Organocatalyzed Novel Synthetic Methodology for Highly Functionalized Piperidines as Potent α-Glucosidase Inhibitors

  • Ariba Farooq
  • , Lubna Shahazadi
  • , Marek Bajda
  • , Nisar Ullah
  • , Abdul Rauf
  • , Sohail Anjum Shahzad
  • , Ather Farooq Khan
  • , Muhammad Ashraf
  • , Muhammad Yar*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

An efficient atom-economic one-pot synthesis of highly functionalized piperidines was achieved by catalytic multicomponent reaction. A wide range of heterogeneous and homogenous catalysts were explored; however, promising results were achieved when a β-keto-ester was reacted with selected aromatic aldehydes and anilines by using N-acetyl glycine (NAG) as catalyst. The implication of this methodology is straightforward since the products were precipitated out from the reaction solution, eliminating the need of column chromatography purifications. The synthesized piperidines were screened against α-glucosidase inhibition, which revealed that these compounds were very active inhibitors, and some of the compounds showed even better inhibition than the reference compound, at low micromolar concentrations. In silico molecular modeling was also performed to investigate the binding modes of the compounds into the active sites of the target protein.

Original languageEnglish
Pages (from-to)724-732
Number of pages9
JournalArchiv der Pharmazie
DOIs
StatePublished - 1 Sep 2016

Bibliographical note

Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Keywords

  • 2,6-Substituted piperidines
  • Molecular modeling
  • N-acetyl glycine
  • Organocatalysis
  • α-Glucosidase

ASJC Scopus subject areas

  • Pharmaceutical Science
  • Drug Discovery

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