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Discovery of a Locally and Orally Active CXCL12 Neutraligand (LIT-927) with Anti-inflammatory Effect in a Murine Model of Allergic Airway Hypereosinophilia
Author(s) -
Pierre Regenass,
Dayana Abboud,
François Daubeuf,
Christine Lehalle,
Patrick Gizzi,
Stéphanie Riché,
Muriel HachetHaas,
François Rohmer,
Vincent Gasparik,
Damien Boeglin,
Jacques Haiech,
Tim Knehans,
Didier Rognan,
Denis Heissler,
Claire Marsol,
Pascal Villa,
JeanLuc Galzi,
Marcel Hibert,
Nelly Frossard,
Dominique Bonnet
Publication year - 2018
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/acs.jmedchem.8b00657
Subject(s) - hypereosinophilia , chemistry , chemokine , in vivo , chalcone , biological activity , eosinophil , chemokine receptor , pharmacology , in vitro , receptor , immunology , biochemistry , eosinophilia , stereochemistry , biology , microbiology and biotechnology , asthma
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.

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