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Cytotoxic constituents from Isotrema tadungense.
Truong, Luu Hong; Cuong, Nguyen Hieu; Dang, Tran Huu; Hanh, Nguyen Thi My; Thi, Vien Le; Tran Thi Hong, Hanh; Nguyen, Hai Dang; Nguyen Xuan, Cuong; Nguyen Hoai, Nam; Minh, Chau Van.
Afiliação
  • Truong LH; Southern Institute of Ecology, Vietnam Academy of Science and Technology (VAST), Ho Chi Minh City 71515, Vietnam.
  • Cuong NH; Southern Institute of Ecology, Vietnam Academy of Science and Technology (VAST), Ho Chi Minh City 71515, Vietnam.
  • Dang TH; Southern Institute of Ecology, Vietnam Academy of Science and Technology (VAST), Ho Chi Minh City 71515, Vietnam.
  • Hanh NTM; Southern Institute of Ecology, Vietnam Academy of Science and Technology (VAST), Ho Chi Minh City 71515, Vietnam.
  • Thi VL; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Tran Thi Hong H; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Tran Hong Quang; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Nguyen HD; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Nguyen Xuan C; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Nguyen Hoai N; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
  • Minh CV; Institute of Marine Biochemistry, Vietnam Academy of Science and Technology (VAST), Hanoi 10072, Vietnam.
J Asian Nat Prod Res ; 23(5): 491-497, 2021 May.
Article em En | MEDLINE | ID: mdl-32212861
ABSTRACT
In our search for cytotoxic constituents from Vietnamese plants, the methanolic extract of Isotrema tadungense was found to exhibit significant cytotoxic effect. Subsequent phytochemical investigation of ethyl acetate fractions of this plant led to isolation of 11 compounds including one new arylbenzofuran rhamnoside namely aristolochiaside (1), two aristololactams (2 and 3), three lignanamides (4-6) and five phenolic amides (7-11). Their structures were elucidated by 1 D and 2 D NMR and HR-QTOF-MS experiments. Among the isolated compounds, aristolochiaside (1), aristolactam AIIIa (2) and N-trans-sinapoyltyramine (10) exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 7.59 ± 1.03, 8.51 ± 1.73 and 9.77 ± 1.25 µM, respectively.[Formula see text].
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antineoplásicos Limite: Humans Idioma: En Revista: J Asian Nat Prod Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antineoplásicos Limite: Humans Idioma: En Revista: J Asian Nat Prod Res Ano de publicação: 2021 Tipo de documento: Article