2-Aminothiophene-3-carboxylates and carboxamides as adenosine A1 receptor allosteric enhancers

Bioorg Med Chem. 2006 Apr 1;14(7):2358-65. doi: 10.1016/j.bmc.2005.11.018. Epub 2005 Nov 28.

Abstract

Three series of 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene and 2-amino-5,6,7,8-tetrahydrocyclohepta[b]thiophenes with 3-carboxylates and carboxamides have been prepared using the Gewald synthesis and evaluated as A(1)AR allosteric enhancers. The structure-activity relationships of these classes of compound are described. A number of compounds, notably 7b, are more potent and efficacious than PD81,723 (1).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allosteric Regulation / drug effects
  • Amides / chemical synthesis
  • Amides / chemistry
  • Amides / pharmacology*
  • Carboxylic Acids / chemical synthesis
  • Carboxylic Acids / chemistry
  • Carboxylic Acids / pharmacology*
  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Structure
  • Receptor, Adenosine A1 / drug effects*
  • Structure-Activity Relationship
  • Thiophenes / chemical synthesis
  • Thiophenes / chemistry
  • Thiophenes / pharmacology*

Substances

  • Amides
  • Carboxylic Acids
  • Receptor, Adenosine A1
  • Thiophenes