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核心技术专利:CN118964589B侵权必究
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利用质谱和基于细胞的测定方法对 的代谢产物进行化学和生物学表征。

Chemical and Biological Characterization of Metabolites from Using Mass Spectrometric and Cell-Based Assays.

机构信息

Institute of the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Mirzo Ulugbek Str. 77, Tashkent 100170, Uzbekistan.

Tashkent Institute of Irrigation and Agricultural Mechanization Engineers, National Research University, Kori Niyazov Str. 39, Tashkent 100000, Uzbekistan.

出版信息

Biomolecules. 2024 Oct 11;14(10):1285. doi: 10.3390/biom14101285.


DOI:10.3390/biom14101285
PMID:39456218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505650/
Abstract

A comprehensive metabolite profiling of the medicinal plant using an UHPLC-ESI-MS/MS method is described for the first time. A total of 71 compounds were identified and annotated, the most common of which were flavonoids, triterpene glycosides, and ecdysteroids. The three major compounds schaftoside, 26-hydroxyecdysone, and silviridoside can be chosen as the markers for the assessment of the quality of preparations. The methanol extract and a variety of metabolites identified in were screened for their cytotoxic and Wnt pathway-inhibiting activities against triple-negative breast cancer (TNBC), the deadliest form of cancer in women. 2-Deoxy-20-hydroxyecdysone with submicromolar IC was identified as a result. The structure-activity relationship derived from the data from the in vitro proliferation assay showed that the hydroxyl group present at position C-2 of steroid core reduces the ecdysteroids' cytotoxicity against cancer cells.

摘要

首次采用 UHPLC-ESI-MS/MS 方法对药用植物 进行全面的代谢物分析。共鉴定和注释了 71 种化合物,其中最常见的是黄酮类、三萜糖苷和蜕皮甾酮。沙福索苷、26-羟基蜕皮甾酮和紫堇醇苷这三种主要化合物可以作为评估 制剂质量的标志物。对 甲醇提取物和多种代谢物进行了筛选,以评估其对三阴性乳腺癌(TNBC)的细胞毒性和 Wnt 通路抑制活性,这是女性最致命的癌症形式。结果发现,具有亚毫摩尔 IC 的 2-脱氧-20-羟基蜕皮甾酮是一种有效的抑制剂。从体外增殖试验数据中得出的构效关系表明,甾体核心 C-2 位上的羟基降低了蜕皮甾酮对癌细胞的细胞毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/59967797d18b/biomolecules-14-01285-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/ae3e34a2a47e/biomolecules-14-01285-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/7fc0e980494e/biomolecules-14-01285-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/59967797d18b/biomolecules-14-01285-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/ae3e34a2a47e/biomolecules-14-01285-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/7fc0e980494e/biomolecules-14-01285-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e88/11505650/59967797d18b/biomolecules-14-01285-g003.jpg

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Chemical and Biological Characterization of Metabolites from Using Mass Spectrometric and Cell-Based Assays.

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[2]
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[3]
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[4]
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引用本文的文献

[1]
Success and Controversy of Natural Products as Therapeutic Modulators of Wnt Signaling and Its Interplay with Oxidative Stress: Comprehensive Review Across Compound Classes and Experimental Systems.

Antioxidants (Basel). 2025-5-14

本文引用的文献

[1]
Integration of Wnt-inhibitory activity and structural novelty scoring results to uncover novel bioactive natural products: new Bicyclo[3.3.1]non-3-ene-2,9-diones from the leaves of .

Front Chem. 2024-4-4

[2]
Triterpenoid saponins from Psammosilene tunicoides and their antinociceptive activities.

Phytochemistry. 2023-10

[3]
New cyclic glycolipids from promote MCF-7 breast carcinoma cell apoptosis by cell cycle arrest and mitotic Mps1/TTK inhibition.

RSC Adv. 2023-6-20

[4]
Cells of the tumor microenvironment speak the Wnt language.

Trends Mol Med. 2023-6

[5]
Silviridoside: A New Triterpene Glycoside from with Promising Antioxidant and Enzyme Inhibitory Potential.

Molecules. 2022-12-11

[6]
Wnt-pathway inhibitors with selective activity against triple-negative breast cancer: From thienopyrimidine to quinazoline inhibitors.

Front Pharmacol. 2022-10-28

[7]
Isolation and Identification of Isocoumarin Derivatives With Specific Inhibitory Activity Against Wnt Pathway and Metabolome Characterization of .

Front Chem. 2021-8-12

[8]
Mining Natural Compounds to Target WNT Signaling: Land and Sea Tales.

Handb Exp Pharmacol. 2021

[9]
Optimization of the clofazimine structure leads to a highly water-soluble C3-aminopyridinyl riminophenazine endowed with improved anti-Wnt and anti-cancer activity in vitro and in vivo.

Eur J Med Chem. 2021-10-15

[10]
Proapoptotic and proautophagic activity of 20-hydroxyecdysone in breast cancer cells in vitro.

Chem Biol Interact. 2021-6-1

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