[1] 张飞龙,李钢. 生漆的组成结构与其性能的关系研究[J]. 中国生漆,2000,19(3):31-37.
[2] 孙祥玲,吴国民,孔振武. 生漆改性及其应用进展[J]. 生物质化学工程,2014,48(2):41-47.
[3] 赵喜萍,魏朔南. 中国生漆化学成分研究[J]. 中国野生植物资源,2007,26(6):1-4.
[4] HONDA T,LU R,SAKAI R,et al. Characterization and comparison of asian lacquer saps[J]. Progress in Organic Coatings,2008,61(1):68-75.
[5] 何源峰,王成章,陆榕. HPLC-MS法表征坝漆酚类化合物的结构[J]. 林产化学与工业,2012,32(6):47-51.
[6] SUNTHANKAR S V,DAWSON C R. The structural identification of the olefinic components of Japanese lac urushiol[J]. Journal of the American Chemical Society,1954,76(20):5070-5074.
[7] YAMAUCHI Y,OSHIMA R,KUMANOTANI J. Separation of Japanese lac urushiol diacetate on silver nitrate-coated silica gel columns by high-performance liquid chromatography[J]. Journal of Chromatography A,1980,198(1):49-56.
[8] HATADA K,KITAYAMA T,NISHIURA T,et al. Structural analysis of the components of Chinese lacquer "Kuro-urushi"[J]. Macromolecular Chemistry and Physics,1994,195(5):1865-1870.
[9] LU R,YUKIO K,TETSUO M. Characterization of lipid components of Melanorrhoea usitata lacquer sap[J]. Talanta,2007,71(4):1536-1540.
[10] KIM D H,CHOI J O,YANG J S,et al. Analysis of urushiols by liquid chromatography/atmospheric pressure chemical ionization-ion trap mass spectrometry[J]. Journal of Liquid Chromatography & Related Technologies,2003,26(1):17-28.
[11] DU Y M,OSHIMA R,KUMANOTANI J. Reversed-phase liquid chromatographic separation and identification of constituents of uroshiol in the sap of the lac tree,Rhus vernicifera[J]. Journal of Chromatography A,1984,284:463-473.
[12] 林乔源,许奎钫,胡邦豪,等. 中国漆漆酚的核磁共振研究[J]. 科学通报,1983,28(5):274-276.
[13] 邱峰,李丽云,黄照庚,等. 中国生漆漆酚组分的分离及NMR研究[J]. 波谱学杂志,1987,4(4):337-343.
[14] 吴采樱,曾昭睿. 用毛细管柱分离鉴定中国生漆中漆酚的组成结构[J]. 中国生漆,1992,11(4):3-5.
[15] 李林,魏朔南,胡正海. 生漆中漆酚类化合物的HPLC-ESI-MS分析[J]. 西北大学学报:自然科学版,2010,40(6):1017-1019.
[16] 黄载福,喻宗源,束家有. 饱和漆酚冠醚的研究进展[J]. 有机化学,1985,5(6):497-502.
[17] WANG C Z,HE Y F,ZHOU H,et al. Preparation and characterization of urushiol methylene acetal derivatives with various degrees of unsaturation in alkyl side chain[J]. International Journal of Polymer Science,2015,3:1-6.
[18] KIM D,JEON S L,SEO J. The preparation and characterization of urushiol powders (YPUOH) based on urushiol[J]. Progress in Organic Coatings,2013,76(10):1465-1470.
[19] EISOHLY M A,ADAWADKAR P D,BENIGNI D A,et al. Analogues of poison ivy urushiol. Synthesis and biological activity of disubstituted n-alkybenzenes[J]. Journal of Medicinal Chemistry,1986,29(5):606-611.
[20] 王冬晖,张萌,白卫斌,等. 具类辣素漆酚衍生物的制备及其抑菌性能[J]. 中国生漆,2015,34(3):47-51.
[21] ROBERTS D W,BENEZRA C. Quantitative structure-activity relationships for skin sensitization potential of urushiol analogues[J]. Contact Dermatitis,1993,29(2):78-83.
[22] JEFFERSON A,WANGCHAREONTRAKUL S. Long-chain phenols:Urushiol,laccol,thitsiol and phenylalkyl catechol compounds in burmese lac from melanorrhoea usitata[J]. Journal of Chromatography A,1986,367:145-154.
[23] 何源峰. 生漆漆酚的结构修饰及生物活性的研究[D]. 北京:中国林业科学研究院硕士学位论文,2013.
[24] HONG D H,HAN S B,LEE C W,et al. Cytotoxicity of urushiols isolated from sap of korean lacquer tree (Rhus vernicifera Stokes)[J]. Archives of Pharmacal Research,1999,22(6):638-641.
[25] LEE J C,KIM J,JANG Y S. Ethanol-eluted extract of Rhus verniciflua stokes inhibits cell growth and induces apoptosis in human lymphoma cells[J]. Journal of Biochemistry and Molecular Biology,2003,36(4):337-343.
