Effect of hydroxyl group configuration in hydroxyethylamine dipeptide isosteres on HIV protease inhibition. Evidence for multiple binding modes

J Med Chem. 1991 Mar;34(3):1222-5. doi: 10.1021/jm00107a049.
No abstract available

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Chemical Phenomena
  • Chemistry
  • Dipeptides / chemistry*
  • Dipeptides / metabolism
  • Ethanolamines / chemistry*
  • Ethanolamines / metabolism
  • HIV Protease / metabolism
  • HIV Protease Inhibitors*
  • Hydrogen Bonding
  • Molecular Conformation
  • Molecular Sequence Data
  • Molecular Structure
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Dipeptides
  • Ethanolamines
  • HIV Protease Inhibitors
  • HIV Protease