Improved Muscarinic Antagonists as Anticholinesterase Antidotes

Abstract

Muscarinic antagonists play an important role in anticholinesterase agent therapy by reducing the response of muscarinic receptors to acetylcholine, acting synergistically with cholinesterase reactivators. Therapy with antagonists such as atropine is difficult to manage because of the toxicity of these compounds, atropine antagonizes the receptor whether or not acetylcholine levels are elevated. Our approach to the development of a better antidote is to design a molecule whose concentration and resulting muscarinic antagonist activity is controlled by the degree of cholinesterase inhibition, and thus by the need for the drug. This is accomplished by incorporating into the same molecule features that confer muscarinic antagonism and susceptibility to hydrolysis by cholinesterase. Such compounds should be rapidly degraded by cholinesterase to inactive products in a normal system, but should remain active when cholinesterase has been inhibited. As the cholinesterase activity recovers, the compounds should again be hydrolyzed. The proper combination of muscarinic antagonism and susceptibility to cholinesterase hydrolysis should allow these compounds to be used at higher doses with fewer side effects.

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Document Details

Document Type
Technical Report
Publication Date
Mar 28, 1991
Accession Number
ADA242697

Entities

People

  • Michael Tracy

Organizations

  • SRI International

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • 1-Ring Heterocyclic Compounds
  • Acetylcholinesterases
  • Acids
  • Alcohols
  • Biomedical Research
  • Carboxylic Acids
  • Chemical Synthesis
  • Chemical Warfare
  • Chemistry
  • Contracts
  • Enzyme Inhibitors
  • Hydrolysis
  • Materials
  • Nerve Agents
  • Organic Chemistry
  • Recrystallization
  • Rodents

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  • Neurotoxicology
  • Systems Analysis and Design