seco-1-Azacubane-2-carboxylic Acid: Derivative Scope and Comparative Biological Evaluation

J Org Chem. 2024 Jan 5;89(1):798-803. doi: 10.1021/acs.joc.3c02333. Epub 2023 Dec 22.

Abstract

The unusual and sterically constrained amino acid, seco-1-azacubane-2-carboxylic acid, was incorporated into a range of bioactive chemical templates, including enalaprilat, perindoprilat, endomorphin-2 and isoniazid, and subjected to biological testing. The endomorphin-2 derivative displayed increased activity at the δ opioid receptor, but a loss in activity was observed in the other cases, although human normal cell line evaluation suggests limited cytotoxic effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids
  • Carboxylic Acids*
  • Cell Line
  • Humans
  • Receptors, Opioid, mu* / chemistry
  • Receptors, Opioid, mu* / metabolism

Substances

  • Receptors, Opioid, mu
  • Carboxylic Acids
  • Amino Acids