...
首页> 外文期刊>RSC Advances >Synthesis of 1,3,5-trisubstituted pyrazoline derivatives and their applications
【24h】

Synthesis of 1,3,5-trisubstituted pyrazoline derivatives and their applications

机译:合成1,3,5-三取代的吡唑啉衍生物及其应用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A series of 1,3,5-trisubstituted pyrazolines based homoleptic Ru(III) complexes of type [Ru(L1-7)(3)]center dot(PF6)(3) (L1-7 = pyrazoline ligands) have been synthesized and characterized by elemental analysis, electronic spectroscopy, conductance measurements, thermogravimetric analysis (TGA), electron paramagnetic resonance (EPR), fourier transform infrared (FT-IR) spectroscopy and liquid chromatography mass spectroscopy (LC-MS). Octahedral geometry around ruthenium has been assigned in all complexes using EPR and electronic spectral analysis. All complexes have been investigated for their interaction with Herring Sperm (HS) DNA utilizing an absorption titration (K-b = 2.42-6.07 x 10(5) M-1) and viscosity measurement study. The studies suggest the classical intercalative mode of binding. The DNA-binding property of the Ru(III) complexes was also investigated theoretically using a molecular docking study and suggests an intercalation binding mode between the complex and nucleotide base pairs. A cleavage study on pUC19 DNA has been performed by agarose gel electrophoresis. The results indicated that the Ru(III) complexes can more effectively promote the cleavage of plasmid DNA. The free ligands and their complexes have been evaluated for cytotoxicity activity against S. pombe cells at a cellular level. A comparative study of cellular level cytotoxicity values of the all compounds indicates that the metal complexes show better activity against S. pombe cells compared to the pyrazoline ligands. The complexes have been screened for their in vitro antibacterial activity against two Gram(+ve) and three Gram(-ve) microorganisms. Ru(III) complexes are good in vitro cytotoxic agents and 50% lethal concentration (LC50) values are in range of 5.296-7.925 mu g mL(-1). All newly synthesized Ru(III) complexes have been also evaluated for their in vitro antimalarial activity against Plasmodium falciparum strain [inhibition concentration (IC50) = 0.54-0.92 mu g mL(-1)].
机译:已经合成了一系列基于1,3,5-三取代的[Ru(L1-7)(3)]中央点(PF6)(3)(3)(L1-7 =吡唑啉配体)的复合物并以元素分析,电子光谱,电导测量,热重分析(TGA),电子顺磁共振(EPR),傅里叶变换红外(FT-IR)光谱和液相色谱质谱(LC-MS)。使用EPR和电子光谱分析的所有复合物中,钌周围的八面体几何形状已经分配。已经研究了所有复合物,用于利用吸收滴定(K-B = 2.42-6.07×10(5)M-1)和粘度测量研究的鲱鱼精子(HS)DNA相互作用。研究表明了古典的结合模式。在理论上,使用分子对接研究理论上研究了Ru(III)复合物的DNA结合性,并表明复合物和核苷酸碱基对之间的插层结合模式。通过琼脂糖凝胶电泳进行了PUC19 DNA的切割研究。结果表明,Ru(III)复合物可以更有效地促进质粒DNA的切割。已经在细胞水平下评估了自由配体及其复合物针对S.Pombe细胞的细胞毒性活性。所有化合物的细胞水平细胞毒性值的对比研究表明,与吡唑啉配体相比,金属配合物对S.Pombe细胞进行了更好的活性。已经筛选复合物,其对两克(+ ve)和三克(-VE)微生物的体外抗菌活性。 Ru(iii)复合物在体外细胞毒性良好的良好体外毒剂,50%的致死浓度(LC50)值范围为5.296-7.925μg(-1)。还评估了所有新合成的Ru(III)复合物对疟原虫菌株的体外抗疟活动进行评估[抑制浓度(IC50)=0.54-0.92μg(-1)]。

著录项

  • 来源
    《RSC Advances》 |2015年第104期|共13页
  • 作者单位

    Sardar Patel Univ Dept Chem Anand Gujarat India;

    Sardar Patel Univ Dept Chem Anand Gujarat India;

    Sardar Patel Univ BR Doshi Sch Biasci Anand Gujarat India;

    Sardar Patel Univ BR Doshi Sch Biasci Anand Gujarat India;

    Sardar Patel Univ Dept Chem Anand Gujarat India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号