[Alkyl and aryl derivatives of isoquinoline. II. Synthesis and pharmacologic activity of dialkylaminoalkyl esters of 1-chloro-3-carboxy-4-methylisoquinoline and the corresponding 4-phenyl derivative]

Farmaco Sci. 1984 Mar;39(3):217-28.
[Article in Italian]

Abstract

The synthesis of a series of dialkylaminoalkylic esters of 1-chloro-3-carboxy-4-methylisoquinoline and of 1-chloro-3-carboxy-4-phenylisoquinoline is described. The pharmacological activity of some of these compounds was studied. The morpholinoethylester of 1-chloro-3-carboxy-4-methylisoquinoline (VIIa), dimethylaminoethylester (VIIb) and diethylaminoethylester (VIIc) showed a good antispasmodic activity. 4-Phenyl-derivatives (XVa), (XVb), (XVc) were more active than analogous 4-methyl derivatives; particularly the diethylaminoethylester of 1-chloro-3-carboxy-4-phenylisoquinoline (XVc) showed an antagonist effect against spasmogens similar to that of papaverine.

Publication types

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

MeSH terms

  • Acetylcholine / antagonists & inhibitors
  • Analgesics / chemical synthesis
  • Animals
  • Anti-Inflammatory Agents / chemical synthesis
  • Barium / antagonists & inhibitors
  • Central Nervous System / drug effects
  • Chemical Phenomena
  • Chemistry
  • Guinea Pigs
  • Histamine Antagonists / chemical synthesis
  • In Vitro Techniques
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / pharmacology
  • Male
  • Mice
  • Motor Activity / drug effects
  • Parasympatholytics / chemical synthesis*
  • Rats
  • Rats, Inbred Strains

Substances

  • Analgesics
  • Anti-Inflammatory Agents
  • Histamine Antagonists
  • Isoquinolines
  • Parasympatholytics
  • Barium
  • Acetylcholine