Your browser doesn't support javascript.
loading
Meroterpenoids and a naphthoquinone from Arnebia euchroma and their cytotoxic activity.
Wang, Lun; Li, Fu; Liu, Xin; Chen, Bin; Yu, Kai; Wang, Ming-Kui.
  • Wang L; Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization & Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, People's Republic of China.
  • Li F; Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization & Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, People's Republic of China.
  • Liu X; Beijing Entry-Exit Inspection and Quarantine Bureau, Beijing, People's Republic of China.
  • Chen B; Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization & Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, People's Republic of China.
  • Yu K; School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, People's Republic of China.
  • Wang MK; Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization & Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, People's Republic of China.
Planta Med ; 81(4): 320-6, 2015 Mar.
Article en En | MEDLINE | ID: mdl-25760383
ABSTRACT
Four new meroterpenoids, arnebinols A-D (1-4), and one new prenylated naphthoquinone, 5,8-O-dimethyl-11-deoxyalkannin (5), together with seven known meroterpenoids (6-12) were isolated from the roots of Arnebia euchroma. The structures of the isolated compounds were elucidated unambiguously by spectroscopic data analysis, as well as X-ray-single crystal diffraction analysis. Arnebinol A (1) and B (2) are rare meroterpenoids possessing a 6/10/5 tricyclic ring system. Compounds 1-12 were evaluated for their cytotoxicities against MG-63 and SNU387 human cancer cell lines. Compound 5 exhibited the most potent activity with IC50 values of 2.69 µM and 6.08 µM, respectively.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Boraginaceae / Monoterpenos / Fitoterapia / Neoplasias / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Boraginaceae / Monoterpenos / Fitoterapia / Neoplasias / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article