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发现一种局部和口服活性的 CXCL12 中和配体(LIT-927),在变应性气道嗜酸性粒细胞增多症的小鼠模型中具有抗炎作用。

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

机构信息

Laboratoire d'Innovation Thérapeutique , Faculté de Pharmacie, UMR7200 CNRS/Université de Strasbourg , 74 route du Rhin , 67401 Illkirch , France.

Labex MEDALIS , Université de Strasbourg , 67000 Strasbourg , France.

出版信息

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.

摘要

我们之前报道过查尔酮-4(1),它可以与趋化因子 CXCL12 结合,而不是与其同源受体 CXCR4 或 CXCR7 结合,并中和其生物学活性。然而,这种中性配体存在一些局限性,如化学稳定性差、溶解度低和口服活性差。在此,我们报告了嘧啶酮 57(LIT-927)的发现,它是一种新型的 CXCL12 中性配体,其溶解度高于 1,且不再是迈克尔受体。虽然 1 和 57 都能减少过敏性气道嗜酸性粒细胞增多症小鼠模型中的嗜酸性粒细胞募集,但只有 57 在口服给药后显示出抑制活性。因此,我们在这里将 57 描述为第一个具有抗炎特性的口服活性 CXCL12 中性配体。57 对 CXCL12 具有很高的结合选择性,超过其他趋化因子,它代表了一种强大的药理学工具,可用于研究体内 CXCL12 生理学,并探索趋化因子中和在炎症和相关疾病中的活性。

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