The Synthesis and Evaluation of 15-Keto-PGB1 Analogues.

Abstract

The ethyl analogue, 3-(trans-3-keto-1-pentenyl)-2-ethyl-2-cyclopentenone, was prepared as a structurally more suitable model for the investigation of the base promoted conversion of 15-keto-PGB1 to an oligomeric mixture termed PGBx. Base treatment of the ethyl analogue results in the conversion to an oligomeric mixture capable of protecting against the loss of oxidative phosphorylation in isolated mitochondria without inhibition at higher concentrations as observed for PGBx. The chemistry of the oligomerization was investigated and has major implications for an understanding of the complexity of the oligomeric mixture PGBx. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 1981
Accession Number
ADA098304

Entities

People

  • George L. Nelson

Organizations

  • University of Saint Joseph

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Acids
  • Alcohols
  • Analogs
  • Chemistry
  • Chromatography
  • Complex Mixtures
  • Crystal Structure
  • Hydrochloric Acid
  • Hydroxides
  • Mass Spectrometry
  • Mitochondria
  • Molecular Weight
  • Reaction Time
  • Spectra
  • Spectrometry
  • Spectroscopy
  • Water

Fields of Study

  • Chemistry

Readers

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