[1]
|
Takaoka, M. (1940) The Phenolic Substances of White Helleboro (Veratrum Grandiflorum Hoes. Fil.). III. Nippon Kagaku Kaishi, 61, 30-34. https://doi.org/10.1246/nikkashi1921.61.30
|
[2]
|
夏曦, 徐嘉琪, 胡越高, 陈煜, 杨鸿均, 赵志刚. 白藜芦醇的合成研究进展[J]. 化学试剂, 2019, 41(9): 873-881.
|
[3]
|
Huang, H., Liu, R.N. and Ou, W.H. (2020) A Mini Review on Chemical Synthesis of Resveratrol. Mini-Reviews in Organic Chemistry, 17, 546-558. https://doi.org/10.2174/1570193X16666190617155558
|
[4]
|
Song, J.T., Woo, D.U., Lee, Y.J., et al. (2021) The Semi-Supervised Strategy of Machine Learning on the Gene Family Diversity to Unravel Resveratrol Synthesis. Plants, 10, Article No. 2058. https://doi.org/10.3390/plants10102058
|
[5]
|
Borys, S., Khozmi, B., Kranc, W., et al. (2017) Resveratrol and Its Analogues—Is It a New Strategy of Anticancer Therapy? Advances in Cell Biology, 5, 32-42. https://doi.org/10.1515/acb-2017-0003
|
[6]
|
Kumar, S., Chang, Y.C., Lai, K.H. and Hwang, T.L. (2021) Resveratrol, a Molecule with Anti-Inflammatory and Anti-Cancer Activities: Natural Product to Chemical Synthesis. Current Medicinal Chemistry, 28, 3773-3786.
https://doi.org/10.2174/0929867327999200918100746
|
[7]
|
Shu, L.Y., Hou, X.Y., Song, G.Y., et al. (2021) Comparative Analysis of Long Non Coding RNA Expression Profiles Induced by Resveratrol and Metformin Treatment for Hepatic Insulin Resistance. International Journal of Molecular Medicine, 48, Article No. 206. https://doi.org/10.3892/ijmm.2021.5039
|
[8]
|
Nam, K.Y., Damodar, K., Lee, Y., et al. (2021) Design and Synthesis of π-Extended Resveratrol Analogues and in Vitro Antioxidant and Anti-Inflammatory Activity Evaluation. Molecules, 26, Article No. 646.
https://doi.org/10.3390/molecules26030646
|
[9]
|
Torregrosa-Muñumer, R., Vara, E., Fernández‑Tresguerres, J.A. and Gredilla, R. (2021) Resveratrol Supplementation at Old Age Reverts Changes Associated with Aging in Inflammatory, Oxidative and Apoptotic Markers in Rat Heart. European Journal of Nutrition, 60, 2683-2693. https://doi.org/10.1007/s00394-020-02457-0
|
[10]
|
刘少静. 新型糖苷化反应研究[D]: [硕士学位论文]. 青岛: 中国海洋大学, 2013.
|
[11]
|
梁娟. 新型氧糖苷类化合物的合成研究[D]: [硕士学位论文]. 广州: 广东药科大学, 2017.
|
[12]
|
Danishefsky, S.J. and Allen, J.R. (2000) From the Laboratory to the Clinic: A Retrospective on Fully Synthetic Carbohydrate-Based Anticancer Vaccines. Angewandte Chemie International Edition, 31, 836-863.
https://doi.org/10.1002/(SICI)1521-3773(20000303)39:5%3C836::AID-ANIE836%3E3.0.CO;2-I
|
[13]
|
Meng, S.S., Wang, Q., Huang, G.B., et al. (2018) B(C6F5)3 Catalyzed Direct Nucleophilic Substitution of Benzylic Alcohols: an Effective Method of Constructing C-O, C-S and C-C Bonds from Benzylic Alcohols. RSC Advances, 8, 30946-30949. https://doi.org/10.1039/C8RA05811C
|
[14]
|
Kolb, H.C., Finn, M.G. and Sharpless, K.B. (2001) Click Chemistry: Diverse Chemical Function from a Few Good Reactions. Angewandte Chemie International Edition, 40, 2004-2021.
https://doi.org/10.1002/1521-3773(20010601)40:11%3C2004::AID-ANIE2004%3E3.0.CO;2-5
|
[15]
|
Balmond, E.I., Coe, D.M., Galan, M.C., et al. (2012) α-Selective Organocatalytic Synthesis of 2-Deoxygalactosides. Angewandte Chemie International Edition, 124, 9286-9289. https://doi.org/10.1002/ange.201204505
|
[16]
|
蔡孟深, 邱东旭. 芳香碳苷的高选择性合成[J]. 科学通报, 1989(17): 1339-1341.
|
[17]
|
Helferich, B. and Schmitz-Hillebrecht, E. (1933) A New Method for the Synthesis of Glycosides of Phenols. Chemische Berichte, 66, 378-383.
|
[18]
|
于建新, 伊向艺, 刘方明, 刘育亭. 1-芳酰基-4-(1’-N-β-D-吡喃型糖基)氨基硫脲类化合物的合成(英文) [J]. 合成化学, 2000(2): 137-141.
