HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Inhibition of beta-amyloid-induced neurotoxicity by imidazopyridoindoles derived from a synthetic combinatorial library.

Abstract
Alzheimer's disease is a progressive neurodegenerative disorder characterized by the deposit of amyloid fibrils in the brain that result from the self-aggregative polymerization of the beta-amyloid peptide (Abeta). Evidence of a direct correlation between the ability of Abeta to form stable aggregates in aqueous solution and its neurotoxicity has been reported. The cytotoxic effects of Abeta have been attributed to the aggregation properties of a domain corresponding to the peptide fragment Abeta25-35. In an effort to generate novel inhibitors of Abeta neurotoxicity and/or aggregation, a mixture-based synthetic combinatorial library composed of 23 375 imidazopyridoindoles was generated and screened for inhibition of Abeta25-35 neurotoxicity toward the rat pheochromocytoma PC-12 cell line. The effect of the identified lead compounds on Abeta25-35 aggregation was then evaluated by means of circular dichroism (CD) and thioflavin-T fluorescence spectroscopy. Their activity against Abeta1-42 neurotoxicity toward the PC-12 cell line was also determined. The most active imidazopyridoindoles inhibited both Abeta25-35 and Abeta1-42 neurotoxicity in the low- to mid-micromolar range. Furthermore, inhibition of the random coil to beta-sheet transition and self-aggregation of Abeta25-35 was observed by CD and fluorescence spectroscopy, supporting the relationship between inhibition of the Abeta aggregation process and neurotoxicity.
AuthorsN Reixach, E Crooks, J M Ostresh, R A Houghten, S E Blondelle
JournalJournal of structural biology (J Struct Biol) Vol. 130 Issue 2-3 Pg. 247-58 (Jun 2000) ISSN: 1047-8477 [Print] United States
PMID10940229 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
CopyrightCopyright 2000 Academic Press.
Chemical References
  • Amyloid beta-Peptides
  • Benzothiazoles
  • Fluorescent Dyes
  • Indoles
  • Neurotoxins
  • Peptides
  • Thiazoles
  • thioflavin T
Topics
  • Amyloid beta-Peptides (antagonists & inhibitors, chemistry, toxicity)
  • Animals
  • Benzothiazoles
  • Cell Death (drug effects)
  • Circular Dichroism
  • Combinatorial Chemistry Techniques
  • Dimerization
  • Fluorescent Dyes
  • Humans
  • Indoles (chemistry, pharmacology)
  • Inhibitory Concentration 50
  • Nervous System Diseases (chemically induced)
  • Neurotoxins (pharmacology)
  • PC12 Cells (drug effects)
  • Peptides (antagonists & inhibitors, chemistry, toxicity)
  • Protein Structure, Secondary (drug effects)
  • Rats
  • Spectrometry, Fluorescence
  • Structure-Activity Relationship
  • Thiazoles

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: