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GC/MS同时检测人体尿液中可的宁和苯乙醇酸及苯乙醛酸的含量 被引量:9
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作者 吴鸳鸯 施卫星 陈枢青 《浙江大学学报(医学版)》 CAS CSCD 北大核心 2009年第3期229-234,共6页
目的:建立一种同时检测人尿样中可的宁(COT)、苯乙醛酸(PA)和苯乙醇酸(MA)含量的GC/MS分析方法。方法:采用GC/MS法,EI检测器,色谱柱为DB-5MS毛细管柱。进样前尿样先经过氯仿萃取,吹干后用MSTFA衍生化。结果:COT在0.0002-3.5μg... 目的:建立一种同时检测人尿样中可的宁(COT)、苯乙醛酸(PA)和苯乙醇酸(MA)含量的GC/MS分析方法。方法:采用GC/MS法,EI检测器,色谱柱为DB-5MS毛细管柱。进样前尿样先经过氯仿萃取,吹干后用MSTFA衍生化。结果:COT在0.0002-3.5μg.ml^-1呈线性关系,PA和MA在1.25-160μg.ml^-1呈线性关系,定量限分别为0.0002μg.ml^-1、1.25μg.ml^-1和1.25μg.ml^-1,回收率分别为89.53%-102.4%、84.88%-91.46%和83.46%-113.6%。结论:本实验室合并了尼古丁和苯乙烯这两种环境污染物的检测方法,而且定量下限与单个检测方法相当,可用于同时监控和测定尼古丁和苯乙烯对人体的危害。 展开更多
关键词 可替宁/尿 苯乙基醇/尿 苯乙烯/尿 醛类/尿 碎片质谱法/方法 色谱法 气相 环境污染物
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咖啡酸苯乙酯对实验性肝损伤大鼠的抗氧化作用 被引量:7
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作者 王秀芳 党双锁 +3 位作者 翟嵩 李亚萍 王文俊 赵丰 《临床肝胆病杂志》 CAS 2011年第8期856-859,864,共5页
目的探讨蜂胶提取物咖啡酸苯乙酯(CAPE)对四氯化碳(CCl4)等复合因素诱导的肝损伤大鼠的抗氧化作用。方法取95只健康雄性SD大鼠,随机分为9组。A:正常对照组;B:溶剂对照组,皮下注射橄榄油、腹腔注射10%乙醇,纯水灌胃;C:单纯模型组,腹腔注... 目的探讨蜂胶提取物咖啡酸苯乙酯(CAPE)对四氯化碳(CCl4)等复合因素诱导的肝损伤大鼠的抗氧化作用。方法取95只健康雄性SD大鼠,随机分为9组。A:正常对照组;B:溶剂对照组,皮下注射橄榄油、腹腔注射10%乙醇,纯水灌胃;C:单纯模型组,腹腔注射10%乙醇;D:维生素E组,10 mg/kg,腹腔注射,1次/d;E~I:CAPE(10%乙醇溶液)干预组:腹腔注射,3 mg/kg、6 mg/kg和12 mg/kg;灌胃,12 mg/kg和24 mg/kg,1次/d。C~I组均予以40%CCl4橄榄油溶液皮下注射、30%乙醇灌胃,高脂饲料作为单一饲料。同时每组给予对应药物处理10周。实验第10周处死大鼠。测定肝组织匀浆中氧化应激指标:丙二醛(MDA)、谷胱甘肽(GSH)水平以及过氧化氢酶(CAT)、超氧化物歧化酶(SOD)活力。肝组织标本行常规HE、Van Gieson染色。结果与单纯模型组的各项氧化应激指标相比较,腹腔注射CAPE 6、12 mg/kg两剂量组的肝组织中MDA含量明显降低、GSH水平升高、CAT和SOD活力增加(P<0.05)。腹腔注射CAPE 12 mg/kg组对肝脏氧化应激指标的改善程度比灌胃给药两个剂量组好(P<0.05)。腹腔注射CAPE 12 mg/kg组经HE和VG染色观察可见小部分区域肝细胞炎症坏死,少量纤维增生,较单纯模型组肝损伤程度轻。结论 CAPE可以抑制脂质过氧化,提高肝脏抗氧化能力。在本课题观察的剂量范围内,CAPE腹腔给药的抗氧化作用好于灌胃给药途径。 展开更多
关键词 肝疾病 咖啡酸类 苯乙基醇
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咖啡酸苯乙酯对糖尿病大鼠视网膜VEGF和ICAM-1表达的影响 被引量:4
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作者 袁鹏 臧婵媛 +1 位作者 周伟 刘学政 《天津医药》 CAS 北大核心 2011年第6期560-561,共2页
糖尿病视网膜病变(DR)是糖尿病最具破坏性的眼部并发症,DR可对视力造成不可挽回的影响,早期预防和治疗DR成为研究者关注的热点。咖啡酸苯乙酯(CAPE)是一种从蜂胶中分离出的酚类物质,具有抗炎、抗氧化应激和免疫调节作用,
关键词 糖尿病视网膜病变 苯乙基醇 咖啡酸类 血管内皮生长因子类 胞间黏附分子1 大鼠 Sprague—Dawley
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丙烯酸-2,4,6-三硝基苯乙酯的合成及热分解 被引量:2
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作者 刘强强 金波 +3 位作者 彭汝芳 舒远杰 楚士晋 董海山 《含能材料》 EI CAS CSCD 北大核心 2012年第5期579-582,共4页
以TNT、甲醛为原料,在弱碱性条件下反应合成得到2,4,6-三硝基苯乙醇(PicCH2CH2OH);PicCH2CH2OH在浓硫酸催化下和丙烯酸在甲苯中回流反应24h,合成得到丙烯酸-2,4,6-三硝基苯乙酯,产率为62%。采用紫外可见光谱(UV-Vis)、核磁共振氢谱(1HN... 以TNT、甲醛为原料,在弱碱性条件下反应合成得到2,4,6-三硝基苯乙醇(PicCH2CH2OH);PicCH2CH2OH在浓硫酸催化下和丙烯酸在甲苯中回流反应24h,合成得到丙烯酸-2,4,6-三硝基苯乙酯,产率为62%。采用紫外可见光谱(UV-Vis)、核磁共振氢谱(1HNMR)、红外光谱(FTIR)、质谱(MS)以及元素分析等对产物结构进行了表征。利用热重分析(TG)对产物热稳定性进行了研究,采用Kissinger方法和Ozawa方法计算其热分解活化能Ea分别为99.78,102.96kJ·mol-1。 展开更多
关键词 有机化学 2 4 6-三硝苯乙 丙烯酸-2 4 6-三硝苯乙 热稳定性 活化能
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Enantio-selective preparation of (S)-1-phenylethanol by a novel marine GDSL lipase MT6 with reverse stereo-selectivity 被引量:4
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作者 邓盾 张云 +1 位作者 孙爱君 胡云峰 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第11期1966-1974,共9页
We previously functionally characterized a novel marine microbial GDSL lipase MT6 and identified that the stereo-selectivity of MT6 was opposite to that of other common lipases in trans-esterification reactions.Herein... We previously functionally characterized a novel marine microbial GDSL lipase MT6 and identified that the stereo-selectivity of MT6 was opposite to that of other common lipases in trans-esterification reactions.Herein,we have investigated the use of MT6 in stereo-selective biocatalysis through direct hydrolysis reactions.Notably,the stereo-selectivity of MT6 was also demonstrated to be opposite to that of other common lipases in hydrolysis reactions.Parameters,including temperature,organic co-solvents,pH,ionic strength,catalyst loading,substrate concentration,and reaction time,affecting the enzymatic resolution of racemic 1-phenylethyl acetate were further investigated,with the e.e.of the final(S)-l-Phenylethanol product and the conversion being 97%and 28.5%,respectively,after process optimization.The lengths of side chains of 1-phenylethyl esters greatly affected the stereo-selectivity and conversion during kinetic resolutions.MT6 is a novel marine microbial GDSL lipase exhibiting opposite stereo-selectivities than other common lipases in both trans-esterification reactions and hydrolysis reactions. 展开更多
关键词 GDSLlipase BIOCATALYSIS Kinetic resolution Direct hydrolysis (S)-1-Phenylethanol Reverse stereo-selectivity
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Effect of 2-amino-2-[2-(4-octylphenyl) ethyl] propane- 1,3-diol hydrochloride (FTY 720) on immune liver injury in mice 被引量:5
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作者 Jing-HuaHe Hui-NaZhang Zhi-BinLin 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第4期573-576,共4页
AIM: To investigate the protective effect against two immune liver injury models in mice by 2-amino-2-[2-(4-octylphenyl) ethyl] propane-l,3-diol hydrochloride and its possible mechanisms in Con A-induced liver damage.... AIM: To investigate the protective effect against two immune liver injury models in mice by 2-amino-2-[2-(4-octylphenyl) ethyl] propane-l,3-diol hydrochloride and its possible mechanisms in Con A-induced liver damage. METHODS: Liver tissue or hepatocyte injury was monitored biochemically by measuring alanine aminotransferase (sALT) and aspartate aminotransferase (sAST) activity. Hematoxylin & eosin (HE) staining was used for histopathological examination. To evaluate the role of IFN-γ and IL-4 in the liver injury, serum levels of IFN-γ and IL-4 were determined using commercially available ELISA kit at 12 h after Con A challenge. We also determined FTY 720-induced spleen cell apoptosis by flow cytometry analysis or spleen cell proliferation test. RESULTS: Different doses of FTY 720 treatment dramatically reduced circulating markers of hepatocyte injury in two kinds of immunological liver injury models. FTY 720 dramatically reduced the elevated serum IFN-γ and IL-4 levels after Con A injection. Effect of spleen cell supernatants treated with Con A or FTY 720 on hepatocytes showed that ALT activities in cultured hepatocyte supernatants in Con A treatment group increased markedly and FTY 720 could reduce this elevated ALT activities in FTY 720 treatment group. FTY 720 dose-dependently increased the percentage of apoptotic cells in T cells and inhibited splenocyte proliferation induced by Con A. CONCLUSION: Pretreatment with FTY 720 was shown to produce protective effect on the immune liver injury in mice. The possible mechanism of FTY 720 on Con A-induced liver damage is that it could inhibit lymphocyte proliferation and induce lymphocyte apoptosis, resulting in the reduction of IL-4 or IFN-γ release, and subsequently protecting liver from being damaged by Con A. 展开更多
关键词 Immune liver injury FTY 720 Apoptosis Cell proliferation
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Asymmetric Bioreduction of 3,5-Bis(trifluoromethyl) Acetophenone to Its Corresponding Alcohol by Candida troplcalis 被引量:4
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作者 王普 苏会贞 +2 位作者 孙立明 何军邀 白亚萍 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2011年第6期1028-1032,共5页
(S)-3,5-bistrifluoromethylphenyl ethanol is a key chiral intermediate for the synthesis of NK-1 receptor antagonists. Enantioselective synthesis of (S)-3,5-bistrifluoromethylphenyl ethanol was successfully performed i... (S)-3,5-bistrifluoromethylphenyl ethanol is a key chiral intermediate for the synthesis of NK-1 receptor antagonists. Enantioselective synthesis of (S)-3,5-bistrifluoromethylphenyl ethanol was successfully performed in high enantiomeric excess (e.e.) through asymmetric reduction of 3,5-bis(trifluoromethyl) acetophenone catalyzed by Candida tropicalis 104 cells. The influence of some key reaction parameters such as substrate concentration, co-substrate and its concentration, biomass and reaction time was examined, respectively. The results showed that these factors obviously influence the yield, but the optical purity of the prepared product remains intact. The opti-mum conditions for the preparation of (S)-3,5-bistrifluoromethylphenyl ethanol were found to be as follows: sub-strate concentration 50 mmol?L?1; 50 g·L-1 of maltose as co-substrate; wet cell concentration 300 g·L-1; reaction for 30 h. Under above optimal conditions, the maximum yield for (S)-3,5-bistrifluoromethylphenyl ethanol reached 70.3% with 100% of product e.e. 展开更多
关键词 Candida tropicalis asymmetric reduction ENANTIOSELECTIVITY 3 5-bis(trifluoromethyl) acetophenone (S)-3 5-bistrifluoromethylphenyl ethanol
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Anti-inflammatory Activity and Antioxidant Potential of Aqueous Extracts from Stem Bark of Geoffroea decorticans
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作者 Maria Jofre Maria Fusco +5 位作者 Laura Favier Mauricio Teves Alejandra Rotelli Lilian Pelzer Claudia Ortega Diego Cifuente 《Journal of Pharmacy and Pharmacology》 2017年第10期703-707,共5页
In the present work we investigated, for the first time, the anti-inflammatory activity and the antioxidant properties of aqueous and ethanolic extracts, obtained from stem bark of Geoffroea decorticans (Gill. ex Hoo... In the present work we investigated, for the first time, the anti-inflammatory activity and the antioxidant properties of aqueous and ethanolic extracts, obtained from stem bark of Geoffroea decorticans (Gill. ex Hook. et Am.) Burk. (Fabaceae). G. decorticans, commonly known as "chafiar" or "chafiarcillo", is a traditional argentinean plant used as emollient, balsamic, antitussive, expectorant and anti-inflammatory. The stem bark was collected from San Francisco del Monte de Oro, San Luis, Argentina. Anti-inflammatory activity was evaluated by carrageenan-induced paw edema in rats. Antioxidant activity was tested using 1,1-Diphenyl-2-picrylhydrazyl