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New 3,4-seco-diterpene and coumarin derivative from the leaves of Trigonostemon flavidus Gagnep

Ban Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi, Viet Nam|
Phan Van (6506589541) | Nguyen Huy (57228066200); Kiem | Nguyen Xuan (22951466700); Hoang | Bui Huu (34772017200); Nhiem | Nguyen Chi (57190275334); Tai | Tran My (55645262700); Mai | Ninh Khac (8213048200); Linh Graduate University of Science and Technology, Vietnam Academy of Science and Technology (VAST), Hanoi, Viet Nam|

Natural Product Research Số 13, năm 2022 (Tập 36, trang 3247-3254)

ISSN: 14786419

ISSN: 14786419

DOI:

Tài liệu thuộc danh mục:

Article

English

Từ khóa: Coumarins; Diterpenes; Euphorbiaceae; Humans; Molecular Structure; Plant Leaves; 3 4 secoditerpene; coumarin derivative; diterpenoid; fraxidin; heterophypene; isofraxetin; plant extract; plant glycoside; scopoletin; trigonostemon flavidus extract; unclassified drug; coumarin derivative; Article; breast cancer; carbon nuclear magnetic resonance; cell viability; cytotoxicity; electrospray mass spectrometry; Fourier transform infrared spectroscopy; high performance liquid chromatography; infrared spectroscopy; lung cancer; MCF-7 cell line; nonhuman; nuclear magnetic resonance; nuclear magnetic resonance spectroscopy; Pam LU-1 cell line; plant leaf; proton nuclear magnetic resonance; SK-MEL-2 cell line; skin cancer; thin layer chromatography; Trigonostemon flavidus; chemical structure; chemistry; Euphorbiaceae; human; plant leaf
Tóm tắt tiếng anh
Two new compounds named trigoflavidus A (1) and trigoflavidus B (2), and eight known compounds, trigoflavidone (3), heterophypene (4), howpene C (5), 3,4-seco-sonderianol (6), trigonochinene C (7), fraxidin (8), isofraxidin (9), and isofraxetin (10) were isolated from the leaves of Trigonostemon flavidus Gagnep. by various chromatographic methods. Their chemical structures were elucidated via UV, IR, HR-ESI-MS and NMR spectroscopic methods and divided into two groups including six 3,4-seco-diterpenes (1, 3-7) and four coumarins (2, 8-10). Absolute configurations at stereocenters of compound 1 were confirmed by comparison of its CD spectra with those of the TD-DFT calculations. At a concentration of 30 µM, compounds 1–10 exhibited weak cytotoxic activity toward LU1, HepG2, MCF7, and SKMel2 human cell lines (cell viability all over 50%). © 2020 Informa UK Limited, trading as Taylor & Francis Group.

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