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发现并早期临床开发 5-脂氧合酶激活蛋白抑制剂(AZD5718)用于治疗冠状动脉疾病。

Discovery and Early Clinical Development of an Inhibitor of 5-Lipoxygenase Activating Protein (AZD5718) for Treatment of Coronary Artery Disease.

出版信息

J Med Chem. 2019 May 9;62(9):4312-4324. doi: 10.1021/acs.jmedchem.8b02004. Epub 2019 Mar 26.

Abstract

5-Lipoxygenase activating protein (FLAP) inhibitors attenuate 5-lipoxygenase pathway activity and reduce the production of proinflammatory and vasoactive leukotrienes. As such, they are hypothesized to have therapeutic benefit for the treatment of diseases that involve chronic inflammation including coronary artery disease. Herein, we disclose the medicinal chemistry discovery and the early clinical development of the FLAP inhibitor AZD5718 (12). Multiparameter optimization included securing adequate potency in human whole blood, navigation away from Ames mutagenic amine fragments while balancing metabolic stability and PK properties allowing for clinically relevant exposures after oral dosing. The superior safety profile of AZD5718 compared to earlier frontrunner compounds allowed us to perform a phase 1 clinical study in which AZD5718 demonstrated a dose dependent and greater than 90% suppression of leukotriene production over 24 h. Currently, AZD5718 is evaluated in a phase 2a study for treatment of coronary artery disease.

摘要

5-脂氧合酶激活蛋白 (FLAP) 抑制剂可减弱 5-脂氧合酶途径的活性,减少促炎和血管活性白三烯的产生。因此,它们被认为对包括冠状动脉疾病在内的涉及慢性炎症的疾病具有治疗益处。在此,我们披露了 FLAP 抑制剂 AZD5718(12)的药物化学发现和早期临床开发。多参数优化包括在人全血中获得足够的效力,在保持代谢稳定性和 PK 特性的同时避开 Ames 致突变胺片段,使口服给药后能够达到临床相关的暴露量。与早期先导化合物相比,AZD5718 具有更好的安全性特征,使我们能够进行一项 1 期临床研究,该研究表明 AZD5718 在 24 小时内可剂量依赖性地抑制白三烯的产生,抑制率大于 90%。目前,AZD5718 正在进行一项 2a 期研究,用于治疗冠状动脉疾病。

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