The discovery of a novel series of glucokinase activators based on a pyrazolopyrimidine scaffold

Bioorg Med Chem Lett. 2012 Dec 15;22(24):7302-5. doi: 10.1016/j.bmcl.2012.10.090. Epub 2012 Oct 27.

Abstract

Glucokinase is a key enzyme in glucose homeostasis since it phosphorylates glucose to give glucose-6-phosphate, which is the first step in glycolysis. GK activators have been proven to lower blood-glucose, and therefore have potential as treatments for type 2 diabetes. Here the discovery of pyrazolopyrimidine GKAs is reported. An original singleton hit from a high-throughput screen with micromolar levels of potency was optimised to give compounds with nanomolar activities. Key steps in this success were the introduction of an extra side-chain, which increased potency, and changing the linking functionality from a thioether to an ether, which led to improved potency and lipophilic ligand efficiency. This also led to more stable compounds with improved profiles in biological assays.

MeSH terms

  • Dose-Response Relationship, Drug
  • Drug Discovery*
  • Enzyme Activation / drug effects
  • Glucokinase / metabolism*
  • High-Throughput Screening Assays
  • Models, Molecular
  • Molecular Structure
  • Pyrazoles / chemical synthesis
  • Pyrazoles / chemistry*
  • Pyrazoles / pharmacology*
  • Pyrimidines / chemical synthesis
  • Pyrimidines / chemistry*
  • Pyrimidines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Pyrazoles
  • Pyrimidines
  • Glucokinase