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Synthesis and Spectral Characterization of Novel Spiroindan-1,3-Dione: A Diels Alder Adduct 新型螺藻丹-1,3-二酮:A Diels Alder加合物的合成与光谱表征
Pub Date : 2013-12-30 DOI: 10.1155/2013/415639
N. D. Zargar, K. Khan
DMSO/Ac2O reagent converts 1,3-indandione (1) to an unusual dimer 1H,1′H-2,2′-biindene-1,1′,3,3′(2H,2′H) tetrone and a dimeric condensation product along with an ylide (1a) at room temperature. This reagent also brings about oxidation of secondary alcohols to corresponding ketones, methyl thiomethylation, and N-hydroxymethylation in phthalimide and converts 4-hydroxycoumarins and dicoumarol to different oxidative and degradation products under varying conditions. However, when 1,3-indandione was refluxed with DMSO/Ac2O reagent at 150°C, it afforded a novel compound, 2-spiroindan 1,3-dione (2), a Diels Alder Adduct, analogous to (3) obtained upon treatment of 1,3-indandione with formaldehyde in presence of primary amines.
DMSO/Ac2O试剂在室温下将1,3-吲哚二酮(1)转化为不寻常的二聚体1H,1 ' h -2,2 ' -双茚二酮-1,1 ',3,3 ' (2H,2 ' h)四酮和二聚体与酰基化合物(1a)的缩合产物。该试剂还可使邻苯二胺中的仲醇氧化为相应的酮类、甲基硫甲基化和n -羟甲基化,并可在不同条件下将4-羟基香豆素和二oumarol转化为不同的氧化降解产物。然而,当1,3-茚二酮与DMSO/Ac2O试剂在150°C下回流时,它产生了一种新的化合物,2-旋螺酮1,3-二酮(2),一种Diels Alder加合物,类似于1,3-茚二酮在存在叔胺的情况下与甲醛处理后得到的(3)。
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引用次数: 0
Contribution of Ion-Exchange and Non-Ion-Exchange Reactions to Sorption of Ammonium Ions by Natural and Activated Aluminosilicate Sorbent 离子交换和非离子交换反应对天然和活化硅酸铝吸附剂吸附铵离子的贡献
Pub Date : 2013-12-25 DOI: 10.1155/2013/789410
L. I. Bel’chinskaya, L. Novikova, V. Khokhlov, Jen Ly Tkhi
The effect of acid and alkaline activation of complex natural aluminosilicate sorbent on its chemical composition, surface properties, and adsorption capacity towards ammonium ions was studied. An increase in specific surface area of the sorbent by 1.3 times after acid treatment and by 1.5 times after alkaline activation was shown. The change of ion-exchange complex of sorbent as a result of activation was observed. Sorption isotherms of ammonium ions on natural and activated samples were obtained and were satisfactorily described by the Langmuir equation. The evaluation and comparison of desorbed cations of alkali and alkaline earth metals were carried out. It was confirmed that ion-exchange processes primarily contributed to sorption of ammonium ions by natural and acid-activated silica-alumina, in contrast to alkali-activated one, for which absorption of nonexchangeable ammonium ions increased adsorption capacity of ammonium ions by 1.5 times.
研究了酸、碱活化对复合天然硅酸铝吸附剂的化学组成、表面性能和对铵离子吸附能力的影响。结果表明,酸活化后吸附剂的比表面积增加了1.3倍,碱活化后的比表面积增加了1.5倍。观察了吸附剂活化后离子交换络合物的变化。得到了铵离子在天然和活化样品上的吸附等温线,并用Langmuir方程对其进行了满意的描述。对碱金属和碱土金属的解吸阳离子进行了评价和比较。证实了离子交换过程对天然和酸活化的二氧化硅-氧化铝吸附铵离子的主要贡献,而碱活化的二氧化硅-氧化铝吸附非交换性铵离子的能力提高了1.5倍。
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引用次数: 23
Analgesic, Anti-Inflammatory, and Antiplatelet Profile of Hydrazones Containing Synthetic Molecules 含合成分子的腙类化合物的镇痛、抗炎和抗血小板谱
Pub Date : 2013-12-17 DOI: 10.1155/2013/247203
M. Asif, A. Husain
Hydrazones are present in many of the bioactive compounds with wide interest because of their diverse pharmacological applications. Hydrazones possess wide variety of biological activities such as anticonvulsant, antidepressant, analgesic, anti-inflammatory, antiplatelet, antimicrobial, anticancer, antihypertensive, anthelmintic, antidiabetic, antiparasitic, and other anticipated activities. This created an interest for researchers towards synthesized variety of hydrazone derivatives for different biological activities. Therefore many researchers have synthesized hydrazone derivatives as target structures for their biological activities. This is paper focuses on the analgesic, anti-inflammatory, and antiplatelet activities of hydrazones.
