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全乙酰化表没食子儿茶素没食子酸酯的合成纯化及生物活性研究进展
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作者 刘苗苗 潘越 +2 位作者 范鑫 黄峻榕 曹云刚 《食品科学》 EI CAS CSCD 北大核心 2022年第19期330-337,共8页
表没食子儿茶素没食子酸酯(epigallocatechin-3-gallate,EGCG)是茶叶中重要的儿茶素成分,具有广泛的生物活性,但稳定性差、脂溶性差、生物利用度低,难以深度开发利用。乙酰化修饰是改善EGCG局限性的有效手段。全乙酰化表没食子儿茶素没... 表没食子儿茶素没食子酸酯(epigallocatechin-3-gallate,EGCG)是茶叶中重要的儿茶素成分,具有广泛的生物活性,但稳定性差、脂溶性差、生物利用度低,难以深度开发利用。乙酰化修饰是改善EGCG局限性的有效手段。全乙酰化表没食子儿茶素没食子酸酯(total acetylated epigallocatechin gallate,AcEGCG)是EGCG的全乙酰化修饰产物,其脂溶性和稳定性显著升高,生物利用度也更高,且其抗紫外线、细胞损伤修复以及抗癌等功能均优于EGCG,在食品、医药及化工领域应用前景广泛。本文综述了近期国内外关于AcEGCG的合成纯化方法、理化性质及相关生物活性研究进展,以期为后续AcEGCG的研究及开发利用提供参考。 展开更多
关键词 全乙酰化表没食子儿茶素没食子酸酯 合成纯化 理化性质 生物活性
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基质金属蛋白酶活性中心肽段的合成及纯化 被引量:1
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作者 高磊 李连之 李文智 《化学研究与应用》 CAS CSCD 北大核心 2009年第3期373-376,共4页
Matrix metalloproteinases(MMPs) are a large family of proteolytic enzymes which are involved in degradation of many different components of the extra cellular matrix.In this paper,the active center peptide domain of M... Matrix metalloproteinases(MMPs) are a large family of proteolytic enzymes which are involved in degradation of many different components of the extra cellular matrix.In this paper,the active center peptide domain of MMP-11 was synthesized by Fmoc-solid-phase synthesis method and purified by reversed-phase high performance liquid chromatography.The peptide was characterized by ESI-MS and 1H NMR. 展开更多
关键词 基质金属蛋白酶 活性中心 多肽 固相合成 纯化
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《药物合成设计与分离纯化技术》课程改革探索 被引量:5
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作者 崔成红 隋新安 《职业教育研究》 2013年第12期84-86,共3页
课程改革是提高教学质量的核心,也是教学改革的重点和难点。通过对《药物合成设计与分离纯化技术》课程在教学内容、教学方法、考核方式等方面进行改革,学生的学习兴趣和学习积极性得到了提高,课程改革取得了良好效果。
关键词 药物合成设计与分离纯化技术 课程改革 探索
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药物合成设计与分离纯化技术课程教学效能问卷调查 被引量:1
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作者 崔成红 隋新安 丛晓娟 《卫生职业教育》 2018年第3期112-114,共3页
目的比较强化训练法和任务卡片法与任务驱动法和讲授法产生的教学效能。方法期末就药物合成设计与分离纯化技术课程,对实验班和对照班学生进行问卷调查,比较两班对教学的评价。结果实验班学生对教学的评价显著高于对照班(P<0.05)。... 目的比较强化训练法和任务卡片法与任务驱动法和讲授法产生的教学效能。方法期末就药物合成设计与分离纯化技术课程,对实验班和对照班学生进行问卷调查,比较两班对教学的评价。结果实验班学生对教学的评价显著高于对照班(P<0.05)。结论实验班学生对所用教学方法产生的教学效能更加赞同。 展开更多
关键词 化学制药技术 教学效能 药物合成设计与分离纯化技术
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高职《药物合成设计与分离纯化技术》校本教材的结构设计
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作者 崔成红 隋新安 《广东化工》 CAS 2016年第22期196-197,203,共3页
山东药品食品职业学院的"药物合成设计与分离纯化技术"课程是一门职业特色课程。课程教师经过多年的教学改革与实践,编写完成了多元化的校本教材。文章介绍了主体教材的结构设计,教材内容任务化,便于实施理实一体化教学。
关键词 高职 药物合成设计与分离纯化技术 校本教材 结构设计
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高职“药物合成设计与分离纯化技术”课程校本教材开发的背景与思路
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作者 崔成红 隋新安 《青岛职业技术学院学报》 2016年第5期45-48,共4页
校本教材开发是高职教研教学中的重要工作。山东药品食品职业学院的"药物合成设计与分离纯化技术"课程是一门根据用人单位需求和高职学生特点设立的特色课程,当前缺乏内容匹配、易于教学的教材。为了更好地实现课程教学目标,... 校本教材开发是高职教研教学中的重要工作。山东药品食品职业学院的"药物合成设计与分离纯化技术"课程是一门根据用人单位需求和高职学生特点设立的特色课程,当前缺乏内容匹配、易于教学的教材。为了更好地实现课程教学目标,培养专业人才,有必要开发校本教材。根据专业人才培养方案修订课程标准、根据课程标准设计教材内容、基于工作过程系统化设计教材结构的教材开发思路,为教材开发工作奠定了基础。 展开更多
关键词 高职 药物合成设计与分离纯化技术 校本教材 课程标准 教材开发