radical-scavenging activity (DPPH), 2,2"-Azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) radical scavenging activity (ABTS) and ferric ion-reducing power (RP-Fe) assays. Aqueous extract 10% p/v showed anti-inflammatory activity (3h, 48% inhibition, 5h 37% inhibition and 7h 17% inhibition) and antioxidant activity (DPPH, ICs0 (mg/mL) = 0.098 =1: 0.032; ABTS, ICs0 (mg/mL) = 0.022 ~ 0.343, RP-Fe IC50 (mg/mL) = 1.124 ~ 0.146). In the other hand, the ethanolic extract 5% p/v, presented anti-inflammatory activity (3h, 34% inhibition, 5h 38% inhibition and 7h 35% inhibition) and antioxidant activity (DPPH, IC50 (mg/mL) = 0.133 q- 0.027; ABTS, IC50 (mg/mL) = 0.086 + 0.262, RP-Fe IC50 (mg/mL) = 7.089 ± 0.104). These results suggest that, also fruits, the aqueous and ethanolic extracts from the stem bark of G. decorticans present significant anti-inflammatory activity and antioxidant properties. 展开更多
关键词 Anti-inflammatory bioactivity antioxidant properties Geoffroea decorticans.
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Synthesis of biaryls using palladium nanoparticles immobilized on peptide nanofibers as catalyst and hydroxybenzotriazole as novel phenylating reagent
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作者 Arash Ghorbani-Choghamarani Zahra Taherinia 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2017年第3期469-474,共6页
Peptide nanofibers decorated with palladium nanoparticles catalyzed direct coupling of aryl halides with hydroxybenzotriazole to afford the corresponding biaryls in good to excellent yields.The coupling reactions proc... Peptide nanofibers decorated with palladium nanoparticles catalyzed direct coupling of aryl halides with hydroxybenzotriazole to afford the corresponding biaryls in good to excellent yields.The coupling reactions proceeded under simple,green,and mild conditions.The peptide nanofibers were used as recyclable supports in the coupling reactions.This approach is the first to use hydroxybenzotriazole as a phenylating agent. 展开更多
关键词 Peptide nanofiber Hydroxybenzotriazole BIARYL PEG Palladium
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SOLID PHASE SYNTHESIS OF ISOXAZOLINES
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作者 SUNWeimin LUOJuntao HUANG Wenqiang 《Chinese Journal of Reactive Polymers》 2002年第1期55-60,共6页
The solid-phase synthesis of isoxazolines on 2-polystyrylsulfonamidoethanol resin is reported. 2-Polystyrylsulfonamidoethanol resin 1 was reacted with acryloyl chloride to afford 2-polystyrylsulfonylamidoethyl acrylat... The solid-phase synthesis of isoxazolines on 2-polystyrylsulfonamidoethanol resin is reported. 2-Polystyrylsulfonamidoethanol resin 1 was reacted with acryloyl chloride to afford 2-polystyrylsulfonylamidoethyl acrylate resin 2, which was further reacted with brominated aldoximes by [3+2] cycloaddition to give isoxazoline resin 4. Resin 4 was treated with aqueous 6 mol/L HCl solution to obtain isoxazolines in good yield and purity. 展开更多
关键词 Solid phase synthesis 2-Polystyrylsulfonamidoethanol ISOXAZOLINE
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A Structure-properties Study of MDI-based Hydrophilic Polyether-polyester Polyurethane 被引量:1
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作者 权衡 顾振亚 吴穗生 《Journal of Donghua University(English Edition)》 EI CAS 2009年第4期408-412,共5页