|
[19]
|
Kochetkov, N.K., Bochkov, A.F., Sokolavskaya, T.A., et al. (1971) Modifications of the Orthoester Method of Glycosylation. Carbohydrate Research, 16, 17-27. https://doi.org/10.1016/S0008-6215(00)86094-2
|
[20]
|
Demetzos, C., Skaltsounis, A.L., Tillequin, F. and Koch, M. (1990) Phase-Transfer-Catalyzed Synthesis of Flavonoid Glycosides. Planta Medica, 56, 535. https://doi.org/10.1055/s-2006-961099
|
[21]
|
Friesen, R.W. and Danishefsky, S.J. (1989) On the Controlled Oxidative Coupling of Glycals: A New Strategy for the Rapid Assembly of Oligosaccharides. ChemInform, 20, No. 49. https://doi.org/10.1002/chin.198949283
|
[22]
|
苏丹. 白藜芦醇与白藜芦醇苷的药效学与药代动力学研究[D]: [硕士学位论文]. 西安: 第四军医大学, 2010.
|
[23]
|
Xiong, D., Lu, S., Wu, J., et al. (2017) Improving Key Enzyme Activity in Phenylpropanoid Pathway with a Designed Biosensor. Metabolic Engineering, 40, 115-123. https://doi.org/10.1016/j.ymben.2017.01.006
|
[24]
|
Gachon, C., Langlois-Meurinne, M. and Saindrenan, P. (2005) Plant Secondary Metabolism Glycosyltransferases: The Emerging Functional Analysis. Trends in Plant Science, 10, 542-549. https://doi.org/10.1016/j.tplants.2005.09.007
|
[25]
|
郝旭晨, 董燕婕, 范丽霞, 苑学霞, 梁京芸, 王磊, 李大鹏, 赵善仓. 花生中白藜芦醇和白藜芦醇苷的提取及含量测定[J]. 中国食物与营养, 2020, 26(3): 27-30.
|
[26]
|
Ioannou, I., Barboza, E., Willig, G., et al. (2021) Implementation of an Enzyme Membrane Reactor to Intensify the α-O-Glycosylation of Resveratrol Using Cyclodextrins. Pharmaceuticals, 14, Article No. 319.
https://doi.org/10.3390/ph14040319
|
[27]
|
郑哲彬, 赵守训, 邓京振, 等. 藜芦酚碳甙的分离及鉴定[J]. 中国药科大学学报, 1995, 26(1): 5-7.
|
[28]
|
孙娟. 虎杖中白藜芦醇苷和挥发油的分离分析研究[D]: [硕士学位论文]. 长沙: 中南大学, 2007.
|
[29]
|
Wang, Y.H., Zhang, Z.K., He, H.P., et al. (2007) Stilbene C-Glucosides from Cissus repens. Journal of Asian Natural Products Research, 9, 631-636. https://doi.org/10.1080/10286020600979548
|
[30]
|
郝新才, 金明, 明东坡, 张勇洪, 谭艳. 酶解法提取虎杖中白藜芦醇苷的工艺研究[J]. 湖北医药学院学报, 2018, 37(4): 346-348.
|
[31]
|
Baderschneider, B. and Winterhalter, P. (2000) Isolation and Characterization of Novel Stilbene Derivatives from Riesling Wine. Journal of Agricultural and Food Chemistry, 48, 2681-2686. https://doi.org/10.1021/jf991348k
|
[32]
|
Brandolini, V., Maietti, A., Tedeschi, P., et al. (2002) Capillary Electrophoresis Determination, Synthesis, and Stability of Resveratrol and Related 3-O-β-d-Glucopyranosides. Journal of Agricultural & Food Chemistry, 50, 7407-7411.
|
[33]
|
Hanamura, S., Hanaya, K., Shoji, M., et al. (2016) Synthesis of Acacetin and Resveratrol 3,5-di-O-β-Glucopyranoside Using Lipase-Catalyzed Regioselective Deacetylation of Polyphenol Glycoside Peracetates as the Key Step. Journal of Molecular Catalysis B: Enzymatic, 128, 19-26. https://doi.org/10.1016/j.molcatb.2016.03.001
|
[34]
|
Trobo-Maseda, L., Orrego, A.H., Guisan, J.M., et al. (2020) Coimmobilization and Colocalization of a Glycosyltransferase and a Sucrose Synthase Greatly Improves the Recycling of UDP-Glucose: Glycosylation of Resveratrol 3-O -β-D-Glucoside. International Journal of Biological Macromolecules, 157, 510-521.
https://doi.org/10.1016/j.ijbiomac.2020.04.120
|
[35]
|
Zhang, Z.J., Yu, B. and Schmidt, R.R. (2006) Synthesis of Mono- and Di-O-β-D-Glucopyranoside Conjugates of (E)-Resveratrol. Synthesis, 2006, 1301-1306. https://doi.org/10.1055/s-2006-926394
|
[36]
|
陈鹏, 杨丽川, 雷伟亚, 等. 虎杖苷抗血栓形成作用的实验研究[J]. 昆明医学院学报, 2006, 27(1): 10-12.