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紫外可见光谱协助快速纯化卟啉及金属卟啉的光催化取代基效应 被引量:1
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作者 赵新筠 闫浩宇 +3 位作者 唐佳城 陈伟萍 李长学 VICTOR Borovkov 《中南民族大学学报(自然科学版)》 CAS 北大核心 2021年第1期1-8,共8页
以丙酸为溶剂,吡咯与4-取代苯甲醛反应合成5,10,15,20-四(4-取代苯基)卟啉.根据卟啉Soret带和Q带的特点,用紫外可见光谱协助监测柱层析中满足特征谱带的流出组份,快速分离纯化卟啉.以5,10,15,20-四(4-甲氧羰基苯基)卟啉为配体,与不同金... 以丙酸为溶剂,吡咯与4-取代苯甲醛反应合成5,10,15,20-四(4-取代苯基)卟啉.根据卟啉Soret带和Q带的特点,用紫外可见光谱协助监测柱层析中满足特征谱带的流出组份,快速分离纯化卟啉.以5,10,15,20-四(4-甲氧羰基苯基)卟啉为配体,与不同金属离子反应得到金属卟啉,对其进行可见光降解有机污染物罗丹明B的活性评价,优选出活性高的金属离子,发现锆离子参与的金属卟啉催化效果最优.以5,10,15,20-四(4-取代苯基)卟啉为配体(取代基为OH、OCH3、COOMe、COOH、Cl、Br、H),与锆离子配位形成金属卟啉.对其可见光光催化降解罗丹明B活性的来研究取代基效应.结果显示4-位为羧基和酯基的锆卟啉具有高的光催化活性.因此基于金属卟啉的催化剂可以通过调控金属离子的种类、价态和配位状态以及卟啉分子外围取代基提高光催化活性,用于有机污染物的有效去除. 展开更多
关键词 紫外可见光谱 卟啉合成和快速纯化 金属卟啉 取代基效应 光催化
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薏苡仁提取物对脂肪酸合成酶体外抑制作用的实验研究 被引量:4
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作者 高晶 于飞 曾勇 《中国药理通讯》 2007年第3期16-16,共1页
目的:研究薏苡仁提取物对动物脂肪酸合成酶(FAS)的体外抑制作用。方法:从鸭肝中分离纯化脂肪酸合成酶,将薏苡仁油与酶在25℃混合反应后,测定剩余活性,与空白进行比较来研究薏苡仁提取物对FAS的体外抑制作用。结果:在以薏苡仁提... 目的:研究薏苡仁提取物对动物脂肪酸合成酶(FAS)的体外抑制作用。方法:从鸭肝中分离纯化脂肪酸合成酶,将薏苡仁油与酶在25℃混合反应后,测定剩余活性,与空白进行比较来研究薏苡仁提取物对FAS的体外抑制作用。结果:在以薏苡仁提取物10μl/ml与酶反应2h后FAS的全反应、酮酰还原反应、烯酰还原反应及AcAeCoA还原反应酶活力分别剩余8.2%、21.6%、39.5%和8.9%,并且薏苡仁油对酶的抑制与剂量相关。结论:体外试验证明薏苡仁油对动物FAS具有体外抑制作用,对酮酰还原反应和AcAcCoA还原反应的抑制作用比烯酰还原反应强。研究为支持薏苡仁提取物抑制FAS作用的新靶点,揭示薏苡仁提取物应用于癌症治疗的理论依据。 展开更多
关键词 薏苡仁 纯化脂肪酸合成 鸭肝 体外抑制作用
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Three-dimensional Ordered Silica Colloidal Film Self-assembly Deposited on a VerticalSubstrate 被引量:2
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作者 刘丽霞 董鹏 +1 位作者 王晓冬 程丙英 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2003年第6期751-754,共4页
A method for preparation of particle crystal film constructed from monodisperse silica colloidal particles in diameter of about 300 nm is reported. The films were prepared from an ethanol suspension by vertical deposi... A method for preparation of particle crystal film constructed from monodisperse silica colloidal particles in diameter of about 300 nm is reported. The films were prepared from an ethanol suspension by vertical deposition that relies on capillary forces to assemble colloidal crystal particles on a vertical substrate. The 3D ordered films were characterized by transmission spectra and scanning electric microscope (SEM). The effect of evaporation temperature, particle concentration and sintered temperature on the quality of colloidal particle crystal film was investigated. 展开更多
关键词 colloidal Silica SELF-ASSEMBLE vertical deposition colloidal crystal
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Polysaccharides Purified from Wild Cordyceps Activate FGF2/FGFR1c Signaling 被引量:1
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作者 ZENG Yangyang HAN Zhangrun +2 位作者 YU Guangli HAO Jiejie ZHANG Lijuan 《Journal of Ocean University of China》 SCIE CAS 2015年第1期171-177,共7页
