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Three Undescribed Iridoid Derivatives Isolated from the Fruits of Vitex trifolia with Their Cytotoxic and Antimicrobial Activities.
Huong, Phan Thi Thanh; Nhiem, Nguyen Xuan; Park, SeonJu; Seo, Yohan; Jeong, Sung Baek; Trang, Do Thi; Yen, Duong Thi Hai; Dung, Duong Thi; Hoa, Truong Thi Viet; Huyen, Le Thi; Lam, Le Doan Tung; Tai, Bui Huu; Kiem, Phan Van.
Affiliation
  • Huong PTT; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Nhiem NX; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Park S; Chuncheon Center, Korea Basic Science Institute (KBSI), Gib-Hyun-Kwan, 1 Kangwondaehak-gil, Chuncheon-si, Gangwon-do, 24341, Korea.
  • Seo Y; New Drug Development Center, Daegu Gyeongbuk Medical Innovation Foundation, Daegu, 41061, Korea.
  • Jeong SB; New Drug Development Center, Daegu Gyeongbuk Medical Innovation Foundation, Daegu, 41061, Korea.
  • Trang DT; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Yen DTH; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Dung DT; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Hoa TTV; VNU University of Science, Vietnam National University, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam.
  • Huyen LT; VNU University of Science, Vietnam National University, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam.
  • Lam LDT; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Tai BH; Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
  • Kiem PV; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet, Cau Giay, Hanoi, 10072, Vietnam.
Chem Biodivers ; 20(11): e202301296, 2023 Nov.
Article in En | MEDLINE | ID: mdl-37842907
Vitex 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).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vitex / Anti-Infective Agents / Antineoplastic Agents Limits: Humans Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2023 Type: Article Affiliation country: Vietnam

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vitex / Anti-Infective Agents / Antineoplastic Agents Limits: Humans Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2023 Type: Article Affiliation country: Vietnam