腙类化合物存在于许多生物活性化合物中,具有广泛的药理作用。腙类化合物具有广泛的生物活性,如抗惊厥、抗抑郁、镇痛、抗炎、抗血小板、抗菌、抗癌、降压、驱虫药、降糖、抗寄生虫等预期活性。这引起了研究人员对合成各种具有不同生物活性的腙衍生物的兴趣。因此,许多研究者合成了腙衍生物作为其生物活性的靶结构。本文主要研究腙类化合物的镇痛、抗炎和抗血小板活性。
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引用次数: 39
Green Extraction: Enhanced Extraction Yield of Asiatic Acid from Centella asiatica (L.) Nanopowders 绿色萃取:提高积雪草中积雪草酸的提取率摘要纳米
Pub Date : 2013-12-14 DOI: 10.1155/2013/460168
M. Z. Borhan, R. Ahmad, M. Rusop, S. Abdullah
Nanopowders of Centella asiatica (L.) were produced using planetary ball mill in order to investigate the differences of water extraction yield of asiatic acid as compared to micropowders of Centella asiatica. Effect of extraction time (20–60 min) on extraction yield of asiatic acid from Centella asiatica was examined. Results showed that water extraction of asiatic acid using Centella asiatica nanopowders exhibits was almost 50% higher extraction yield with 7.09 mg/g as compared to the micropowders of Centella asiatica. It was concluded that nanopowders contributed in enhancing water extraction yield of asiatic acid as compared to micropowders. Thereby utilizing nanopowders in water extraction could improve the extraction of asiatic acid via clean, eco-friendly, and less expensive process.
采用行星球磨机制备积雪草纳米粉末,研究积雪草微粉与积雪草微粉对积雪草酸水提率的差异。考察了提取时间(20 ~ 60 min)对积雪草中积雪草酸提取率的影响。结果表明,用积雪草纳米粉水提取积雪草酸,提取率为7.09 mg/g,比积雪草微粉水提取积雪草酸的提取率提高了近50%。实验结果表明,纳米粉末比微粉末更能提高亚细亚酸的水提率。因此,利用纳米粉末进行水萃取,可以通过清洁、环保和低成本的工艺提高亚细亚酸的提取效率。
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引用次数: 20
Development of Stability Indicating LC Method for the Estimation of Tolperisone in Bulk and Pharmaceutical Dosage Form 稳定性指示LC法测定原料药和制剂中托培里森酮的含量
Pub Date : 2013-12-10 DOI: 10.1155/2013/352984
U. Chhalotiya, K. Bhatt, D. Shah, S. Baldania, S. Patel
A rapid, specific, and sensitive reverse phase high performance liquid chromatographic method has been developed and validated for analysis of tolperisone in both bulk and pharmaceutical dosage form. The HPLC method was performed with a reversed phase C18 SunFire column (250 mm × 4.6 mm i.d., 5 mm particle size), detection at 261 nm and a mixture of methanol, water and pH 7.5 adjusted by use of 1% solution of triethylamine (60 : 40) as mobile phase. The flow rate was 1.0 mL min−1 and effluents were monitored at 261 nm. The retention time of tolperisone was 4.8 min. Tolperisone was subjected to acid and alkali hydrolysis, chemical oxidation, wet hydrolysis, dry heat degradation, and sunlight degradation. The degraded product peaks were well resolved from the pure drug peak with significant difference in their retention time values. Stressed samples were assayed using developed LC method. The proposed method was validated with respect to linearity, accuracy, precision, and robustness. The method was successfully applied to the estimation of tolperisone in tablet dosage forms.
建立了一种快速、特异、灵敏的反相高效液相色谱分析方法,并对其进行了验证。HPLC法采用反相C18 SunFire色谱柱(250 mm × 4.6 mm,粒径5 mm),在261 nm处检测,以1%三乙胺溶液(60:40)为流动相,调节甲醇、水和pH为7.5的混合物。流速为1.0 mL min - 1,在261 nm处监测流出物。托佩里松的保留时间为4.8 min。托佩里松经过酸碱水解、化学氧化、湿水解、干热降解和日光降解。降解产物峰与纯药峰分离较好,保留时间差异显著。采用开发的液相色谱法测定应力样品。该方法在线性度、准确度、精密度、鲁棒性等方面进行了验证。该方法成功地应用于片剂中托培里森酮的含量测定。
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引用次数: 2
Modification of Poly(ether ether ketone) Polymer for Fuel Cell Application 燃料电池用聚醚醚酮聚合物的改性研究
Pub Date : 2013-12-03 DOI: 10.1155/2013/386903
Devesh Shukla, Y. S. Negi, Vijai Kumar
Polyelectrolyte membrane (PEM) is an important part of PEM fuel cell. Nafion is a commercially known membrane which gives the satisfactory result in PEM fuel cell operating at low temperature. Present research paper includes functionalization of Poly(ether ether ketone) (PEEK) polymer with phosphonic acid group. The functionalization was done with the help of nickel-based catalyst. Further, the polymer was characterized by the FTIR, EDAX, DSC, TGA, and 1H NMR, and it was found that PEEK polymer was functionalized with phosphonic acid group with good thermal stability in comparison to virgin PEEK. Finally, the thin films of functionalized polymer were prepared by solution casting method, and proton conductivity of film samples was measured by impedance spectra whose value was found satisfactory with good thermal stability in comparison to commercially available Nafion membrane.