Land animals as well as all organisms in ocean synthesize sulfated polysaccharides. Fungi split from animals about 1.5 billion years ago. As fungi make the evolutionary journey from ocean to land, the biggest changes ... Land animals as well as all organisms in ocean synthesize sulfated polysaccharides. Fungi split from animals about 1.5 billion years ago. As fungi make the evolutionary journey from ocean to land, the biggest changes in their living environment may be a sharp decrease in salt concentration. It is established that sulfated polysaccharides interact with hundreds of signaling molecules and facilitate many signaling transduction pathways, including fibroblast growth factor (FGF) and FGF receptor signaling pathway. The disappearance of sulfated polysaccharides in fimgi and plants on land might indicate that polysaccharides without sulfation might be sufficient in facilitating protein ligand/receptor interactions in low salinity land. Recently, it was reported that plants on land start to synthesize sulfated polysaccharides in high salt environment, suggesting that fungi might be able to do the same when ex- posed in such environment. Interestingly, Cordyceps, a fungus habituating inside caterpillar body, is the most valued traditional Chi- nese Medicine. One of the important pharmaceutical active ingredients in Cordyceps is polysaccharides. Therefore, we hypothesize that the salty environment inside caterpillar body might allow the fungi to synthesize sulfated polysaccharides. To test the hypothesis, we isolated polysaccharides from both lava and sporophore of wild Cordyceps and also from Cordyceps militaris cultured without or with added salts. We then measured the polysaccharide activity using a FGF2/FGFRlc signaling-dependent BaF3 cell proliferation assay and found that polysaccharides isolated from wild Cordyceps activated FGF2/FGFR signaling, indicating that the polysaccha- rides synthesized by wild Cordyceps are indeed different from those by the cultured mycelium. 展开更多
关键词 POLYSACCHARIDE CORDYCEPS Cordyceps militaris FGF BaF3
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Human intestinal acyl-CoA synthetase 5 is sensitive to the inhibitor triacsin C 被引量:3
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作者 Elke Kaemmerer Anne Peuscher +4 位作者 Andrea Reinartz Christian Liedtke Ralf Weiskirchen Jürgen Kopitz Nikolaus Gassler 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第44期4883-4889,共7页
AIM:To investigate whether human acyl-CoA synthetase 5(ACSL5) is sensitive to the ACSL inhibitor triacsin C.METHODS:The ACSL isoforms ACSL1 and ACSL5 from rat as well as human ACSL5 were cloned and recombinantly expre... AIM:To investigate whether human acyl-CoA synthetase 5(ACSL5) is sensitive to the ACSL inhibitor triacsin C.METHODS:The ACSL isoforms ACSL1 and ACSL5 from rat as well as human ACSL5 were cloned and recombinantly expressed as 6xHis-tagged enzymes.Ni 2+-affinity purified recombinant enzymes were assayed at pH 7.5 or pH 9.5 in the presence or absence of triacsin C.In addition,ACSL5 transfected CaCo2 cells and intestinal human mucosa were monitored.ACSL5 expression in cellular systems was verified using Western blot and immunofluorescence.The ACSL assay mix included TrisHCl(pH 7.4),ATP,CoA,EDTA,DTT,MgCl 2,[9,103 H] palmitic acid,and triton X-100.The 200 μL reaction was initiated with the addition of solubilized,purified recombinant