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Antibacterial Activity of Pipemidic Acid ions-MgFeAl Layered Double Hydroxide Hybrid Against E. coli and S. typhi 哌啶酸离子-镁铁层状双氢氧化物复合物对大肠杆菌和伤寒沙门氏菌的抑菌活性
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V60I2.74
Alejandra Santana-Cruz, J. Flores-Moreno, Roberto Guerra-González, M. Martínez-Ortiz
An anion exchange process was used to prepare pipemidic acid-MgFeAl composite from MgFeAl-Cl layered double hydroxide as inorganic matrix. The obtained hybrid material contains pipemidic acid anions as well as, in a less extent; carbonate and chloride species in its interlayer space. The antibacterial properties were evaluated against E. coli and S. typhi strains through dilution broth method. MgFeAl-Cl matrix resulted to be completely inactive against two bac-teria, while MgFeAl-PIP composite killed all colonies of E. coli after 90 min of exposure and showed a good activity to kill S. typhi bacteria at times as short as 120 min.
以MgFeAl-Cl层状双氢氧化物为无机基体,采用阴离子交换法制备了哌啶酸- mgfeal复合材料。所得到的杂化材料含有哌啶酸阴离子,以及在较小程度上;层间空间的碳酸盐和氯化物种类。采用稀释肉汤法测定其对大肠杆菌和伤寒沙门氏菌的抑菌性能。结果表明,MgFeAl-Cl基质对两种细菌完全无活性,而MgFeAl-PIP复合材料在暴露90分钟后杀死所有大肠杆菌菌落,并在短至120分钟的时间内显示出良好的杀灭伤寒沙门氏菌活性。
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引用次数: 2
A rapid, one-pot, multi-component Route to 4,4'-(arylmethylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ols) 快速、一锅、多组分合成4,4′-(芳基亚甲基)双(3-甲基-1-苯基- 1h -吡唑-5-醇)
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V59I1.6
A. Hassankhani
A new, efficient and environmentally benign protocol for the one-pot, multicomponent synthesis of 4,4’-arylmethylene-bis(3-methyl-1-phenyl-1H-pyr...
一种高效、环保的一锅多组分合成4,4′-芳基亚甲基-双(3-甲基-1-苯基- 1h -pyr的新工艺。
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引用次数: 8
Essential Metal-based drugs: Correlation between Redox Potential and Biological Activity of M2+ with a N2O2 Ligand 必需金属基药物:氧化还原电位与M2+与N2O2配体生物活性的相关性
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V61I2.258
Arturo Verduzco-Ramírez, Silvia Graciela Manzanilla-Dávila, María Eugenia Morales-Guillén, J. García-Ramos, Y. Toledaño-Magaña, Armando Marín-Becerra, M. Flores‐Álamo, L. Ortíz-Frade, Luis Fernando Olguín-Contreras, L. Ruiz-Azuara
One of the major public health problems worldwide is cancer followed by a significant number of deaths due to the resistance developed by bacteria or protozoan to the currently employed treatments. This generates an immediate need to develop drugs to treat these afflictions (illnesses, diseases). It has recently been identified that tumor cell, bacteria or protozoa are quite sensitive to oxidative stress induced by the same drugs. Due to this, it is important to develop new drugs to attend them, in this case, by using metals to increase the concentration of oxidative species. In the present work, the ligand 2,9-diformyl-4,7-diphenyl-1,10-phenanthroline and its corresponding coordination compounds with essential metals such as iron(II), cobalt(II), nickel(II), copper(II) and zinc(II) were synthesized. The electrochemical study shows that these compounds present three redox processes, all of them associated to the ligand. The compounds have shown inhibitory activity in vitro against human neuroblastoma CHP-212 cells, Escherichia coli and trophozoites of Entamoeba histolytica HM1:IMSS. It has been found that the inhibitory activity of the compounds studied is related to the first reduction process of the ligand. The correlation between the inhibitory activity and the red ox potential was linear. The inhibitory activity in CHP-212 increased with the increase of the compounds’ redox potential values, in contrast with the behavior observed in Escherichia coli , where the compounds with lowest redox potential values have had significantly higher inhibitory activity. Many of these coordination compounds have shown a higher inhibitory activity than those typically used in the treatment of cancer (cisplatin). The next step is to prove these compounds in vitro against healthy cells in order to verify its selectivity or cytotoxicity in these systems.
