHYLURIDINE; AMIDE; CARBOXYLIC ACID DERIVATIVE; DIHYDROANTHRACENE CARBOXYLIC ACID DERIVATIVE; NUCLEOSIDE ANALOG; THIOXANTHENE; THYMIDINE KINASE INHIBITOR; UNCLASSIFIED DRUG; URIDINE DERIVATIVE; XANTHINE;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; DRUG POTENCY; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; HERPES SIMPLEX VIRUS; HUMAN; HUMAN CELL; IC 50; NONHUMAN;

ENZYME INHIBITORS; SIMPLEXVIRUS; THYMIDINE KINASE; URIDINE;

HERPES; SIMPLEXVIRUS;

EID: 0035833021     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(01)00256-6     Document Type: Article

References (25)