SAR comparative studies on pyrimido[4,5-b][1,4] benzothiazine derivatives as 15-lipoxygenase inhibitors, using ab initio calculations

J Mol Model. 2008 Jun;14(6):471-8. doi: 10.1007/s00894-008-0298-8. Epub 2008 Apr 19.

Abstract

The enzyme inhibitory activity of a new group of 2-substituted pyrimido[4,5-b][1,4]benzothiazines on soybean 15-lipoxygenase (15-LO) was evaluated and compared with those of their 4-methyl analogs using ab initio calculations. The results of these studies showed that the lack of 4-methyl substituent in the pyrimido[4,5-b][1,4] benzothiazine molecules greatly reduces their 15-LO inhibitory activities.

Publication types

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

MeSH terms

  • Arachidonate 15-Lipoxygenase / chemistry
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Glycine max / enzymology
  • Lipoxygenase Inhibitors*
  • Models, Molecular
  • Molecular Structure
  • Protein Conformation
  • Pyrimidines
  • Structure-Activity Relationship
  • Thiazines

Substances

  • Enzyme Inhibitors
  • Lipoxygenase Inhibitors
  • Pyrimidines
  • Thiazines
  • Arachidonate 15-Lipoxygenase