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氨基酸侧链与氧化鸟嘌呤碱基对体系的氢键作用 被引量:1
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作者 韩冰玉 李月 刘翠 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2017年第6期1068-1075,共8页
应用量子化学方法,分别在气相和水溶液中对氨基酸侧链与氧化鸟嘌呤碱基对(8-oxo-G∶C)形成的三体复合物的氢键键能、几何结构、电荷分布及二阶稳定化能进行了研究.结果表明,水溶液的存在削弱了复合物中的氢键强度,电荷分布变化明显,水... 应用量子化学方法,分别在气相和水溶液中对氨基酸侧链与氧化鸟嘌呤碱基对(8-oxo-G∶C)形成的三体复合物的氢键键能、几何结构、电荷分布及二阶稳定化能进行了研究.结果表明,水溶液的存在削弱了复合物中的氢键强度,电荷分布变化明显,水溶液中形成氢键位点的电荷变化量约为气相中的10倍,而几何结构变化不明显、对于酶与DNA之间的相互作用的研究需在水溶液中进行.水溶液对带电三体复合物中8-oxo-G∶C与氨基酸侧链间的氢键有较大影响,键能平均减小了69.23 k J/mol,不带电复合物仅减小了3.60k J/mol.水溶液中三体复合物中8-oxo-G∶C间的氢键受侧链的影响不大,且与侧链带电与否无关,带电复合物和不带电复合物的氢键强度分别减小了24.57和30.05 k J/mol,且二阶稳定化能越大,其对应的氢键键长越短. 展开更多
关键词 氧化鸟嘌呤碱基 氨基酸侧链 氢键键能 自然键轨道理论 量子化学方法
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Fapy-G对碱基氢键复合物影响的理论研究 被引量:4
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作者 刘翠 张千慧 +2 位作者 宫利东 卢丽男 杨忠志 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2014年第12期2645-2653,共9页
应用量子化学方法对2,6-二氨基4-羟基-5.甲酰胺嘧啶(Fapy-G)与正常碱基作用形成的20种氧化碱基对的多种性质进行了理论分析,碱基G的c8位被氧化后N7和N9位分别增加一个H原子,使其由氢键受体变成氢键供体,N7,N9及06原子所带的电... 应用量子化学方法对2,6-二氨基4-羟基-5.甲酰胺嘧啶(Fapy-G)与正常碱基作用形成的20种氧化碱基对的多种性质进行了理论分析,碱基G的c8位被氧化后N7和N9位分别增加一个H原子,使其由氢键受体变成氢键供体,N7,N9及06原子所带的电荷变负,同时06作为氢键受体的能力增强.与碱基单体相比,碱基对中形成氢键的受体原子所带的电荷平均减小0.05e;供体H原子所带的电荷平均增大0.02e.Fapy—G分子中六元环上受体N原子参与形成氢键时,环的呼吸振动模式和N与对位C的振动模式的振动频率蓝移;与氢键相关的振动频率红移.所有氧化碱基对中,NH…N比NH…O氢键作用更强,且在NH…N氢键中,在六元环上的供体N原子形成的氢键比在氨基或开环上的供体N原子形成的氢键强.Fapy—G与碱基A作用结合能区域顺序为1〉2〉4〉3,与碱基T(R)作用区域顺序为3=4〉1〉2;水溶液使Fapy—G与碱基C作用的结合能减弱程度最大,结合能达到41.84—58.58kJ/mol,且使碱基对结合能力次序发生改变. 展开更多
关键词 量子化学方法 氧化碱基 氢键 电荷分布 结合能
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过渡金属配合物断裂双链DNA及其机理 被引量:4
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作者 刘长林 余四旺 +1 位作者 徐辉碧 周井炎 《无机化学学报》 SCIE CAS CSCD 北大核心 2000年第3期374-384,共11页
本文讨论了过渡金属配合物导致DNA双链断裂的各种攫氢反应及碱基氧化机理,对由水解过程促进DNA断裂的过渡金属配合物也作了介绍。
关键词 DNA 过渡金属配合物 攫氢 碱基氧化 水解
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Cr(VI)化合物引起DNA损伤的机制 被引量:2
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作者 王晓峰 徐立红 《环境与健康杂志》 CAS CSCD 北大核心 2006年第1期93-96,共4页
六价铬眼Cr(VI)演是一种公认的环境化学毒物,可导致多种类型的DNA损伤。但其本身并不能直接作用于DNA,它以氧阴离子形式通过非专一性的磷酸/硫酸阴离子通道透过细胞膜后经细胞内的还原剂还原形成一系列低价态铬,如五价铬眼Cr(V)演、四... 六价铬眼Cr(VI)演是一种公认的环境化学毒物,可导致多种类型的DNA损伤。但其本身并不能直接作用于DNA,它以氧阴离子形式通过非专一性的磷酸/硫酸阴离子通道透过细胞膜后经细胞内的还原剂还原形成一系列低价态铬,如五价铬眼Cr(V)演、四价铬眼Cr(IV)演和三价铬眼Cr(III)演。该文主要对Cr(VI)化合物进入体内后如何引起DNA损伤及DNA损伤类型作一概述。 展开更多
关键词 DNA损伤 自由基 碱基氧化
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Antoioxidant Activity of Carboxymethyl Chitosan with Different Substituted Degrees 被引量:15
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作者 姚倩 孙涛 +1 位作者 周冬香 毛芳 《Agricultural Science & Technology》 CAS 2008年第1期5-7,59,共4页