世界范围内的主要公共卫生问题之一是癌症,随后由于细菌或原生动物对目前采用的治疗方法产生耐药性而导致大量死亡。这就迫切需要开发药物来治疗这些痛苦(疾病、疾病)。近年来研究发现,肿瘤细胞、细菌或原生动物对同一种药物诱导的氧化应激均相当敏感。因此,开发新的药物来治疗它们是很重要的,在这种情况下,通过使用金属来增加氧化物种的浓度。本文合成了2,9-二甲酰-4,7-二苯基-1,10-菲罗啉配体及其与铁(II)、钴(II)、镍(II)、铜(II)、锌(II)等必需金属的配位化合物。电化学研究表明,这些化合物存在三个氧化还原过程,它们都与配体有关。这些化合物在体外对人神经母细胞瘤CHP-212细胞、大肠杆菌和溶组织内阿米巴滋养体HM1:IMSS具有抑制活性。研究发现,所研究化合物的抑制活性与配体的第一次还原过程有关。抑制活性与红牛电位呈线性相关。在CHP-212中的抑制活性随着化合物氧化还原电位值的增加而增加,而在大肠杆菌中观察到的行为则相反,氧化还原电位值最低的化合物具有明显更高的抑制活性。许多这些配位化合物已经显示出比那些通常用于治疗癌症(顺铂)更高的抑制活性。下一步是在体外对健康细胞证明这些化合物,以验证其在这些系统中的选择性或细胞毒性。
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引用次数: 5
Chromatin Bound PCNA is Complexed with Cell Cycle Protein Regulators as Determined by Chromatin Immunoprecipitation 染色质结合的PCNA与细胞周期蛋白调节因子络合,通过染色质免疫沉淀测定
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V56I1.268
N. Becerril, Miguel Ángel Martínez, E. García, Jorge Manuel Vázquez Ramos
Using the technique of Chromatin Immunoprecipitation, we have detected the formation of complexes between the homotrimer protein ring Proliferating Cell Nuclear Antigen, PCNA, and two fundamental regulators of the cell cycle, CdkA and Cyclin D4;2 along germination of maize seeds. This finding suggests the way PCNA participates in the control of the G1 phase, by allowing cyclin-kinase complexes to find and phosphorylate protein targets. Incidentally, PCNA may form a structure of a dimer of trimer when bound to the chromatin.
利用染色质免疫沉淀技术,我们在玉米种子萌发过程中检测到同源三聚体蛋白环增殖细胞核抗原(PCNA)与细胞周期的两个基本调控因子CdkA和Cyclin D4;2之间形成复合物。这一发现提示了PCNA参与G1期控制的方式,即允许细胞周期蛋白激酶复合物找到并磷酸化蛋白靶点。顺带一提,PCNA与染色质结合时可形成二聚体或三聚体的结构。
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引用次数: 2
Adsorption of chromium(VI) on radiation grafted N,N-dimethylaminoethylmethacrylate onto polypropylene, from aqueous solutions 辐射接枝聚丙烯上N,N-二甲氨基甲基丙烯酸乙酯对水溶液中铬的吸附研究
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V57I2.216
G. Burillo, J. Serrano-Gómez, J. Bonifacio-martinez
Polypropylene (PP) grafted with dimethylaminoethyl- methacrylate (DMAEMA), was prepared by irradiation with a 60 Co γ source. The obtained PP-g-DMAEMA was used to study the Cr(VI) ion adsorption as a function of contact time, initial pH, initial concen- tration of metal ion and temperature. Chromium adsorption data on PP-g-DMAEMA at various initial concentration fit well the Freundlich and Langmuir isotherms. The maximum adsorption capacity (amax) was found to be 0.3103 × 0 -4 mol g -1 . The thermodynamic parameters ΔH 0 , ΔG 0 and ΔS 0 were estimated showing the adsorption process to
用60 Co γ源辐照法制备了甲基丙烯酸二甲胺乙酯接枝聚丙烯(PP)。利用所制得的PP-g-DMAEMA研究了接触时间、初始pH、初始金属离子浓度和温度对Cr(VI)离子吸附的影响。PP-g-DMAEMA在不同初始浓度下对铬的吸附数据符合Freundlich和Langmuir等温线。最大吸附量(amax)为0.3103 × 0 -4 mol g -1。热力学参数ΔH 0, ΔG 0和ΔS 0表明吸附过程为
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引用次数: 9
