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厚朴酚及其半合成衍生物:抗癌机制、药代动力学及未来治疗潜力的全面综述

Magnolol and its semi-synthetic derivatives: a comprehensive review of anti-cancer mechanisms, pharmacokinetics, and future therapeutic potential.

作者信息

Rayamajhi Asmita, Gyawali Nisha, Karki Deepa, Pérez-Caltzontzin Luis E, Peña-Corona Sheila I, Cortés Hernán, Adhikari Achyut, Leyva-Gómez Gerardo, Uprety Yadav, Habtemariam Solomon, Kiyekbayeva Lashyn, Sharifi-Rad Javad

机构信息

Central Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.

Departamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México, 04510, México.

出版信息

Discov Oncol. 2025 May 7;16(1):683. doi: 10.1007/s12672-025-02409-2.

Abstract

In recent years, magnolol (MG), a natural active compound of polyphenolic nature, has garnered significant interest for its anti-cancer effects. Numerous studies conducted on cell lines and animal models have indicated a positive impact of administering drugs or semi-synthesized products derived from MG, including a decreased incidence of various cancers. This review aims to illustrate the underlying cellular and molecular basis of its actions. The article includes in-depth explanations of phytochemistry, semi-synthetic derivatives, bioavailability, pharmacokinetics, preclinical research, anti-tumor mechanisms, human clinical studies, toxicity, side effects, and safety. It also demonstrates that, in contrast to the wealth of synthetic medications, MG is highly effective against bladder, colon, gastric, skin, liver, lung, gallbladder, and prostate cancers. The findings of this review indicate that MG is a promising candidate as an anti-tumor agent, and future research should focus on developing new semi-synthetic derivative compounds with potential anti-tumor properties.

摘要

近年来,厚朴酚(MG)作为一种具有多酚性质的天然活性化合物,因其抗癌作用而备受关注。对细胞系和动物模型进行的大量研究表明,给予源自MG的药物或半合成产品具有积极影响,包括降低各种癌症的发病率。本综述旨在阐述其作用的潜在细胞和分子基础。文章深入解释了植物化学、半合成衍生物、生物利用度、药代动力学、临床前研究、抗肿瘤机制、人体临床研究、毒性、副作用和安全性。它还表明,与大量合成药物相比,MG对膀胱癌、结肠癌、胃癌、皮肤癌、肝癌、肺癌、胆囊癌和前列腺癌具有高效性。本综述的结果表明,MG是一种有前途的抗肿瘤药物候选物,未来的研究应专注于开发具有潜在抗肿瘤特性的新型半合成衍生物化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f77/12058641/06a5ab8a2072/12672_2025_2409_Fig1_HTML.jpg

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