[Objective] In order to study the relations among different positions, degrees of substitution and antioxidant ability. [Method] N, O-carboxymethyl chitosan (NOA, NOB and NOC)with various degrees of substitution (D... [Objective] In order to study the relations among different positions, degrees of substitution and antioxidant ability. [Method] N, O-carboxymethyl chitosan (NOA, NOB and NOC)with various degrees of substitution (DS)were obtained by etherizing chito-oligosacchaside. Their structure and substituted degree were characterized and their antioxldant activity to·OH was evaluated. [ Result] The IC50 s of NOA ,NOB and NOC were 0.15 ,0. 29 ,0. 23 mg/ml while their DSs of -NH2 position(DSN) were 0.51,0.29 and 0.38 and DSo were 0. 74 ,0. 84 ,0. 97respectively.[ Conclusion] With the increase of DSN ,antioxidant activity of N,O-carboxymethyl chitosan oligosaccharide to·OH was up. 展开更多
关键词 Chitosan oligosaccharide Carboxymethyl chitosan oligosaccharide Degree of substitution Antioxidant activity
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Ethylbenzene to styrene over ZrO_2-based mixed metal oxide catalysts with CO_2 as soft oxidant 被引量:3
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作者 NanzheJiang Abhishek Burri Sang-Eon Park 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第1期3-15,共13页
ZrO2-based mixed metal oxide catalysts for the industrially important dehydrogenation process of ethylbenzene to styrene monomer have been explored by our group for the past 20 years.These efforts were subjected to th... ZrO2-based mixed metal oxide catalysts for the industrially important dehydrogenation process of ethylbenzene to styrene monomer have been explored by our group for the past 20 years.These efforts were subjected to the activation of CO2 over mixed metal oxide catalysts and resulted in several promising benefits to the dehydrogenation processes,such as stabilized conversion and selectivity,suppressed coke formation and commercially-acceptable longevity.In this review,we summarize the most recent developments on ZrO2-based mixed metal oxide catalysts,including the further optimization of sol-gel process in the synthesis of catalysts,rationalizing acid-base properties by doping,co-operative properties between redox and acid-base active sites and additional promoters towards the effective improvement of the longevity of catalysts. 展开更多
关键词 Oxidative dehydrogenation Carbon dioxide activation Zirconia-based mixed oxide Acid-base properties Redox properties
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Antioxidative activity of protein hydrolysates from anchovy
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作者 DING Li-jun LAI Xue-ling LIU Xiao-qing 《Journal of Chemistry and Chemical Engineering》 2008年第6期56-59,65,共5页
Alcalase hydrolyzed protein from Anchovy under controlled condition, and the hydrolysates were rich in active peptides. The peptide content was determined by TCA-biuret method, and amino acid was determined by Ninhydr... Alcalase hydrolyzed protein from Anchovy under controlled condition, and the hydrolysates were rich in active peptides. The peptide content was determined by TCA-biuret method, and amino acid was determined by Ninhydrin. The antioxidative activity of the hydrolysates was investigated by measuring the reducing ability, the inhibition of lipoxygenase activity, and antioxidative ability in linoleic acid oxidation system. The hydrolysates exhibited high antioxidative activity. In addition, the hydrolysates scavenged 58.38% on hydroxyl radical and 46.88% on superoxide radical. 展开更多
