Your browser doesn't support javascript.
loading
A sesquiterpenoid tropolone and 1,2,3,4-tetrahydronaphthalene derivatives from Olax imbricata roots.
Nguyen, Huong T M; Vo, Nga T; Huynh, Suong T M; Do, Lien T M; Aree, Thammarat; Tip-Pyang, Santi; Phan, Cam-Tu D; Trung, Nguyen T; Nguyen, Phung K P.
Afiliação
  • Nguyen HTM; University of Science, National University-Ho Chi Minh City, Ho Chi Minh City 748355, Viet Nam.
  • Vo NT; Ho Chi Minh City University of Technology and Education, Ho Chi Minh City 720214, Viet Nam.
  • Huynh STM; University of Natural Resources and Environment Ho Chi Minh City, Ho Chi Minh City 736400, Viet Nam.
  • Do LTM; Institute of Environmental-Energy Technology, Sai Gon University, Ho Chi Minh City 748355, Viet Nam.
  • Aree T; Center of Excellence in Natural Products Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Phayathai Road, Patumwan, Bangkok 10330, Thailand.
  • Tip-Pyang S; Center of Excellence in Natural Products Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Phayathai Road, Patumwan, Bangkok 10330, Thailand.
  • Phan CD; Department of Chemistry, and Laboratory of Computational Chemistry and Modelling, Quy Nhon University, 55100, Viet Nam.
  • Trung NT; Department of Chemistry, and Laboratory of Computational Chemistry and Modelling, Quy Nhon University, 55100, Viet Nam.
  • Nguyen PKP; University of Science, National University-Ho Chi Minh City, Ho Chi Minh City 748355, Viet Nam. Electronic address: kimphiphung@yahoo.fr.
Fitoterapia ; 132: 1-6, 2019 Jan.
Article em En | MEDLINE | ID: mdl-30439445
The methanol extract of Olax imbricata roots afforded one new sesquiterpenoid tropolone and three new 1,2,3,4-tetrahydronaphthalene derivatives, olaximbrisides A-D (1-4). Their structures were determined by 1D and 2D NMR experiments in combination of HRESIMS. The relative configurations were assigned by the NOESY experiments. The absolute configurations were established by a combination of X-ray diffraction analysis and electronic circular dichroism (ECD) experiments. All isolated compounds were evaluated for their cytotoxic effects against some cancer cell lines. Among them, compound 1 exhibited the cytotoxicities against MCF-7, HepG2 and LU cell lines with IC50 values of 16.3, 34.3 and 8.0 µM, respectively.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tetra-Hidronaftalenos / Tropolona / Olacaceae / Antineoplásicos Fitogênicos Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Fitoterapia Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tetra-Hidronaftalenos / Tropolona / Olacaceae / Antineoplásicos Fitogênicos Limite: Humans País/Região como assunto: Asia Idioma: En Revista: Fitoterapia Ano de publicação: 2019 Tipo de documento: Article