proteins or cellular lysates.Reactions were terminated after 10,30 or 60 min of incubation with Doles medium.RESULTS:Expression of soluble recombinant ACSL proteins was found after incubation with isopropyl betaD-1-thiogalactopyranoside and after ultracentrifugation these were further purified to near homogeneity with Ni 2+-affinity chromatography.Triacsin C selectively and strongly inhibited recombinant human ACSL5 protein at pH 7.5 and pH 9.5,as well as recombinant rat ACSL1(sensitive control),but not recombinant rat ACSL5(insensitive control).The IC50 for human ACSL5 was about 10 μmol/L.The inhibitory triacsin C effect was similar for different incubation times(10,30 and 60 min) and was not modified by the N-or C-terminal location of the 6xHis-tag.In order to evaluate ACSL5 sensitivity to triacsin C in a cellular environment,stable human ACSL5 CaCo2 transfectants and mechanically dissected normal human intestinal mucosa with high physiological expression of ACSL5 were analyzed.In both models,ACSL5 peak activity was found at pH 7.5 and pH 9.5,corresponding to the properties of recombinant human ACSL5 protein.In the presence of triacsin C(25 μmol/L),total ACSL activity was dramatically diminished in human ACSL5 transfectants as well as in ACSL5-rich human intestinal mucosa.CONCLUSION:The data strongly indicate that human ACSL5 is sensitive to triacsin C and does not compensate for other triacsin C-sensitive ACSL isoforms. 展开更多
关键词 Acyl-CoA synthetase 5 Fatty acid metabolism Mitochondria Triacsin C
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Synthesis and Re-refinement of Cu_3PSe_4
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作者 马宏伟 郭国聪 +4 位作者 周国伟 王明盛 林善伙 董振超 黄锦顺 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2002年第3期288-291,共4页
The title compound Cu3PSe4 was synthesized by the reaction of CuCl, P2Se5 and Se in a molar ratio of 1:1:1 at 500 C and structurally characterized by X-ray crystallography. The crystal belongs to orthorhombic, space g... The title compound Cu3PSe4 was synthesized by the reaction of CuCl, P2Se5 and Se in a molar ratio of 1:1:1 at 500 C and structurally characterized by X-ray crystallography. The crystal belongs to orthorhombic, space group Pmn21 with cell parameters: a = 7.685(2), b = 6.656(1), c = 6.377(1) , V = 326.2(1) 3, Z = 2, Dc = 5.472 g/cm3, Mr = 537.43, F(000) = 476, m = 32.12 mm-1, R = 0.0642, wR = 0.1481 and S = 1.037. The 3-D structure can be regarded as constructed from the alternately stacking of [Cu(2)Se4] tetrahedral layers and Cu(1)PSe tetrahedral layers along the b direction, in which the Cu(2)Se layer is comprised of corner-sharing [Cu(2)Se4] tetrahedra along the a and c directions, and the Cu(1)PSe layer is consisted of alternately corner-sharing [Cu(1)Se4] tetrahedra and [PSe4] tetrahedra along the a and c directions. 展开更多
关键词 solid state reaction normal tetrahedral structure metal chalcogenophosphide
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Structure Refinement of Samarium Tritellurides
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作者 池利生 邓水全 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1996年第4期267-269,共3页