Free radicals induced oxidative stress at a molecular level: the current status, challenges and perspectives of computational chemistry based protocols 自由基在分子水平上诱导氧化应激:基于计算化学方案的现状、挑战和前景
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V59I4.81
A. Galano
Oxidative stress is frequently caused by an excess of free radicals and has been associated with a wide variety of health disor-ders. Therefore, finding strategies for scavenging free radicals has be-come an active area of research. This review summarizes, from a physicochemical perspective, relevant strategies to fight oxidative stress via antioxidants, including prevention, deactivation of oxidants, and repair of damaged targets. Different reaction mechanisms in-volved in the chemical protection exerted by antioxidants are dis-cussed, as well as their relative importance depending on several aspects. Some of them are the polarity of the environment, the pH of aqueous phase, and the chemical nature of the reacting radicals. Data that can currently be obtained from computational, quantum, chemis-try, protocols are detailed and their reliability is analyzed. Viable crite-ria to identify optimal antioxidants using such protocols are provided. Current challenges and future directions in this area of research are discussed. A large set of antioxidants are compared and their trends in activity, based on kinetic data, is provided.
氧化应激通常是由自由基过量引起的,并且与多种健康疾病有关。因此,寻找清除自由基的策略已成为一个活跃的研究领域。本文从物理化学的角度综述了抗氧化剂对抗氧化应激的相关策略,包括抗氧化剂的预防、失活和受损靶点的修复。本文从几个方面讨论了抗氧化剂在化学保护中的不同反应机制,以及它们的相对重要性。其中一些是环境的极性,水相的pH值,以及反应自由基的化学性质。详细介绍了目前可以从计算、量子、化学、协议中获得的数据,并分析了它们的可靠性。提供了使用这种方案确定最佳抗氧化剂的可行标准。讨论了该领域研究的当前挑战和未来方向。对一大类抗氧化剂进行了比较,并根据动力学数据给出了它们的活性趋势。
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引用次数: 101
Microstructural evolution of rapid solidified Al-Ni alloys 快速凝固Al-Ni合金的组织演变
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V60I2.75
Manuel Alejandro Martínez-Villalobos, I. Figueroa, M. Suárez, G. Rodríguez, Omar Novelo Peralta, G. Reyes, Ismeli Alfonso López, Jorge Alejandro Verduzco Martínez, C. Trujillo
In this study, Al-Ni alloy ribbons in hypoeutectic, euctectic and hypereutectic compositions were obtained by melt spinning. The microstructural changes of the samples, from the as-cast to rapid solid-ification processes at different Cu wheel tangential velocities were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The rapid solidification caused morphological transformation of the Al-Al3Ni microstructure from acicular in the as-cast condition to globular in the melt spun ribbons and the growth of the metastable Al9Ni2 intermetallic compound, which acted as reinforcing particles. Due to the increment of the Ni content and the presence of these intermetallic compounds, with size of ~5nm, distributed in the aluminum matrix, the hardness of the alloys significantly increased from the hypoeutectic (90 VHN) to the hypereutectic (205VHN) composition.
