Hydroxytyrosol isolation, comparison of synthetic routes and potential biological activities

被引:2
|
作者
Wang, Enhui [1 ]
Jiang, Yanfei [1 ]
Zhao, Chunyue [1 ]
机构
[1] Beijing Qingyan Boshi Hlth Management Co Ltd, 8 Hangfeng Rd, Beijing, Peoples R China
来源
FOOD SCIENCE & NUTRITION | 2024年 / 12卷 / 10期
关键词
biocatalysis; biological activity; chemical synthesis; hydroxytyrosol; physical extraction; VIRGIN OLIVE OIL; VASCULAR ENDOTHELIAL-CELLS; MILL WASTE-WATER; NF-KAPPA-B; IN-VITRO; STAPHYLOCOCCUS-AUREUS; NATURAL ANTIOXIDANT; PHENOLIC-COMPOUNDS; OXIDATIVE STRESS; INDUCE APOPTOSIS;
D O I
10.1002/fsn3.4349
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Hydroxytyrosol (HT) is a polyphenol found in the olive plant (Olea europaea) that has garnered attention from the food, feed, supplement, and pharmaceutical industries. HT has evolved from basic separation and extraction to chemical and biocatalytic synthesis. The yield of HT can reach 1.93 g/L/h through chemical synthesis and 7.7 g/L/h through biocatalysis; however, both methods are subject to inherent limitations. Furthermore, the potential health benefits associated with HT have been highlighted, including its ability to act as an antioxidant, reduce inflammation, combat cancer and obesity, and exert antibacterial and antiviral effects. Its neuroprotective effects, skin protection, and wound healing capabilities are also discussed. Given these remarkable biological properties, HT stands out as one of the most extensively investigated natural phenols. This review highlights future methods and pathways for the synthesis of HT, providing insights based on its bioactivity characteristics, health benefits, and potential future applications. Hydroxytyrosol (HT) is a polyphenol extracted from olive plant and its byproduct. This review highlights methods and pathways for the synthesis of hydroxytyrosol, providing insights based on its bioactivity characteristics, health benefits, and potential future applications.image
引用
收藏
页码:6899 / 6912
页数:14
相关论文
共 50 条
  • [21] Synthetic polyamines: an overview of their multiple biological activities
    Minarini, Anna
    Milelli, Andrea
    Tumiatti, Vincenzo
    Rosini, Michela
    Bolognesi, Maria Laura
    Melchiorre, Carlo
    AMINO ACIDS, 2010, 38 (02) : 383 - 392
  • [22] BIOLOGICAL-ACTIVITIES OF SYNTHETIC LIPID A ANALOGS
    MATSUURA, M
    KUMAZAWA, Y
    KOJIMA, Y
    KUBOTA, Y
    HOMMA, JY
    KUSUMOTO, S
    SHIBA, T
    JAPANESE JOURNAL OF MEDICAL SCIENCE & BIOLOGY, 1984, 37 (04): : 187 - 188
  • [23] Biological activities of synthetic saponins and cardiac glycosides
    Takechi, M
    Doi, K
    Wakayama, Y
    PHYTOTHERAPY RESEARCH, 2003, 17 (01) : 83 - 85
  • [24] Biological activities of synthetic grammistins and analogous peptides
    Nami Sugiyama
    Mika Araki
    Yuji Nagashima
    Kazuo Shiomi
    Fisheries Science, 2006, 72 : 1114 - 1120
  • [25] Pyrrolopyrazine derivatives: synthetic approaches and biological activities
    Fateme Dehnavi
    Seyedeh Roya Alizadeh
    Mohammad Ali Ebrahimzadeh
    Medicinal Chemistry Research, 2021, 30 : 1981 - 2006
  • [26] Biological activities of synthetic grammistins and analogous peptides
    Sugiyama, Nami
    Araki, Mika
    Nagashima, Yuji
    Shiomi, Kazuo
    FISHERIES SCIENCE, 2006, 72 (05) : 1114 - 1120
  • [27] Synthetic polyamines: an overview of their multiple biological activities
    Anna Minarini
    Andrea Milelli
    Vincenzo Tumiatti
    Michela Rosini
    Maria Laura Bolognesi
    Carlo Melchiorre
    Amino Acids, 2010, 38 : 383 - 392
  • [28] Natural and synthetic xanthonolignoids: Chemistry and biological activities
    Pinto, MMM
    Sousa, EP
    CURRENT MEDICINAL CHEMISTRY, 2003, 10 (01) : 1 - 12
  • [29] Pyrrolopyrazine derivatives: synthetic approaches and biological activities
    Dehnavi, Fateme
    Alizadeh, Seyedeh Roya
    Ebrahimzadeh, Mohammad Ali
    MEDICINAL CHEMISTRY RESEARCH, 2021, 30 (11) : 1981 - 2006
  • [30] Salicylic Acid: Synthetic Strategies and Their Biological Activities
    Rosheen, Shivali
    Sharma, Shivali
    Utreja, Divya
    CHEMISTRYSELECT, 2023, 8 (13):