Design, synthesis and structure-activity relationship studies of novel phenoxyacetamide-based free fatty acid receptor 1 agonists for the treatment of type 2 diabetes

Bioorg Med Chem. 2015 Oct 15;23(20):6666-72. doi: 10.1016/j.bmc.2015.09.010. Epub 2015 Sep 5.

Abstract

The free fatty acid receptor 1 (FFA1) has attracted extensive attention as a novel antidiabetic target in the last decade. Several FFA1 agonists reported in the literature have been suffered from relatively high molecular weight and lipophilicity. We have previously reported the FFA1 agonist 1. Based on the common amide structural characteristic of SAR1 and NIH screened compound, we here describe the continued structure-activity exploration to decrease the molecular weight and lipophilicity of the compound 1 series by converting various amide linkers. All of these efforts lead to the discovery of the preferable lead compound 18, a compound with considerable agonistic activity, high LE and LLE values, lower lipophilicity than previously reported agonists, and appreciable efficacy on glucose tolerance in both normal and type 2 diabetic mice.

Keywords: Amide linkers; FFA1 agonist; Ligand efficiency; OGTT; Type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetanilides / chemical synthesis
  • Acetanilides / chemistry
  • Acetanilides / pharmacology*
  • Animals
  • CHO Cells
  • Cricetulus
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Dose-Response Relationship, Drug
  • Drug Design*
  • Humans
  • Male
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Molecular Structure
  • Receptors, G-Protein-Coupled / agonists*
  • Structure-Activity Relationship

Substances

  • 2-(2-fluoro-4-(2-(m-tolyloxy)acetamido)phenoxy)acetic acid
  • Acetanilides
  • FFAR1 protein, human
  • Receptors, G-Protein-Coupled