本研究采用熔体纺丝法制备了亚共晶、共晶和过共晶成分的铝镍合金带。采用x射线衍射、扫描电镜和透射电镜对不同铜轮切向速度下试样从铸态到快速固相的组织变化进行了表征。快速凝固导致Al-Al3Ni组织由铸态的针状组织转变为熔体纺丝带中的球状组织,并生长出亚稳的Al9Ni2金属间化合物,起到增强颗粒的作用。由于Ni含量的增加和分布在铝基体中的~5nm大小的金属间化合物的存在,合金的硬度从亚共晶(90 VHN)显著提高到过共晶(205VHN)。
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引用次数: 5
Catalytic Properties of Pure and K+-Doped CuO/MgO System Towards 2-Propanol Conversion 纯CuO/MgO体系和掺杂K+体系对2-丙醇转化的催化性能
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V57I1.235
S. A. El-Molla, G. El-Shobaky, N. H. Amin, M. N. Hammed, S. Sultan
CuO/MgO system having different compositions was pre- pared by impregnation method followed by calcination at 400-900 °C. The effect of CuO content, calcination temperature and doping with small amounts of K + species (1-3 mol %) on physicochemical, surface and catalytic properties of the system were investigated using XRD, adsorption of N2 at -196 °C, and conversion of isopropyl alcohol at 150-400 °C using a flow technique. The results revealed that the solids having the formulae 0.2 and 0.3 CuO/MgO calcined at 400 °C con- sisted of nanosized MgO and CuO as major phases together with Cu2O as minor phase. The BET-surface areas of different adsorbents are decreased by increasing CuO content, calcination temperature and K + - doping. MgO-support material showed very small catalytic activity in 2-propanol conversion. The investigated system behaved as selective catalyst for dehydrogenation of 2-propanol with selectivity > 80%. The catalytic activity increased by increasing CuO content and decreased by increasing the calcination temperature within 400-900 °C. K + - dop-
采用浸渍法制备了不同组分的CuO/MgO体系,并在400 ~ 900℃下进行了煅烧。采用XRD、N2在-196℃的吸附、150 ~ 400℃的流动技术转化异丙醇,考察了CuO含量、煅烧温度和少量K + (1 ~ 3 mol %)掺杂对体系理化性能、表面性能和催化性能的影响。结果表明:在400℃煅烧条件下,由纳米MgO和CuO为主相,Cu2O为次相组成的CuO/MgO配方为0.2和0.3;不同吸附剂的bet -表面积随CuO含量、煅烧温度和K +掺杂的增加而减小。mgo载体材料对2-丙醇转化的催化活性很小。该体系作为2-丙醇脱氢的选择性催化剂,选择性> 80%。在400 ~ 900℃范围内,随着CuO含量的增加,催化活性提高,随着焙烧温度的升高,催化活性降低。K + - p-
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引用次数: 8
Zn(BH4)2/Ac2O/DOWEX(R)50WX4: A Novel System for Acylalation of Aldehydes Zn(BH4)2/Ac2O/DOWEX(R)50WX4:一种新型醛酰化体系
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V58I2.183
D. Setamdideh
La acilalacion de aldehidos estructuralmente diferentes ha sido realizada empleando Zn(BH4)2/Ac2O/DOWEX(R)50WX4 como un sistema novedoso, en 1-5 min a temperatura ambiente, con excelentes rendimientos de los productos (92-97%)
以Zn(BH4)2/Ac2O/DOWEX(R)50WX4为原料,在室温下1-5 min内进行了结构不同醛的酰化反应,收率为92-97%
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引用次数: 0
Secondary Metabolites from Asclepias otarioides 芦笋的次生代谢物
Pub Date : 2017-10-12 DOI: 10.29356/JMCS.V59I1.14
E. Maldonado, Sonia Amador, V. Juárez-Jaimes
Chemical study of the aerial parts of Asclepias otarioides led to the isolation of four pentacyclic triterpenes and one cardenolide glycoside. This is the first report on the occurrence of the triterpenes 1, 3, and 4 in the genus Asclepias
通过化学分析,分离出4个五环三萜和1个核桃苷。本文首次报道了三萜1、3、4在芦笋属植物中的存在
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引用次数: 3
期刊
Revista de la Sociedad Química de Mexico
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