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Sesquiterpenes and diterpenes with cytotoxic activities from the aerial parts of Carpesium humile.
Xu, Dong-Dong; Yan, Yuan; Jiang, Chun-Xiao; Liang, Jing-Jing; Li, Hong-Fang; Wu, Quan-Xiang; Zhu, Ying.
Afiliación
  • Xu DD; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China.
  • Yan Y; Department of Physiology, College of Basic Medicine, Lanzhou University, Lanzhou 730000, PR China; Key Laboratory of Pre-clinical Study for New Drugs of Gansu Province, Lanzhou 730000, PR China.
  • Jiang CX; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China.
  • Liang JJ; Department of Physiology, College of Basic Medicine, Lanzhou University, Lanzhou 730000, PR China; Key Laboratory of Pre-clinical Study for New Drugs of Gansu Province, Lanzhou 730000, PR China.
  • Li HF; Department of Physiology, College of Basic Medicine, Lanzhou University, Lanzhou 730000, PR China; Key Laboratory of Pre-clinical Study for New Drugs of Gansu Province, Lanzhou 730000, PR China.
  • Wu QX; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China.
  • Zhu Y; State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, PR China. Electronic address: zhuy@lzu.edu.cn.
Fitoterapia ; 128: 50-56, 2018 Jul.
Article en En | MEDLINE | ID: mdl-29689329
ABSTRACT
Carpesium humile Winkl is an endemic Chinese species and no previous phytochemical studies have been reported for this species. Two new germacranolides (1 and 2) and a new phytane diterpene (5), together with five known compounds (two sesquiterpenoids and three diterpenoids), were isolated from the aerial parts of C. humile. Their structures were elucidated on the basis of extensive spectroscopic analysis. The conformations and absolute configurations of 1 and 2 were established by combinative analysis of NMR, CD exciton chirality, and X-ray crystallography data. Four germacranolides (1-4) showed strong cytotoxic activities, with broad spectrum activities against six human cancer (HepG2, HeLa, HL60, SGC7901, Lewis, and MDA231) cell lines in vitro using MTT assay, with IC50 values from 3.09 to 7.71 µg/mL. Diterpenes (5, 6, and 8) also displayed good cytotoxic activities for selected cancer cell lines, with IC50 values in the range 5.46-8.08 µg/mL.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Asteraceae / Sesquiterpenos de Germacrano / Diterpenos / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Revista: Fitoterapia Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Asteraceae / Sesquiterpenos de Germacrano / Diterpenos / Antineoplásicos Fitogénicos Límite: Humans Idioma: En Revista: Fitoterapia Año: 2018 Tipo del documento: Article
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