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一种通过靶向THRβ有效治疗非酒精性脂肪性肝炎的哒嗪酮化合物。

A Pyridazinone Compound for Effectively Treating Non-alcoholic Steatohepatitis by Targeting THRβ.

作者信息

Cheng Hao, Wang Xiao-Bo, Zhi Ying, Liu Bo, Liu Na, Li Meng-Jun, Mu Yan-Ling

机构信息

School of Pharmacy and Pharmaceutical Sciences, Shandong First Medical University, Jinan, China.

Institute of Materia Medica, Shandong Academy of Medical Sciences, Jinan, China.

出版信息

Front Chem. 2022 May 10;10:888587. doi: 10.3389/fchem.2022.888587. eCollection 2022.

Abstract

Developing effective therapies and medicines to conquer nonalcoholic steatohepatitis (NASH) is of great significance for public health and is faced with a major challenge. The activation of the thyroid hormone receptor agonist THRβ could be regulated by target drugs that has brought huge potential to the treatment of NASH. In this work, pyridazinone compound YWS01125 was synthesized for the first time. In this study, an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for YWS01125 determination was established, and the pharmacokinetics of YWS01125 was evaluated. The half-life values (t1/2)of three different doses of YWS01125 was 189.12 ± 95.27, 152.64 ± 37.98, and 181.95 ± 64.25 min, respectively, and the tissue distribution studies demonstrated that YWS01125 was quickly distributed to various tissues. With successful application in the pharmacokinetics study of YWS01125, the UPLC-MS/MS method has shown characteristics of high sensitivity, rapidity, and good selectivity.

摘要

开发有效的疗法和药物来攻克非酒精性脂肪性肝炎(NASH)对公共卫生具有重大意义,且面临着一项重大挑战。甲状腺激素受体激动剂THRβ的激活可由靶向药物调控,这为NASH的治疗带来了巨大潜力。在这项工作中,首次合成了哒嗪酮化合物YWS01125。在本研究中,建立了一种用于测定YWS01125的超高效液相色谱-串联质谱(UPLC-MS/MS)方法,并对YWS01125的药代动力学进行了评估。三种不同剂量的YWS01125的半衰期值(t1/2)分别为189.12±95.27、152.64±37.98和181.95±64.25分钟,组织分布研究表明YWS01125能迅速分布到各个组织。随着在YWS01125药代动力学研究中的成功应用,UPLC-MS/MS方法显示出高灵敏度、快速性和良好选择性的特点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f95b/9127185/48aaf1df19b1/fchem-10-888587-g001.jpg

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