Chemotaxonomic significance of coumarins and alkaloids in the leaves of Glehnia littoralis

被引:0
作者
Li, Sainan [1 ]
Tian, Shuo [1 ]
Park, Jisu [1 ]
Zhou, Wei [2 ]
An, Renbo [3 ]
Na, Minkyun [1 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Pharmacognosy Lab, 99 Daehak Ro, Daejeon 34134, South Korea
[2] Yanbian Univ, Key Lab Nat Med Changbai Mt, Minist Educ, Yanji, Peoples R China
[3] Yanbian Univ, Sch Pharmaceut Sci, Yanji, Peoples R China
基金
新加坡国家研究基金会;
关键词
Glehnia littoralis; Apiaceae; Chemotaxonomy; Coumarins; Alkaloids; SECONDARY METABOLITES; CHEMICAL-CONSTITUENTS; ACID-DERIVATIVES; FRUITS; GLUCOSIDE; CHROMONE; ROOTS; FURANOCOUMARINS; UMBELLIPRENIN; GLYCOSIDES;
D O I
10.1016/j.bse.2025.105013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A phytochemical study of Glehnia littoralis leaves led to the isolation of 27 compounds, including 12 coumarins (1-12), four benzofuran glucosides (13-16), two phenols (17-18), one lignan (19), three alkaloids (20-22), two chromone glycosides (23-24), and three caffeoylquinic acids (25-27). Their structures were confirmed using NMR spectroscopy, ESI-MS, and optical rotation data from previous literature. To the best of our knowledge, compounds 16, 19-21, and 26 have not been reported from the Apiaceae family, while nine compounds 12-15, 18, 23-25, and 27 were obtained from the genus Glehnia for the first time. Except for coumarins, the unique alkaloids indole-3-carbaldehyde (20), deoxyhyrtiosine A (21), and naphthisoxazol A (22) are characteristic constituents for the chemotaxonomy of G. littoralis.
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页数:4
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