Inhibition of chymotrypsin and pancreatic elastase by 4H-3,1-benzoxazin-4-ones

J Enzyme Inhib. 1991;4(3):227-32. doi: 10.3109/14756369109035846.

Abstract

Eight 3,1-Benzoxazin-4-ones have been used to inactivate chymotrypsin and pancreatic elastase. Whereas 6,7-dimethoxy substitution only slightly decreased the acylation rate constant, the deacylation reaction was nearly unaffected. Bulky alkoxy groups in position 2 of the heterocyclic moiety were shown to increase enormously the acylation rate of chymotrypsin, but not that of elastase.

Publication types

  • Comparative Study

MeSH terms

  • Acylation
  • Binding, Competitive
  • Chymotrypsin / antagonists & inhibitors*
  • Kinetics
  • Oxazines / pharmacology*
  • Pancreatic Elastase / antagonists & inhibitors*
  • Structure-Activity Relationship

Substances

  • Oxazines
  • Chymotrypsin
  • Pancreatic Elastase