|
[37]
|
None (2014) Synthesis of Glycosides of Resveratrol, Pterostilbene, and Piceatannol by Glucosyltransferase from Phytolaccaamericana Expressed in Bacillus subtilis and Their Chemopreventive Activity against Cancer, Allergic, and Alzheimer’s Diseases. Glycobiology Insights, 4, 1-6. https://doi.org/10.4137/GBI.S14123
|
[38]
|
Aguirre, L., Palacios-Ortega, S., Fernández-Quintela, A., et al. (2019) Pterostilbene Reduces Liver Steatosis and Modifies Hepatic Fatty Acid Profile in Obese Rats. Nutrients, 11, Article No. 961. https://doi.org/10.3390/nu11050961
|
[39]
|
Boccellino, M., Donniacuo, M., Bruno, F., et al. (2019) Protective Effect of Piceatannol and Bioactive Stilbene Derivatives against Hypoxia-Induced Toxicity in H9c2 Cardiomyocytes and Structural Elucidation as 5-LOX Inhibitors. European Journal of Medicinal Chemistry, 180, 637-647. https://doi.org/10.1016/j.ejmech.2019.07.033
|
[40]
|
袁慧坤, 马倩, 袁文华, 赵文文, 刘香杉, 刁新平. 地衣芽孢杆菌的研究进展[J]. 黑龙江畜牧兽医, 2019(11): 43-45.
|
[41]
|
Pandey, R.P., Parajuli, P., Shin, J.Y., et al. (2014) Enzymatic Biosynthesis of Novel Resveratrol Glucoside and Glycoside Derivatives. Applied and Environmental Microbiology, 80, 7235-7243.
https://doi.org/10.1128/AEM.02076-14
|
[42]
|
Pizzut-Serin, S., Potocki-Véronèse, G., van der Veen, B.A., et al. (2005) Characterisation of a Novel Amylosucrase from Deinococcus radiodurans. FEBS Letters, 579, 1405-1410. https://doi.org/10.1016/j.febslet.2004.12.097
|
[43]
|
王书元, 张雨彤, 杨芳, 于晓海, 陈慧, 金建明. 白藜芦醇葡萄糖苷的生物合成[J]. 食品工业, 2020, 41(3): 191-195.
|
[44]
|
Orsini, F., Pelizzoni, F., Bellini, B., et al. (1997) Synthesis of Biologically Active Polyphenolic Glycosides (Combretastatin and Resveratrol Series). Carbohydrate Research, 301, 95-109. https://doi.org/10.1016/S0008-6215(97)00087-6
|
[45]
|
Hernández-Romero, Y., Rojas, J.I., Castillo, R., et al. (2004) Spasmolytic Effects, Mode of Action, and Structure-Activity Relationships of Stilbenoids from Nidema boothii. Journal of Natural Products, 67, 160-167.
https://doi.org/10.1021/np030303h
|
[46]
|
Regev-Shoshani, G., Shoseyov, O., Bilkis, I., et al. (2003) Glycosylation of Resveratrol Protects It from Enzymicoxidation. Biochemical Journal, 374, 157-163. https://doi.org/10.1042/bj20030141
|
[47]
|
Singh, Y. and Demchenko, A.V. (2019) Koenigs-Knorr Glycosylation Reaction Catalyzed by Trimethylsilyl Trifluoromethanesulfonate. Chemistry—A European Journal, 25, 1461-1465. https://doi.org/10.1002/chem.201805527
|
[48]
|
Koenigs, W. and Knorr, E. (1901) Uebereinige Derivate des Traubenzuckers und der Galactose. Berichte der deutschen chemischen Gesellschaft, 34, 957-981. https://doi.org/10.1002/cber.190103401162
|
[49]
|
梁海晶. 新型糖苷化方法学研究[D]: [硕士学位论文]. 兰州: 兰州大学, 2020.
|
[50]
|
Schmidt, R.R. and Michel, J. (1980) Facile Synthesis of α- and β-O-GlycosylImidates; Preparation of Glycosides and Disaccharides. Angewandte Chemie International Edition in English, 19, 731-732.
https://doi.org/10.1002/anie.198007311
|
[51]
|
Schmidt, R.R. and Kinzy, W. (1994) Anomeric-Oxygen Activation for Glycoside Synthesis: The Trichloroacetimidate Method. Advances in Carbohydrate Chemistry and Biochemistry, 50, 21-123.
https://doi.org/10.1016/S0065-2318(08)60150-X
|
[52]
|
Aiguabella, N., Holland, M.C. and Gilmour, R. (2016) Fluorine-Directed 1,2-Trans Glycosylation of Rare Sugars. Organic & Biomolecular Chemistry, 14, 5534-5538. https://doi.org/10.1039/C6OB00025H
|
[53]
|
任金红, 王博, 赵冬梅, 张健, 李刚, 程卯生. 白藜芦醇苷的合成及其维甲酸代谢阻断活性研究[J]. 中国药物化学杂志, 2010, 20(1): 19-24.
|