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Benzamide derivatives as dual-action hypoglycemic agents that inhibit glycogen phosphorylase and activate glucokinase

  • Lei Zhang
  • , Honglin Li
  • , Qingzhang Zhu
  • , Jun Liu
  • , Ling Chen
  • , Ying Leng*
  • , Hualiang Jiang
  • , Hong Liu
  • *Corresponding author for this work
  • CAS - Shanghai Institute of Materia Medica
  • East China University of Science and Technology
  • China Pharmaceutical University

Research output: Contribution to journalArticlepeer-review

Abstract

A series of benzamide derivatives which can simultaneously inhibit glycogen phosphorylase (GP) and activate glucokinase (GK) were prepared and evaluated. The structure-activity relationships (SAR) of these compounds were also presented. Among these, compounds 12, 13l, 13q, and 13v showed moderate activities towards both GK and GP. Compound 13h inhibited hLGP with an IC50 of 8.95 μM and activated GK with an EC50 of 1.87 μM. The possible binding modes of compounds 12, 13l, 13h, and 13q with GP and GK were also explored by molecular docking simulation.

Original languageEnglish
Pages (from-to)7301-7312
Number of pages12
JournalBioorganic and Medicinal Chemistry
Volume17
Issue number20
DOIs
StatePublished - 15 Oct 2009
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Dual action
  • Glucokinase (GK) activators
  • Glycogen phosphorylase (GP) inhibitors
  • Type 2 diabetes

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