Discovery of a Locally and Orally Active CXCL12 Neutraligand (LIT-927) with Anti-inflammatory Effect in a Murine Model of Allergic Airway Hypereosinophilia

J Med Chem. 2018 Sep 13;61(17):7671-7686. doi: 10.1021/acs.jmedchem.8b00657. Epub 2018 Aug 28.

Abstract

We previously reported Chalcone-4 (1) that binds the chemokine CXCL12, not its cognate receptors CXCR4 or CXCR7, and neutralizes its biological activity. However, this neutraligand suffers from limitations such as poor chemical stability, solubility, and oral activity. Herein, we report on the discovery of pyrimidinone 57 (LIT-927), a novel neutraligand of CXCL12 which displays a higher solubility than 1 and is no longer a Michael acceptor. While both 1 and 57 reduce eosinophil recruitment in a murine model of allergic airway hypereosinophilia, 57 is the only one to display inhibitory activity following oral administration. Thereby, we here describe 57 as the first orally active CXCL12 neutraligand with anti-inflammatory properties. Combined with a high binding selectivity for CXCL12 over other chemokines, 57 represents a powerful pharmacological tool to investigate CXCL12 physiology in vivo and to explore the activity of chemokine neutralization in inflammatory and related diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry*
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Chemokine CXCL12 / chemistry
  • Chemokine CXCL12 / metabolism*
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Fluorescence Resonance Energy Transfer
  • Humans
  • Hypereosinophilic Syndrome / drug therapy*
  • Hypersensitivity / drug therapy
  • Hypersensitivity / etiology
  • Male
  • Mice, Inbred BALB C
  • Models, Molecular
  • Pyrimidinones / administration & dosage
  • Pyrimidinones / chemistry*
  • Pyrimidinones / metabolism
  • Pyrimidinones / pharmacokinetics
  • Pyrimidinones / pharmacology*
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • CXCR4 protein, human
  • Chemokine CXCL12
  • LIT-927
  • Pyrimidinones
  • Receptors, CXCR4