关键词 protein hydrolysatey PEPTIDES antioxidative activity free radicals ANCHOVY
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7,8-二氢-8-氧鸟嘌呤碱基对的量子化学研究 被引量:6
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作者 张千慧 王阳 +1 位作者 刘翠 杨忠志 《化学学报》 SCIE CAS CSCD 北大核心 2014年第8期956-962,共7页
遗传信息的完整性不断受氧化基因的威胁,7,8-二氢-8-氧鸟嘌呤(8-oxo-G)是氧化DNA损伤最常见的产物.氧化碱基会引起基因突变、癌变及衰老等.应用量子化学方法分析得出:鸟嘌呤(G)被氧化为8-oxo-G后,其电荷分布、氢键的供体和受体位点的数... 遗传信息的完整性不断受氧化基因的威胁,7,8-二氢-8-氧鸟嘌呤(8-oxo-G)是氧化DNA损伤最常见的产物.氧化碱基会引起基因突变、癌变及衰老等.应用量子化学方法分析得出:鸟嘌呤(G)被氧化为8-oxo-G后,其电荷分布、氢键的供体和受体位点的数目和位置随之改变,N7和O6原子所带的电荷变得更负,使得它们作为氢键供体的能力增强.从而G被误认为其他碱基,与正常碱基形成多种氢键复合物.可将8-oxo-G划分为3个作用位点与正常碱基相互作用.与正常的单体相比,碱基对中形成氢键的受体原子上所带电荷平均变负0.05e,占原电荷的8%;供体H原子所带电荷平均变正0.02e,占原电荷的4%.1位点与正常碱基作用形成的氢键复合物更稳定,2位点和3位点性质相似,水溶剂使碱基对的结合能力减弱,其中与C作用形成氢键复合物的结合能减弱程度最大,且使碱基对结合能力的次序改变.在8-oxo-G导致的GC→TA突变中,亲核反应位点从G所在链转到A(C)所在链,影响酶对碱基的识别,从而产生基因突变. 展开更多
关键词 从头算方法 氧化碱基 氢键 电荷分布 能量
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Efficient synthesis of thiohydantoin derivatives from amino acid esters and isothiocyanates in alkaline Al_2O_3
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作者 李刚 刘玉鹏 +3 位作者 雷蒙 王欣 程铁明 李润涛 《Journal of Chinese Pharmaceutical Sciences》 CAS 2012年第2期136-141,共6页
Various amino acid esters were reacted with different isothiocyanates in alkaline Al2O3 at room temperature for 1 h affording thiohydantoins in moderate to excellent yields.
关键词 THIOHYDANTOIN Amino acid ester ISOTHIOCYANATE Alkaline Al2O3 Synthesis
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Aluminum-based materials for advanced battery systems
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作者 Jiaqing Qiu Mingming Zhao +5 位作者 Qunxing Zhao Yuxia Xu Li Zhang Xin Lu Huaiguo Xue Huan Pang 《Science China Materials》 SCIE EI CSCD 2017年第7期577-607,共31页
There has been increasing interest in devel- oping micro/nanostructured aluminum-based materials for sustainable, dependable and high-efficiency electro- chemical energy storage. This review chiefly discusses the alum... There has been increasing interest in devel- oping micro/nanostructured aluminum-based materials for sustainable, dependable and high-efficiency electro- chemical energy storage. This review chiefly discusses the aluminum-based electrode materials mainly including A1203, AIF3, AIPO4, AI(OH)3, as well as the composites (carbons, silicons, metals and transition metal oxides) for lithium-ion batteries, the development of aluminum-ion batteries, and nickel-metal hydride alkaline secondary batteries, which summarizes the methodologies, related charge-storage mechanisms, the relationship between nanos- tructures and electrochemical properties found in recent years, latest research achievements and their potential ap- plications. In addition, we raise the relevant challenges in recently developed electrode materials and put forward new ideas for further development of micro/nanostructured aluminum-based materials in advanced battery systems. 展开更多
关键词 ALUMINUM BATTERY ELECTROCHEMICAL NANOMATERIAL
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