[26] LUO L H,JIANG L P,GENG C Y,et al. Hydroquinone-induced genotoxicity and oxidative DNA damage in HepG2 cells[J]. Chemico-Biological Interactions,2008,173(1):1-8.
[27] KIM S,KIM D H,LEE S H,et al. Urushiol induces apoptosis via a p53-dependent pathway in human gastric cancer cells[J]. Journal of Cancer Prevention,2013,18(2):169-176.
[28] RYCKEWAERT L,SACCONNAY L,CARRUPT P A,et al. Non-specific SIRT inhibition as a mechanism for the cytotoxicity of ginkgolic acids and urushiols[J]. Toxicology Letters,2014,229(2):374-380.
[29] 杨梅,何江波,程永现,等. 3-[(Z)-十五碳-8-烯基]儿茶酚的全合成及其抗肿瘤血管生成活性研究[J]. 有机化学,2013,33(6):1319-1325.
[30] CHEN Y R,CHIOU R Y Y,LIN T Y,et al. Identification of an alkylhydroquinone from Rhus succedanea as an inhibitor of tyrosinase and melanogenesis[J]. Journal of Agricultural and Food Chemistry,2009,57(6):2200-2205.
[31] KIM J W,RYU K E,JANG H S,et al. Cytotoxic effect of urushiol-ethanol micro-particles on human cervical carcinoma cells[J]. Journal of Pharmaceutical Investigation,2004,34(1):23-27.
[32] CHOI J Y,PARK C S,CHOI J,et al. Cytotoxic effect of urushiol on human ovarian cancer cells[J]. Journal of Microbiology and Biotechnology,2001,11(3):399-405.
[33] KIM J Y,CHO J Y,MA Y K,et al. Nonallergenic urushiol derivatives inhibit the oxidation of unilamellar vesicles and of rat plasma induced by various radical generators[J]. Free Radical Biology and Medicine,2014,71:379-389.
[34] CHAKRABORTY A,FERK F,SIMIC T,et al. DNA-protective effects of sumach (Rhus coriaria L.),a common spice:Results of human and animal studies[J]. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis,2009,661(1):10-17.
[35] LEE J C,KIM J,LIM K T,et al. Ethanol eluted extract of Rhus verniciflua Stokes showed both antioxidant and cytotoxic effects on mouse thymocytes depending on the dose and time of the treatment[J]. BMB Reports,2001,34(3):250-258.
[36] HONG S H,SUK K T,CHOI S H,et al. Anti-oxidant and natural killer cell activity of Korean red ginseng (Panax ginseng) and urushiol (Rhus vernicifera Stokes) on non-alcoholic fatty liver disease of rat[J]. Food and Chemical Toxicology,2013,55:586-591.
[37] LIU C S,NAM T G,HAN M W,et al. Protective effect of detoxified Rhus verniciflua stokes on human keratinocytes and dermal fibroblasts against oxidative stress and identification of the bioactive phenolics[J]. Bioscience,Biotechnology,and Biochemistry,2013,77(8):1682-1688.
[38] JEONG S,KIM D,SEO J. Preparation and the antioxidant and antibacterial activities of urushiol powders (YPUOH)[J]. Progress in Organic Coatings,2014,77(5):981-987.
[39] SUK K T,KIM H S,KIM M Y,et al. In vitro antibacterial and morphological effects of the urushiol component of the sap of the Korean lacquer tree (Rhus vernicifera Stokes) on Helicobacter pylori[J]. Journal of Korean Medical Science,2010,25(3):399-404.
[40] SONG C H,CHUNG J B,JEONG B R,et al. Antifungal activity of crude extract compound from Rhus verniciflua against anthracnose fungi (Collectotrichum spp.) of red-pepper[J]. Korean Journal of Environmental Agriculture,2012,31(1):60-67.
[41] CHO J Y,PARK K Y,KIM S J,et al. Antimicrobial activity of the synthesized non-allergenic urushiol derivatives[J]. Bioscience,Biotechnology,and Biochemistry,2015,79(11):1915-1918.
[42] KADOKURA K,SURUGA K,TOMITA T,et al. Novel urushiols with human immunodeficiency virus type 1 reverse transcriptase inhibitory activity from the leaves of Rhus verniciflua[J]. Journal of Natural Medicines,2015,69(1):148-153.
[43] KIM M J,CHOI W C,BARSHINIKOV A M,et al. Inhibitory effects of the extract of Rhus verniciflua Stokes on the reverse transcriptase of AIDS[J]. Korean Journal of Medicinal Crop Science,2002,10(4):284-287.
[44] BANG C S,HONG S H,SUK K T,et al. Effects of Korean red ginseng (Panax ginseng),urushiol (Rhus vernicifera Stokes),and probiotics (Lactobacillus rhamnosus R0011 and lactobacillus acidophilus R0052) on the gut-liver axis of alcoholic liver disease[J]. Journal of Ginseng Research,2014,38(3):167-172. |