聚电解质膜(PEM)是PEM燃料电池的重要组成部分。Nafion是一种商业上已知的膜,在PEM燃料电池的低温运行中具有令人满意的效果。本文主要研究了磷酸基聚醚醚酮(PEEK)聚合物的功能化。在镍基催化剂的帮助下实现了功能化。通过FTIR、EDAX、DSC、TGA和1H NMR对聚合物进行表征,发现PEEK聚合物被磷酸基官能团所修饰,与未加工的PEEK相比具有良好的热稳定性。最后,采用溶液浇铸法制备了功能化聚合物薄膜,并通过阻抗谱测量了膜样品的质子电导率,与市售的Nafion膜相比,其值令人满意,具有良好的热稳定性。
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引用次数: 8
Naturally Occurring Xanthones: Chemistry and Biology 天然存在的山酮:化学和生物学
Pub Date : 2013-11-14 DOI: 10.1155/2013/621459
J. Negi, V. Bisht, P. Singh, M. Rawat, G. Joshi
Xanthones are one of the biggest classes of compounds in natural product chemistry. A number of xanthones have been isolated from natural sources of higher plants, fungi, ferns, and lichens. They have gradually risen to great importance because of their medicinal properties. This review focuses on the types, isolation, characterization, biological applications, and biosynthesis of naturally occurring xanthones isolated so far. Different physicochemical and instrumental methods such as liquid-solid and liquid-liquid extraction, TLC, flash chromatography, column chromatography, IR, 1H NMR and 13C NMR spectroscopy, GLC, HPLC, GC, and LCMS have been widely used for isolation and structural elucidation of xanthones. Hepatoprotective, anticarcinogenic, antileprosy, antimalarial, antioxidant, anticholinergic, mutagenicity, radioprotective, immunomodulatory, antibone resorption, antiparasitic, neuraminidase inhibitory, anticomplement, antibacterial, antifungal, algicidal, anti-HIV, cardioprotective, antitumoral, antidiabetes, antihyperlipidemic, antiatherogenic, anti-inflammatory, antiulcer, antidiabetic, hypolipidemic, analgesic, antiasthmatic, antihistaminic, antiamoebic, diuretic, antidiarrheal, larvicidal, and ovicidal activities have been reported for natural occurring xanthones. To a certain extent, this review provides necessary foundation for further research and development of new medicines.
山酮类化合物是天然产物化学中最大的一类化合物。从高等植物、真菌、蕨类植物和地衣等天然来源中已分离出许多山酮。由于它们的药用特性,它们逐渐变得非常重要。本文综述了迄今为止天然分离的山酮类化合物的类型、分离、表征、生物学应用和生物合成。液固萃取、液液萃取、薄层色谱、闪蒸色谱、柱层析、IR、1H NMR和13C NMR波谱、GLC、HPLC、GC、LCMS等不同的理化和仪器方法已广泛应用于山酮类化合物的分离和结构解析。保肝、抗癌、抗麻风病、抗疟、抗氧化、抗胆碱能、致突变性、辐射防护、免疫调节、抗骨吸收、抗寄生虫、神经氨酸酶抑制、抗补体、抗菌、抗真菌、杀藻、抗hiv、心脏保护、抗肿瘤、抗糖尿病、降血脂、抗动脉粥样硬化、抗炎、抗溃疡、降糖、降血脂、止痛、平喘、抗组胺、抗阿米巴、利尿剂、止泻剂、据报道,天然存在的山酮具有杀幼虫和杀卵活性。本综述在一定程度上为进一步研究和开发新药提供了必要的基础。
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引用次数: 149
Quantification of Benazepril Hydrochloride and Hydrochlorothiazide in Tablet Dosage Form by Simultaneous Equation Spectrophotometric Method 联立方程分光光度法定量测定片剂剂型中盐酸贝那普利和氢氯噻嗪的含量
Pub Date : 2013-09-16 DOI: 10.1155/2013/316137
Varsha Parmar, U. Chhalotiya, D. Shah, K. Bhatt, S. Baldania
Simple, accurate, precise, reproducible, requiring no prior separation, and economical procedures for simultaneous estimation of benazepril hydrochloride (BEN) and Hydrochlorothiazide (HCT) in tablet dosage form have been developed. Simultaneous equation method employs for estimation of both drugs in methanol at 240 nm and 270 nm as two analytical wavelengths. BEN and HCT at their respective (240 nm and 270 nm) show linearity in a concentration range of 2–12 μg/mL and 4–14 μg/mL. Recovery studies for BEN are 100.0–100.6% and 99.8–100.0% for HCT in the case of simultaneous equation method confirming the accuracy of the proposed method. The proposed method is recommended for routine analysis since it is rapid, simple, accurate and also sensitive and specific.
