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Antiproliferative ent-kaurane diterpenoids isolated from the roots of Zea mays L.
Wang, Andong; Fan, Yanhua; Ouyang, Qing; Fan, Chengcheng; Lin, Bin; Liu, Jianyu; Xu, Yongnan.
Afiliación
  • Wang A; School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Fan Y; State Key Laboratory for Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, China.
  • Ouyang Q; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Fan C; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Lin B; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China.
  • Liu J; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China. Electronic address: burningice@126.com.
  • Xu Y; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang 110016, China. Electronic address: ynxu@syphu.edu.cn.
Fitoterapia ; 134: 44-49, 2019 Apr.
Article en En | MEDLINE | ID: mdl-30763719
ABSTRACT
Four new ent-kaurane diterpenoid maizediterpenes A-D (1-4), along with fourteen known compounds were isolated from the roots of Zea mays (maize). Compounds 7, 15, 16 were isolated from this genus for the first time. The planar structures of the new compounds were determined by extensive analysis of their NMR and HR-ESI-MS spectra, and the absolute configurations were established on the basis of specific rotation in association with calculated ECD spectra. Compounds 2, 6 and 18 showed significant antiproliferative effects against five human cancer cell lines (A549, MDA-MB-231, SK-Hep-1, SNU638, HCT116) with IC50 values ranging from 1.99 ±â€¯0.41 µM to 15.18 ±â€¯1.17 µM.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Zea mays / Diterpenos de Tipo Kaurano / Antineoplásicos Fitogénicos Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Fitoterapia Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Zea mays / Diterpenos de Tipo Kaurano / Antineoplásicos Fitogénicos Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Fitoterapia Año: 2019 Tipo del documento: Article País de afiliación: China
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