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Four new tetracyclic alkaloids with cis-decahydroquinoline motif from Myrioneuron effusum.
Zhang, Jia-Hui; Guo, Jing-Jing; Yuan, Yu-Xi; Fu, Yan-Hui; Gu, Yu-Cheng; Zhang, Yu; Chen, Duo-Zhi; Li, Shun-Lin; Di, Ying-Tong; Hao, Xiao-Jiang.
Afiliação
  • Zhang JH; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.
  • Guo JJ; Yunnan University of TCM, Kunming 650500, Yunnan, PR China.
  • Yuan YX; Yunnan University of TCM, Kunming 650500, Yunnan, PR China.
  • Fu YH; Hainan normal University, Haikou 571158, Hainan, PR China.
  • Gu YC; Syngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, UK.
  • Zhang Y; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China.
  • Chen DZ; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China.
  • Li SL; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China.
  • Di YT; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China. Electronic address: diyt@mail.kib.ac.cn.
  • Hao XJ; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, PR China. Electronic address: haoxj@mail.kib.ac.cn.
Fitoterapia ; 112: 217-21, 2016 Jul.
Article em En | MEDLINE | ID: mdl-27316979
ABSTRACT
Four new Myrioneuron alkaloids, mysumamides A-D (1-4), along with three known ones were isolated from the twigs and leaves of Myrioneuron effusum. All of these alkaloids possessed the tetracyclic skeleton and contained the decahydroquinoline (cis-DHQ) moiety. Their structures and relative configurations were elucidated on the basis of spectroscopic methods, especially 2D NMR techniques. The absolute configuration of 1 was determined by single-crystal X-ray diffraction. The cytotoxic activities of these compounds were also evaluated in vitro.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolinas / Rubiaceae / Alcaloides Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolinas / Rubiaceae / Alcaloides Idioma: En Ano de publicação: 2016 Tipo de documento: Article