建立了一种简便、准确、精密度高、重复性好、无需预先分离、经济的同时测定片剂剂型盐酸苯那普利(BEN)和氢氯噻嗪(HCT)的方法。采用联立方程法在240 nm和270 nm两个分析波长处对两种药物在甲醇中的含量进行估计。BEN和HCT在各自波长(240 nm和270 nm)的浓度范围为2 ~ 12 μg/mL和4 ~ 14 μg/mL呈线性关系。联立方程法对BEN的回收率为100.0% ~ 100.6%,对HCT的回收率为99.8% ~ 100.0%,证实了所提方法的准确性。该方法具有快速、简便、准确、灵敏、特异等优点,可用于常规分析。
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引用次数: 2
Synthesis, Antimicrobial, and Anti-HIV1 Activity of Quinazoline-4(3H)-one Derivatives 喹唑啉-4(3H)- 1衍生物的合成、抗菌及抗hiv活性研究
Pub Date : 2013-09-12 DOI: 10.1155/2013/387191
K. Vijayakumar, A. J. Ahamed, G. Thiruneelakandan
The present investigation aims to synthesize 11 compounds of quinazoline-1 derivatives and to test their antimicrobial and anti-HIV1 activities. A quick-witted method was developed for the synthesis of novel substituted quinazolinone derivatives by summarizing diverse diamines with benzoxazine reactions, and it demonstrated the benefits of typical reactions, handy operation, and outstanding product yields. These compounds were confirmed by elemental analysis, I R, 1H NMR, 13C NMR, and mass spectra. Then antimicrobial and anti-HIV1 activities of the compounds were tested in-vitro. It was found that compounds 7–11 possessed a wide range of anti microbial and anti-HIV1 activity.
本研究旨在合成11个喹唑啉-1衍生物,并检测其抗菌和抗hiv活性。通过对不同二胺与苯并恶嗪反应的总结,建立了一种快速合成新型取代喹唑啉酮衍生物的方法,该方法反应典型,操作简便,产率高。这些化合物经元素分析、ir、1H NMR、13C NMR和质谱证实。体外检测化合物的抗菌和抗hiv活性。发现化合物7 ~ 11具有广泛的抗微生物和抗hiv活性。
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引用次数: 20
Study of Transport Properties of Tris (hydroxymethyl)aminomethane Hydrochloride in 20% (v/v) Acetone-Water System at 三(羟甲基)氨基甲烷盐酸盐在20% (v/v)丙酮-水体系中的输运性质研究
Pub Date : 2013-08-20 DOI: 10.1155/2013/820153
A. Dixit
Viscometric properties of Tris-(hydroxymethyl)amino methane hydrochloride are measured in 20% (v/v) acetone-water system 303.15°K. The related parameters are the experimental values of viscosity () allow to determine relative viscosity (), viscosity -coefficient of the Jones-Dole equation, free energies of activation of viscous flow and per mole solvent, and solute, respectively. The excess molar volume, excess viscosity, excess Gibb’s free energy, and interaction parameter of Grunberg and Nissan have also been calculated. These studies are of great help in characterizing the structure and properties of solutions. The addition of an organic solvent to water brings about a sharp change in the solvation of ions.
在20% (v/v)丙酮-水体系303.15°K中测定了Tris-(羟甲基)氨基甲烷盐酸盐的粘度。相关参数为粘度()的实验值,可分别确定相对粘度()、Jones-Dole方程的粘度系数、黏性流动激活自由能、每摩尔溶剂自由能和溶质自由能。计算了Grunberg和Nissan的超摩尔体积、超粘度、超吉布自由能和相互作用参数。这些研究对表征溶液的结构和性质有很大的帮助。在水中加入有机溶剂会使离子的溶剂化发生急剧变化。
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引用次数: 0
期刊
Journal of Chemical Technology & Biotechnology
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