Filicinic acid based meroterpenoids from Hypericum elodeoides and their anti-Alzheimer’s disease effects

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Bioorganic Chemistry Pub Date : 2024-09-02 DOI:10.1016/j.bioorg.2024.107787
{"title":"Filicinic acid based meroterpenoids from Hypericum elodeoides and their anti-Alzheimer’s disease effects","authors":"","doi":"10.1016/j.bioorg.2024.107787","DOIUrl":null,"url":null,"abstract":"<div><p>(±)-Elodeoidileons A-L (<strong>1</strong>–<strong>12</strong>), 12 pairs of previously undescribed filicinic acid based meroterpenoids were isolated from <em>Hypericum elodeoides</em> with unique linear or angular 6/6/6 ring core. Modern spectroscopic techniques, modified Mosher’s method and quantum chemical calculations were used to identify the planner structures and configurations of <strong>1</strong>–<strong>12</strong>. Additionally, the potential biosynthetic pathways for <strong>1</strong>–<strong>12</strong> were anticipated. Moreover, biological activity assessments suggested that <strong>1a</strong>, <strong>5a</strong>, and <strong>11b</strong> could activate Retinoid X receptor-α (RXRα) transcription and enhance the ATP-binding cassette transporter A1 (ABCA1) protein’s expression. Fluorescence titration assay suggested that <strong>1a</strong> might have a direct interaction with the RXRα-LBD protein, with an estimated K<sub>d</sub> value of 5.85 μM. Moreover, molecular docking study confirmed the binding of <strong>1a</strong> to RXRα and further validated by cellular thermal shift assay (CETSA). Thus, compound <strong>1a</strong> may promote β-amyloid (Aβ) clearance by targeting RXRα and upregulating the expression of the ABCA1 protein, showing promise as anti-Alzheimer’s agent.</p></div>","PeriodicalId":257,"journal":{"name":"Bioorganic Chemistry","volume":null,"pages":null},"PeriodicalIF":4.5000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045206824006928","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

(±)-Elodeoidileons A-L (112), 12 pairs of previously undescribed filicinic acid based meroterpenoids were isolated from Hypericum elodeoides with unique linear or angular 6/6/6 ring core. Modern spectroscopic techniques, modified Mosher’s method and quantum chemical calculations were used to identify the planner structures and configurations of 112. Additionally, the potential biosynthetic pathways for 112 were anticipated. Moreover, biological activity assessments suggested that 1a, 5a, and 11b could activate Retinoid X receptor-α (RXRα) transcription and enhance the ATP-binding cassette transporter A1 (ABCA1) protein’s expression. Fluorescence titration assay suggested that 1a might have a direct interaction with the RXRα-LBD protein, with an estimated Kd value of 5.85 μM. Moreover, molecular docking study confirmed the binding of 1a to RXRα and further validated by cellular thermal shift assay (CETSA). Thus, compound 1a may promote β-amyloid (Aβ) clearance by targeting RXRα and upregulating the expression of the ABCA1 protein, showing promise as anti-Alzheimer’s agent.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
来自金丝桃的基于丝胶酸的 meroterpenoids 及其抗老年痴呆症的作用。
(±)-Elodeoidileons A-L (1-12),是从金丝桃中分离出的 12 对以前未曾描述过的以丝氨酸为基础的 meroterpenoids,具有独特的线性或角性 6/6/6 环核心。研究人员利用现代光谱技术、改进的莫舍尔法和量子化学计算,确定了 1-12 的平面结构和构型。此外,还预测了 1-12 的潜在生物合成途径。此外,生物活性评估表明,1a、5a 和 11b 可以激活视黄醇 X 受体-α(RXRα)的转录,并增强 ATP 结合盒转运体 A1(ABCA1)蛋白的表达。荧光滴定分析表明,1a 可能与 RXRα-LBD 蛋白有直接相互作用,其 Kd 值估计为 5.85 μM。此外,分子对接研究证实了 1a 与 RXRα 的结合,细胞热转移试验(CETSA)也进一步验证了这一点。因此,化合物 1a 可通过靶向 RXRα 和上调 ABCA1 蛋白的表达来促进 β 淀粉样蛋白(Aβ)的清除,有望成为抗老年痴呆症的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
期刊最新文献
Identification of novel RANKL inhibitors through in silico analysis Recent advances in the natural product analogues for the treatment of neurodegenerative diseases Impact of lipidation site on the activity of α-helical antimicrobial peptides Hyaluronan and Glucose Dual-targeting Probe: Synthesis and Application Discovery of N-Benzylpiperidinol derivatives as USP7 inhibitors against Hematology
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1