Characterization of thymol derivatives from Eupatorium fortunei Turcz. aerial parts

被引:4
作者
Nguyen-Ngoc, Hieu [1 ]
Trang, Bui Thi Thu [2 ]
Thu, Do Thi Hoai [3 ]
Nguyen, Huu Tung [1 ]
Hoang, Vu Dinh [4 ]
Tran, Quang De [5 ]
Nguyen, Tuan Ngoc [6 ]
Quang, Dang Ngoc [7 ]
Pham, Giang Nam [8 ]
Le Dang, Quang [9 ,10 ]
机构
[1] PHENIKAA Univ, Fac Pharm, Hanoi, Vietnam
[2] Hanoi Univ Ind, Fac Chem Technol, Hanoi, Vietnam
[3] Vietnam Acad Sci & Technol VAST, Ctr High Technol Dev, Hanoi, Vietnam
[4] Hanoi Univ Sci & Technol, Sch Chem Engn, Hanoi, Vietnam
[5] Can Tho Univ, Coll Nat Sci, Dept Chem, Can Tho, Vietnam
[6] Ind Univ Ho Chi Minh City, Inst Biotechnol & Food Technol, Ho Chi Minh, Vietnam
[7] Hanoi Natl Univ Educ, Fac Chem, Hanoi, Vietnam
[8] Univ Cote Azur, Nice Inst Chem, Nice, France
[9] VAST, Inst Trop Technol, Hanoi, Vietnam
[10] Grad Univ Sci & Technol, VAST, Hanoi, Vietnam
关键词
Eupatorium fortunei; thymol derivatives; alpha-glucosidase; acetylcholinesterase;
D O I
10.1080/14786419.2023.2172726
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
From the aerial parts of Eupatorium fortunei, four thymol derivatives (1-4) were isolated and structurally elucidated by NMR and mass spectroscopic methods. Of which, a new dimeric thymol derivative (1) was characterized and its absolute configuration was established by electronic circular dichroism quantum method. In addition, the 1D and 2D NMR as well as HR-ESI mass spectral data of 2 were provided for the first time. Compounds 2-4 were evaluated for their inhibitory activity against alpha-glucosidase and acetylcholinesterase enzymes. All tested compounds showed weak inhibition at the concentration range of 1-256 mu g/mL in both enzymatic assays.
引用
收藏
页码:2306 / 2312
页数:7
相关论文
共 16 条
  • [1] Dibenzofuran, 4-Chromanone, Acetophenone, and Dithiecine Derivatives: Cytotoxic Constituents from Eupatorium fortunei
    Chang, Chun-Hao
    Wu, Semon
    Hsu, Kai-Cheng
    Huang, Wei-Jan
    Chen, Jih-Jung
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (14)
  • [2] Eupatorium fortunei and Its Components Increase Antiviral Immune Responses against RNA Viruses
    Choi, Jang-Gi
    Lee, Heeeun
    Hwang, Youn-Hwan
    Lee, Jong-Soo
    Cho, Won-Kyung
    Ma, Jin Yeul
    [J]. FRONTIERS IN PHARMACOLOGY, 2017, 8
  • [3] Coumarins and Polar Constituents from Eupatorium triplinerve and Evaluation of Their α-Glucosidase Inhibitory Activity
    Do Thi Viet Huong
    Phan Minh Giang
    Vu Minh Trang
    [J]. JOURNAL OF CHEMISTRY, 2020, 2020
  • [4] Benzofuran derivatives from Eupatorium fortunei
    Jiang, Hai Xia
    Liu, Quan
    Gao, Kun
    [J]. NATURAL PRODUCT RESEARCH, 2008, 22 (11) : 937 - 941
  • [5] Targeted Isolation of Cytotoxic Sesquiterpene Lactones from Eupatorium fortunei by the NMR Annotation Tool, SMART 2.0
    Lee, Jiho
    Park, Jinyoung
    Kim, Juyeol
    Jeong, Birang
    Choi, Seong Yeon
    Jang, Hyeon Seok
    Yang, Heejung
    [J]. ACS OMEGA, 2020, 5 (37): : 23989 - 23995
  • [6] Pharmacological Properties and Molecular Mechanisms of Thymol: Prospects for Its Therapeutic Potential and Pharmaceutical Development
    Meeran, Mohamed Fizur Nagoor
    Javed, Hayate
    Al Taee, Hasan
    Azimullah, Sheikh
    Ojha, Shreesh K.
    [J]. FRONTIERS IN PHARMACOLOGY, 2017, 8
  • [7] National Institute of Medicinal Materials, 2006, MED PLANTS AN VIETN, P246
  • [8] 10-acetoxy-9-chloro-8,9-dehydrothymol and further thymol derivatives from Arnica sachalinensis
    Passreiter, CM
    Matthiesen, U
    Willuhn, G
    [J]. PHYTOCHEMISTRY, 1998, 49 (03) : 777 - 781
  • [9] The recent development of thymol derivative as a promising pharmacological scaffold
    Sahoo, Chita Ranjan
    Paidesetty, Sudhir Kumar
    Padhy, Rabindra Nath
    [J]. DRUG DEVELOPMENT RESEARCH, 2021, 82 (08) : 1079 - 1095
  • [10] Two new thymol derivatives from Eupatorium fortunei
    Shi, Jing
    Dai, Yan-peng
    Yuan, Min
    Sun, Xiao-man
    Song, Chuan-jie
    Liu, Yu-guo
    [J]. NATURAL PRODUCT RESEARCH, 2024, 38 (03) : 386 - 392