[1] 刘颖,郭明晔,白根本. 绿原酸的研究进展[J]. 中药材, 2012,35(7): 1180–1185.
[2] 席利莎,木泰华,孙红男. 绿原酸类物质的国内外研究进展[J]. 核农学报, 2014,28(2): 292–301.
[3] Xu J G, Hu Q P, Liu Y. Antioxidant and DNA-Protective activities of chlorogenic acid isomers[J]. Journal of Agriculture and Food Chemistry, 2012,60: 11625–11630.
[4] 曾沧江. 中国冬青科植物志资料[J]. 植物研究, 1981,1(1–2): 1–44.
[5] 俸宇星,陈书坤,赵瑞峰,梁畴芬. 中国冬青属苦丁茶名实辨证[J]. 植物分类学报, 1998,36(4): 353–358.
[6] 中国科学院中国植物志编辑委员会. 中国植物志(第45卷第2册)[M]. 北京: 科学出版社, 1999: 1–226.
[7] Wu Z Y, Raven P H, Hong D Y. Flora of China (Vol.11)[M]. Beijing: Science Press &St. Louis: Missouri Botanical Garden Press, 2008: 359–438.
[8] 王新,陆慧宁,林少琨. 苦丁茶冬青叶化学成分及药理作用研究进展[J]. 天然产物研究与开发, 2005,17(3): 366—370.
[9] 刘瑾,丁平. 冬青属药用植物资源、化学成分及药理作用研究进展[J]. 广州中医药大学学报, 2008,25(3): 277–280.
[10] Phuong T T, Nguyen D S, Tran M N, Tran M H, Nguyen H D, Nguyen D T, KiHwan B, Won K O. Antioxidant activity and principles of Vietnam bitter tea Ilex kudingcha[J]. Food Chemistry, 2009,113(1): 139–145.
[11] Song C W, Xie C, Zhou Z W, Yu S G, Fang N B. Antidiabetic effect of an active components group from Ilex kudingcha and its chemical composition[J]. Evidence-Based Complementary and Alternative Medicine, 2012: 1–12.
[12] Song J L, Qian Y, Li G J, Zhao X. Anti-inflammatory effects of kudingcha methanol extract (Ilex kudingcha C.J. Tseng) in dextran sulfate sodium–induced ulcerative colitis[J]. Molecular Medicine Reports, 2013,8(4): 1256–1262.
[13] Zhu S L, Wei L Y, Lin G X. Metabolic alterations induced by Kudingcha lead to cancer cell apoptosis and metastasis inhibition[J]. Nutrition and Cancer, 2020,72(4): 696–707.
[14] Xie M H, Chen G J, Hu B, Zhou L, Ou S Y, Zeng X X, Sun Y. Hydrolysis of dicaffeoylquinic acids from Ilex kudingcha happens in the colon by intestinal microbiota[J]. Journal of Agriculture and Food Chemistry, 2016,64(51): 9624?9630.
[15] Negishi O, Negishi Y, Yamaguchi F, Sugahara T. Deodorization with Kudingcha containing a large amount of caffeoyl quinic acid derivatives[J]. Journal of Agriculture and Food Chemistry, 2004,52(17): 5513?5518.
[16] Markovic S, Tosovic J. Comparative study of the antioxidative activities of caffeoylquinic and caffeic acids[J]. Food Chemistry, 2016,210: 585–592.
[17] Xu D L, Wang Q C, Zhang W Q, Hu B, Zhou L, Zeng X X, Sun Y. Inhibitory activities of caffeoylquinic acid derivatives from Ilex kudingcha C.J. Tseng on α-glucosidase from Saccharomyces cerevisiae[J]. Journal of Agricultural and Food Chemistry, 2015,63: 3694–3703.
[18] Wan P, Xie M H, Chen G J, Dai Z Q,Hu B, Zeng X X, Sun Y. Anti-inflammatory effects of dicaffeoylquinic acids from Ilex kudingcha on lipopolysaccharide-treated RAW264.7 macrophages and potential mechanisms[J]. Food and Chemical Toxicology, 2019,126: 332–342.
[19] Wan P, Peng Y J, Chen G J, Xie M H, Dai Z Q, Huang K Y, Wei D, Zeng X X, Sun Y. Dicaffeoylquinic acids from Ilex kudingcha attenuate dextran sulfate sodium induced colitis in C57BL/6 mice in association with the modulation of gut microbiota[J]. Journal of Functional Foods, 2019,61: 1–13.
[20] Bajko E, Kalinowska M, Borowski P, Siergiejczyk L, Lewandowski W. 5-O-Caffeoylquinic acid: a spectroscopic study andbiological screening for antimicrobial activity[J]. LWT-Food Science and Technology, 2016,65: 471–479.
[21] 王明彦. 苦丁茶中二咖啡酰奎宁酸对人肿瘤细胞的体外抑制作用及其机制研究[D]. 武汉: 湖北中医药大学硕士学位论文, 2014.
[22] Robinson W E, Reinecke M G, Abdel-Malek S, Chow S A. Inhibitors of HIV-1 replication that inhibit HIV intergrase[J]. Proceedings of the National Academy of the Sciences of USA, 1996,93(13): 6323–6331.
[23] 李玉山. 绿原酸在天然植物中的分布和提取纯化工艺研究进展[J]. 解放军药学学报, 2012,28: 355–359.
[24] Trugo L C, Macrae R. A study of the effect of roasting on the chlorogenic acid composition of coffee using HPLC[J]. Food Chemistry, 1984,15(3): 219–227.
[25] Dawidowicz A L, Typek R. Thermal Stability of 5-o-caffeoylquinic acid in aqueous solutions at different heating conditions[J]. Journal of Agricultural and Food Chemistry, 2010,58(24): 12578–12584.
[26] Dawidowicz A L, Typek R. Thermal transformation of trans-5-O-caffeoylquinic acid (trans–5-CQA) in alcoholic solutions[J]. Food Chemistry, 2015,167: 52–60.
[27] Raheem K S, Botting N P, Williamson G, Barron D. Total synthesis of 3,5-O-dicaffeoylquinic acid and its derivatives[J]. Tetrahedron Letters, 2011,52(52): 7175–7177. |