The title compound was prepared from the corresponding elements(Sm, Te) using iodine as transport agent. The crystal structure was determined by the single crystal X-ray diffraction techniques with the crystal data as... The title compound was prepared from the corresponding elements(Sm, Te) using iodine as transport agent. The crystal structure was determined by the single crystal X-ray diffraction techniques with the crystal data as follows: SmTe3,M_r= 533. 15, orthorhombic. Cmcm, a=4. 323(2), b= 25. 613(3),c=4. 335(2) A,V=480. 0 A ̄3, Z=4, D_x=7. 38 g/cm ̄3, F(000) =872,μ= 300. 2 cm ̄(-1), R=0. 061,Rw.=0. 066 for 660 observed(I≥3σ(I)) unique reflections. The compound is isostructural with NdTe_3 ̄[1]. 展开更多
关键词 SYNTHESIS TELLURIDE crystal structure
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Synthesis and purification of long copper nanowires. Application to high performance flexible transparent electrodes with and without PEDOT:PSS 被引量:18
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作者 Celine Mayousse Caroline Celle Alexandre Carella Jean-Pierre Simonato 《Nano Research》 SCIE EI CAS CSCD 2014年第3期315-324,共10页
We demonstrate the hydrothermal synthesis of long copper nanowires based on a simple protocol. We show that the purification of the nanowires is very important and can be achieved easily by wet treatment with glacial ... We demonstrate the hydrothermal synthesis of long copper nanowires based on a simple protocol. We show that the purification of the nanowires is very important and can be achieved easily by wet treatment with glacial acetic acid. Fabrication of random networks of purified copper nanowires leads to flexible transparent electrodes with excellent optoelectronic performances (e.g., 55 Ω/sq. at 94% transparency). The process is carried out at room temperature and no post-treatment is necessary. Hybrid materials with the conductive polymer PEDOT:PSS show similar properties (e.g., 46 Ω/sq, at 93% transparency), with improved mechanical properties. Both electrodes were integrated in capacitive touch sensors. 展开更多
关键词 copper nanowires transparent electrodes PEDOT:PSS touch sensor metallic nanowires
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First way of enantioselective synthesis of moxifloxacin intermediate
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《Science China(Physics,Mechanics & Astronomy)》 SCIE EI CAS 2013年第3期307-311,共5页
A new method of enantioselective synthesis of (S,S)-2,8-diazobicyclo [4.3.0] nonane was found by using (R)-2-amino-2- phenyl-ethanol as chiral induction reagent. The entire synthetic process included 8 steps which... A new method of enantioselective synthesis of (S,S)-2,8-diazobicyclo [4.3.0] nonane was found by using (R)-2-amino-2- phenyl-ethanol as chiral induction reagent. The entire synthetic process included 8 steps which were easy to operate with high yield. The purification method was only simple recrystallization or even used directly in the next step without further purifica- tion. The total yield was 29%. 展开更多
关键词 enantioselective synthesis moxifloxacin intermediate (S S)-2 8-diazobicyclo [4.3.0] nonane
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