Inhibitors of Civ1 kinase belonging to 6-aminoaromatic-2-cyclohexyldiamino purine series as potent anti-fungal compounds

Biochim Biophys Acta. 2004 Mar 11;1697(1-2):211-23. doi: 10.1016/j.bbapap.2003.11.025.

Abstract

There is today a blatant need for new antifungal agents, because of the recent increase in life-threatening infections involving an ever-greater number of fungal strains. Fungi make extensive use of kinases in the regulation of essential processes, in particular the cell cycle. Most fungal kinases, however, are shared with higher eukaryotes. Only the kinases which have no human homologs, such as the histidine kinases, can be used as targets for antifungal drugs design. This review describes efforts directed towards the discovery of drugs active against a novel target, the atypical cell cycle kinase, Civ1.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology*
  • Cell Cycle Proteins / antagonists & inhibitors
  • Cyclin-Dependent Kinase-Activating Kinase
  • Cyclin-Dependent Kinases*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology
  • Fungal Proteins / antagonists & inhibitors
  • Fungi / drug effects
  • Fungi / enzymology
  • Fungi / physiology
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Purines / chemistry*
  • Purines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Antifungal Agents
  • Cell Cycle Proteins
  • Enzyme Inhibitors
  • Fungal Proteins
  • Purines
  • Protein Serine-Threonine Kinases
  • Cyclin-Dependent Kinases
  • purine
  • Cyclin-Dependent Kinase-Activating Kinase