Inhibition of human leukocyte elastase. 3. Synthesis and activity of 3'-substituted cephalosporins

J Med Chem. 1990 Sep;33(9):2529-35. doi: 10.1021/jm00171a030.

Abstract

Several 3'-substituted cephalosporin sulfones were synthesized from 3-(hydroxymethyl)cephalosporin, which was prepared by Ti(OiPr)4 hydrolysis of the corresponding acetate. A method was also developed to prepare a 3-vinylcephalosporin. Some of these compound were found to be potent time-dependent inhibitors of human leukocyte elastase (HLE). The HLE inhibitory activity was correlated with sigma 1 and it was concluded that the potency was determined by the electron-withdrawing ability as well as the size of the substituent. A mechanism for inhibition of HLE by cephalosporin sulfones is proposed.

MeSH terms

  • Cephalosporins / chemical synthesis*
  • Cephalosporins / pharmacology
  • Chemical Phenomena
  • Chemistry
  • Humans
  • Leukocyte Elastase
  • Pancreatic Elastase / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Sulfones / chemical synthesis
  • Sulfones / pharmacology

Substances

  • Cephalosporins
  • Sulfones
  • Pancreatic Elastase
  • Leukocyte Elastase