Design of small peptidomimetic HIV-1 protease inhibitors and prodrug forms

Letters in Peptide Science

Volumn 6, Issue 5-6, 1999, Pages 275-281

  Kiso, Yoshiaki ^a   Matsumoto, Hikaru ^a   Yamaguchi, Satoshi ^a   Kimura, Tooru ^a  

^a KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Acyl migration type prodrug; Anti HIV drug; Conjugate of HIV protease inhibitor with RT inhibitor; HIV protease inhibitor; KNI compound; Substrate transition state analog

Indexed keywords

3 AMINO 2 HYDROXY 4 PHENYLBUTYRIC ACID; ASPARTIC ACID; ASPARTIC PROTEINASE; CARBOXYL GROUP; DIPEPTIDE; HYDROXYL GROUP; PRODRUG; PROTEINASE INHIBITOR;

CHEMICAL STRUCTURE; CONFERENCE PAPER; ENZYME ACTIVE SITE; ENZYME INHIBITION; HUMAN IMMUNODEFICIENCY VIRUS; HYDROGEN BOND; NONHUMAN; PROTEINASE INHIBITION; SOLUBILITY; STEREOCHEMISTRY; VIRUS REPLICATION;

EID: 0032873518     PISSN: 09295666     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02443422     Document Type: Conference Paper

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