Inhibitors of HIV protease: Unique non-peptide active site templates

Journal of Molecular Recognition

Volumn 9, Issue 2, 1996, Pages 139-142

  Tait, B D ^a   Domagala, J ^a   Ellsworth, E L ^a   Ferguson, D ^a   Gajda, C ^a   Hupe, D ^a   Lunney, E A ^a   Tummino, P J ^a  

^a PFIZER INC   (United States)

Author keywords

3 hydroxy cyclohex 2 enone; 4 hydroxy 5,6 dihydropyrone; 4 hydroxy 2( 1H) pyridinone; 4 hydroxy 5H furan 2 one; HIV protease; inhibitors; tetronic acids

Indexed keywords

FURAN DERIVATIVE; PROTEINASE; PROTEINASE INHIBITOR; PYRIDONE DERIVATIVE; PYRONE DERIVATIVE;

BINDING SITE; CHEMICAL STRUCTURE; CHEMISTRY; CONFERENCE PAPER; DRUG DESIGN; METABOLISM; PROTEIN CONFORMATION; STRUCTURE ACTIVITY RELATION;

BINDING SITES; DRUG DESIGN; FURANS; HIV PROTEASE; HIV PROTEASE INHIBITORS; MODELS, MOLECULAR; PROTEIN CONFORMATION; PYRIDONES; PYRONES; STRUCTURE-ACTIVITY RELATIONSHIP;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 0030111119     PISSN: 09523499     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1352(199603)9:2<139::AID-JMR249>3.0.CO;2-H     Document Type: Conference Paper

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