NATURAL PRODUCT RESEARCH AND DEVELOPMENT ›› 2019, Vol. 31 ›› Issue (1): 75-80. doi: 10.16333/j.1001-6880.2019.1.012

• Article • Previous Articles     Next Articles

Chemical constituents from Cycas revoluta

ZHANG Xiu-qiong1,2,3,GENG Chang-an1,2,CHEN Xing-long1,2,LI Tian-ze1,2,ZHANG Xue-mei1,2,CHEN Ji-jun1,2,3*   

  1. 1State Key Laboratory of Phytochemistry and Plant Resources in West China,Kunming institute of Botany,Chinese Academy of Sciences,Kunming,650201;2Yunnan Key Laboratory of Natural Medicinal Chemistry,Kunming,650201,China; 3University of Chinese Academy of Science,Beijing 100049,China
  • Online:2019-01-28 Published:2019-01-28

Abstract: Sixteen compounds were isolated from the stems of Cycas revoluta by various column chromatography involving silica gel,Al2O3,and Sephadex LH-20.Their structures were identified as 5,6-dehydrosugiol (1),cunningine A (2),6-hydroxy-5,6-dehydrosugiol (3),6α-hydroxy-7-oxoferruginol (4),ligballinol (5),xanthoxyol (6),callislignan A (7),(2R,3R)-bis[(4-hydroxy-3-methoxyphenyl)methyl]-1,4-diacetate (8),secoisolariciresinol (9),dihydrokaempferol (10),4′-methylluteolin (11),5-methoxypinosylvin (12),N-benzoylphenyl alaninol (13),(E,4R)-4-hydroxy-4,5,5-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enone (14),3-hydroxy-5α,6α-epoxy-β-ionone (15),and acuminantin (16) based on HR-ESI-MS,1H,and 13C NMR spectroscopic data.All the isolates were obtained from this genus for the first time,of which compounds 13 and 16 were firstly reported as the natural products.This is the first time to reveal abietane-type diterpenes (1-4) and stilbene (12) in this genus.Compound 11 showed moderate α-glucosidase inhibitory activity in vitro,with an inhibition rate of 52.51±2.63 % at the concentration of 198.00 μg/mL.

Key words: Cycas revoluta, chemical constituents, abietane-type diterpenes, stilbenes, α-glucosidase

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