Affiliation:
1. Institute of Marine Biochemistry VAST 18 Hoang Quoc Viet, Cau Giay Hanoi 10072 Vietnam
2. Chuncheon Center Korea Basic Science Institute (KBSI) Gib-Hyun-Kwan 1 Kangwondaehak-gil Chuncheon-si Gangwon-do 24341 Korea
3. New Drug Development Center Daegu Gyeongbuk Medical Innovation Foundation Daegu 41061 Korea
4. VNU University of Science Vietnam National University 334 Nguyen Trai Thanh Xuan Hanoi Vietnam
5. Graduate University of Science and Technology VAST 18 Hoang Quoc Viet, Cau Giay Hanoi 10072 Vietnam
Abstract
AbstractVitex trifolia L. is a medicinal plant and widely distributed in the northern mountainous areas of Vietnam. Phytochemical study on the fruits of this plant led to the isolation of nine iridoid derivatives (1–9) including three undescribed compounds (1–3). Their structures were elucidated to be 3′′‐hydroxyscrophuloside A1 (1), 3′′‐hydroxycallicoside D (2), 2′‐p‐hydroxybenzoylaucubin (3), 6′‐p‐hydroxybenzoylmussaenosidic acid (4), nishindaside (5), agnuside (6), 10‐O‐vanilloylaucubin (7), 6′‐O‐p‐hydroxybenzoyl‐gardoside (8), and buddlejoside B (9) based on extensive analyses of HR‐ESI‐MS, 1D and 2D NMR spectra. Compounds 1, 2, 4, and 8 significantly posessed anti‐barterial activity against Enterococcus faecalis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa strains with MIC values in range of 16–64 μg/mL. At concentration of 20 μM, compounds 1–9 did not show cytotoxic effects against human lung cancer cells (PC9).
Subject
Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering
Cited by
1 articles.
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