A series of segmented polyether-polyester polyurethane with amorphous hydrophilic soft segment domains were prepared from 4,4'- diphenylmethane diisocyanate (MDI), polybutylene adipate (Glycol) 2000 (PBA2000), and... A series of segmented polyether-polyester polyurethane with amorphous hydrophilic soft segment domains were prepared from 4,4'- diphenylmethane diisocyanate (MDI), polybutylene adipate (Glycol) 2000 (PBA2000), and polyethylene glycol 1000 (PEG1000), with 1,4-butanediol (BDO) as the chain extender. Furthermore, several representative properties of the polyurethanes, such as moisture permeability, water resistance, hydrophilic property, and phase inversion temperature, were investigated. The studies show that the structure and concentration of soft segment have a remarkable effect on the main application properties of polyurethane. On the contrary, the functional properties of the polyurethane are almost not affected by its hard segment. 展开更多
关键词 hydrophilic polyurethane POLYETHER polyester structure property
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Synthesis and Crystal Structure of Carvedilol
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作者 CHEN Wei-Min XU Ji-Hong ( Institute of Pharmaceutical Sciences, the First Military Medical University,Guangzhou, 5l05l5) +3 位作者 ZENG Long-Mei ( Department of Chemistry, Zhongshan University ,Guangzhou 51O275) YU Kai-Bei ( Chengdu Institue of Analysis 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1998年第5期325-328,共4页
The crystal structure of the title compound carvedilol, C24H25N2O4(Mr= 406. 47), has determined by single-crystal X-ray diffraction. The crystal is mono-clinic with space group P21/c, a=9. 094(l), b= l2. 754(1), c= 18... The crystal structure of the title compound carvedilol, C24H25N2O4(Mr= 406. 47), has determined by single-crystal X-ray diffraction. The crystal is mono-clinic with space group P21/c, a=9. 094(l), b= l2. 754(1), c= 18. 330(2) A, β=97. 36(1 )°, V= 2l08. 5(4) A 3, Z= 4, D.= l. 280 g/cm3, F(000) = 864, μ=O. O88mm-1 and final R= O. O368, wR(F2) = 0.0787 for reflections (I>2σ(I) ). X-ray anal-ysis reveals that the crystal is composed of a pair of enantiomer, and there are hydrogenbonds O(3) -H(3O) -N(l ) between the two enantimers. There are two planes in themolecule. 展开更多
关键词 CARVEDILOL SYNTHESIS crystal structure
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Thermal and photoinduced valence tautomerism of a chain compound
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作者 CHEN LiQin WEI RongJia +2 位作者 TAO Jun HUANG RongBin ZHENG LanSun 《Science China Chemistry》 SCIE EI CAS 2012年第6期1037-1041,共5页
Herein reported is an example of one-dimensional coordination polymer [Co11(3,5-DBsq)2(dpg)]·(3,5-H2DBcat)2 (1) (3,5-DBsq = 3,5-di-tert-butylsemiquinonate, 3,5-H2DBcat = 3,5-di-tert-butyl-benzene-1,2-diol, dpg = ... Herein reported is an example of one-dimensional coordination polymer [Co11(3,5-DBsq)2(dpg)]·(3,5-H2DBcat)2 (1) (3,5-DBsq = 3,5-di-tert-butylsemiquinonate, 3,5-H2DBcat = 3,5-di-tert-butyl-benzene-1,2-diol, dpg = meso-alpha,beta-di(4-pyridyl)glycol) capable of undergoing thermal and photoinduced valence tautomeric transitions. 展开更多
关键词 valence tautomerism coordination polymer cobalt(II) photo excitation
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