基于配体的虚拟筛选和分子动力学模拟发现鞘氨醇-1-磷酸受体调节剂作为潜在的CHI3L1抑制剂

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-05-06 eCollection Date: 2025-05-20 DOI:10.1021/acsomega.5c01968
Elnaz Aledavood, Carmen Gil, Manuel Comabella, Ana Martinez
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引用次数: 0

摘要

多发性硬化症以中枢神经系统炎症、脱髓鞘和神经元变性为特征。目前的诊断和预后方法缺乏准确性,需要生物标志物来个性化治疗策略。几丁质酶3-样1 (CHI3L1)已成为潜在的预后标志物,其水平升高与疾病严重程度和复发风险相关。尽管其具有治疗潜力,但很少发现CHI3L1抑制剂。利用基于配体的虚拟筛选和分子动力学模拟,美国食品和药物管理局(Food and Drug administration)批准的药物已被筛选为CHI3L1抑制剂,最终目标是在MS和其他炎症性疾病中重新利用,提供有希望的治疗方法。本研究提示鞘氨醇-1-磷酸受体调节剂如芬戈莫德可能是CHI3L1的潜在抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of Sphingosine-1-Phosphate Receptor Modulators as Potential CHI3L1 Inhibitors by Ligand-Based Virtual Screening and Molecular Dynamics Simulations.

Multiple sclerosis is characterized by central nervous system inflammation, demyelination, and neuronal degeneration. Current diagnostic and prognostic methods lack precision, necessitating biomarkers for personalized treatment strategies. Chitinase 3-like 1 (CHI3L1) has emerged as a potential prognostic marker, with elevated levels correlating with disease severity and relapse risk. Despite its therapeutic potential, few CHI3L1 inhibitors have been identified. Using ligand-based virtual screening and molecular dynamics simulations, Food and Drug Administration-approved drugs have been screened as CHI3L1 inhibitors with the final goals of being repurposed in MS and other inflammatory diseases, offering promising therapeutic approaches. This investigation suggests that sphingosine-1-phosphate receptor modulators such as fingolimod could be potential inhibitors for CHI3L1.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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