FKBP ligands as novel therapeutics for neurological disorders.

Abstract

Given their clinical importance for the treatment of acute and chronic neurodegenerative diseases in humans including nerve injuries (e.g. Alzheimer's disease, Parkinson's disease, diabetic neuropathy) a number of different approaches were pursued to obtain selectively acting FK506-binding protein (FKBP) ligands: computational methods and target-oriented screening of natural compound and synthetic product libraries. The resulting monofunctional ligands, which inhibit the peptidyl prolyl cis/trans isomerase activity of FKBPs, highlight the role of these enzymes in neuronal signaling. The exploration of the mechanisms of neuroregenerative and neuroprotective action of some of these compounds is the main focus of ongoing neuropharmaceutical research.

• Authors: C Christner, T Herdegen, G Fischer
• Journal: Mini reviews in medicinal chemistry (Mini Rev Med Chem) Vol. 1 Issue 4 Pg. 377-97 (Nov 2001) ISSN: 1389-5575 [Print] Netherlands
• PMID: 12369964 (Publication Type: Journal Article, Review)

Chemical References

• Enzyme Inhibitors
• Immunosuppressive Agents
• Ligands
• Calcium-Calmodulin-Dependent Protein Kinases
• Tacrolimus Binding Proteins
• Peptidylprolyl Isomerase

Topics

• Animals
• Calcium-Calmodulin-Dependent Protein Kinases (antagonists & inhibitors)
• Enzyme Inhibitors (pharmacology, therapeutic use)
• Humans
• Immunosuppressive Agents (pharmacology, therapeutic use)
• Ligands
• Nervous System Diseases (drug therapy)
• Peptidylprolyl Isomerase (antagonists & inhibitors)
• Signal Transduction (drug effects)
• Tacrolimus Binding Proteins (drug effects)