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Identification Of Potential Cytotoxic Inhibitors From Physalis Minima.
Le Canh, Viet Cuong; Le Ba, Vinh; Thi Hai Yen, Pham; Le Thi, Lien; Thi Thuy Hoai, Pham; Huu Dat, Ton That; Thao, Do Thi; Bach, Long Giang; Kim, Young Ho; Tuan Anh, Hoang Le.
Afiliação
  • Le Canh VC; Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang street, Hue city Vietnam.
  • Le Ba V; Institute of Marine Biochemistry, VAST, 18 Hoang Quoc Viet street, Hanoi city, Vietnam.
  • Thi Hai Yen P; College of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.
  • Le Thi L; Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang street, Hue city Vietnam.
  • Thi Thuy Hoai P; Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet street, Hanoi city, Vietnam.
  • Huu Dat TT; Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang street, Hue city Vietnam.
  • Thao DT; Graduate University of Science and Technology, VAST, 18 Hoang Quoc Viet street, Hanoi city, Vietnam.
  • Bach LG; Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang street, Hue city Vietnam.
  • Kim YH; Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang street, Hue city Vietnam.
  • Tuan Anh HL; Institute of Biotechnology, VAST, 18 Hoang Quoc Viet street, Hanoi city, Vietnam.
Nat Prod Res ; 35(12): 2082-2085, 2021 Jun.
Article em En | MEDLINE | ID: mdl-31402707
A phytochemical investigation of Physalis minima led to the isolation of six withanolides, including withanolide E (1), withaperuvin C (2), 4ß-hydroxywithanolide E (3), 28-hydroxywithaperuvin C (4), physaperuvin G (5), and 4-deoxywithaperuvin (6). Their chemical structures were elucidated by 1 D-NMR and 2 D-NMR data, as well as comparison with the data reported in the literature. All isolated compounds were evaluated for their cytotoxic activity against HepG2, SK-LU-1, and MCF7 cancer cell lines. As the obtained results, compounds 1 and 3 displayed the strongest cytotoxicity against HepG2, SK-LU-1, and MCF7 cell lines with IC50 value ranging from 0.051 ± 0.004 to 0.86 ± 0.09 µg/mL.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Physalis / Vitanolídeos / Antineoplásicos Fitogênicos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Nat Prod Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Physalis / Vitanolídeos / Antineoplásicos Fitogênicos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Nat Prod Res Ano de publicação: 2021 Tipo de documento: Article