天然产物研究与开发 ›› 2020, Vol. 32 ›› Issue (4): 613-621.doi: 10.16333/j.1001-6880.2020.4.010

• 研究简报 • 上一篇    下一篇

缅甸产青紫葛的化学成分及细胞毒活性研究

张东东1,2,3,李兴玉4,刘珮4,崔大鹏4,王跃虎2,3*,杨雪飞1,2,3*


  

  1. 1中国科学院东南亚生物多样性研究中心,耶津 05282;2中国科学院昆明植物研究所资源植物与生物技术重点实验室;3中国科学院昆明植物研究所云南野生资源植物研发重点实验室;4云南农业大学,昆明 650201

  • 出版日期:2020-04-28 发布日期:2020-06-05
  • 基金资助:
    生态环境部生物多样性调查评估项目(2019HJ2096001006);中国科学院东南亚生物多样性研究中心(Y4ZK111B01);中国科学院国际合作局对外合作重点项目(153631KYSB20160004);国家自然科学基金(31670338) 

 Chemical constituents and cytotoxic activities of Cissus javana from Myanmar

ZHANG Dong-dong1,2,3,LI Xing-yu4,LIU Pei4,CUI Da-peng4,WANG Yue-hu2, 3*,YANG Xue-fei1,2,3*   

  1. 1Southeast Asia Biodiversity Research Institutes,Chinese Academy of Sciences,Yezin 05282,Myanmar; 2 Key Laboratory of Economic Plants and Biotechnology,Kunming Institute of Botany,Chinese Academy of Sciences;3Yunnan Key Laboratory for Wild Plant Resource,Kunming Institute of Botany,Chinese Academy of Sciences;4 Yunnan Agricultural University,Kunming,650201,China

  • Online:2020-04-28 Published:2020-06-05

摘要: 对缅甸传统上用于抗肿瘤的葡萄科药用植物,青紫葛的块根进行化学成分研究和细胞毒活性评价。采用色谱技术从青紫葛块根乙醇提取物中分离到了19个化合物。基于波谱数据将这19个化合物分别鉴定为2-C-β-D-吡喃葡萄糖基-3,5-二羟基-4-甲氧基苯甲酸(1)、picraquassioside D(2)、2-O-β-D-吡喃葡萄糖基氧基-4,6-二羟基异丁基苯基酮(3)、岩白菜素(4)、(-)-蛇葡萄素A(5)、(-)-表儿茶素(6)、(-)-表阿夫儿茶精(7)、(E)-白藜芦醇(8)、4-O-(2-羟基-1-羟甲基乙基)-二氢松柏醇(9)、25-过氧羟基环阿尔廷-23-烯-3β-醇(10)、羽扇豆醇(11)、δ-香树精(12)、palmarumycin SA1(13)、(3R)-palmarumycin BG1(14)、(6R,9S)-roseoside(15)、(-)-南烛木树脂酚-2a-O-β-D-吡喃葡萄糖苷(16)、(-)-南烛木树脂酚-3a-O-β--D-吡喃葡萄糖苷(17)、(+)-异落叶松脂素-3a-O-β-D-吡喃葡萄糖苷(18)以及(+)-南烛木树脂酚-3a-O-β-D-吡喃葡萄糖苷(19)。其中化合物1~4、13和14为酚类,5和8为二苯乙烯类,6和7为黄烷醇,9为苯丙素,10~12为三萜类,15是倍半萜糖苷,16~19为木脂素糖苷。化合物1~3、5~7、9、10、13~19是从该属植物中首次分离得到。青紫葛块根乙醇提取物对人结肠癌SW480细胞株具有较好的抑制活性,IC50值为15.12 μg/mL。化合物10对人白血病HL-60细胞株和人结肠癌SW480细胞株均具有较好的抑制活性,IC50值分别为12.97±0.69和21.08±0.70 μM。研究首次对青紫葛块根的化学成分进行报道,并初步验证了缅甸传统医药体系中将其用作抗肿瘤药物的合理性。


关键词: 葡萄科, 青紫葛, 传统药物, 三萜, 细胞毒活性

Abstract:

The chemical constituents and cytotoxic activities of roots of Cissus javana (Vitaceae),a medicinal plant used to treat tumors in Myanmar traditional system,were studied.Nineteen compounds were isolated by chromatographic techniques and elucidated based on spectroscopic data and comparison with reported data from ethanolic extract.These compounds were identified as 2-C-β-D-glucopyranosyl-3,5-dihydroxy-4-methoxy-benzoic acid (1),picraquassioside D (2),2-O-β-D-glucopyranosyloxy-4,6-dihydroxyisovalerophenone (3),bergenin (4),(-)-ampelopsin A (5),(-)-epicatechin (6),(-)-epiafzelechin (7),(E)-resveratrol (8),4-O-(2-hydroxy-1-hydroxymethylethyl)-dihydroconiferyl alcohol (9),25-hydroperoxycycloart-23-en-3β-ol (10),lupeol (11),δ-amyrin (12),palmarumycin SA1 (13),(3R)-palmarumycin BG1 (14),(6R,9S)-roseoside (15),(-)-lyoniresinol-2a-O-β-D-glucopyranoside (16),(-)-lyoniresinol-3a-O-β-D-glucopyranoside (17),(+)-isolarisiresinol-3a-O-β-D-glucopyranoside (18),and (+)-lyoniresinol-3a-O-β-D-glucopyranoside (19),respectively.Compounds 1-4,13,and 14 are phenols;5 and 8 are stilbenes;6 and 7 are flavanols;9 is a phenylpropanoid,10-12 are triterpenoids;15 is a sesquiterpenoid glucoside;16-19 are lignan glucosides.Compounds 1-3,5-7,9,10,and 13-19 were isolated from Cissus genus for the first time.The ethanolic extract of Cissus javana roots showed good cytotoxic activity against human rectal cancer SW480 cell line with an IC50 value of 15.12 μg/mL.Compound 10 showed potent cytotoxic activities against human leukemia HL-60 cell line and human rectal cancer SW480 cell line,with IC50 values of 12.97±0.69 and 21.08±0.70 μM,respectively.This research reported the chemical constitutes of C. javana roots for the first time;it provided evidence for cytotoxic activities of C. javana,which comply with the traditional use for antitumor in Myanmar.

Key words: Vitaceae, Cissus javana, traditional medicine, triterpenoids, cytotoxic activity

中图分类号:  R284.2