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某些含双齿配体的过渡金属配合物的合成、光谱表征、DNA相互作用、抗癌及分子对接研究

Synthesis, spectral characterization, DNA interaction, anticancer and molecular docking studies on some transition metal complexes with bidentate ligand.

作者信息

Dhanaraj C Justin, Hassan Israr Ul, Johnson Jijo, Joseph J, Joseyphus R Selwin

机构信息

Department of Chemistry, University College of Engineering, Nagercoil (Anna University Constituent College), Nagercoil, 629004, Tamil Nadu, India.

Department of Research, College of Art and Applied Sciences, Dhofar University, P.O. Box 2509, PC 211 Salalah,Oman.

出版信息

J Photochem Photobiol B. 2016 Sep;162:115-124. doi: 10.1016/j.jphotobiol.2016.06.032. Epub 2016 Jun 21.

Abstract

The ligand, N(2),N(3)-bis(3-nitrophenyl)quinoxaline-2.3-diamine was prepared by the condensation of quinoxaline-2.3(1,4H)-dione with 3-nitroaniline. It was treated with Co(II), Ni(II), Cu(II) and Zn(II) acetates to form the metal complexes. These were characterized by elemental analysis, molar conductance, magnetic moment, UV-Vis., IR, (1)H NMR, ESR and mass spectral data. Octahedral geometry has been assigned to Co(II), Ni(II) and Zn(II) complexes, whereas Cu(II) complex has distorted octahedral geometry. From the powder XRD data, crystallite size and unit cell parameters were calculated. The surface morphology of the synthesized compounds were determined using SEM analysis. The antimicrobial activity of the compounds against some bacterial species viz. Escherichiacoli, Klebsiella pneumoniae, Pseudomonas aeuruginosa and Staphylococcus aureus; also the fungal species, Aspergillus niger, and Candida albicans were done by disc diffusion method. DNA binding, cleavage and super oxide anion scavenging activities were also evaluated. The DNA binding activity of the compounds were identified using electronic absorption titrations and DNA cleavage was determined using gel electrophoresis. The anticancer activities of the compounds against HeLa cell line were determined using MTT assay. The highly potent compound among the five against HeLa cell line is subjected to molecular docking study against human papilloma virus receptor molecule and ATP binding site of telomerase.

摘要

配体N(2),N(3)-双(3-硝基苯基)喹喔啉-2,3-二胺通过喹喔啉-2,3(1,4H)-二酮与3-硝基苯胺缩合制备而成。它与醋酸钴(II)、醋酸镍(II)、醋酸铜(II)和醋酸锌(II)反应形成金属配合物。通过元素分析、摩尔电导率、磁矩、紫外-可见光谱、红外光谱、(1)H核磁共振、电子自旋共振和质谱数据对这些配合物进行了表征。已确定钴(II)、镍(II)和锌(II)配合物为八面体几何构型,而铜(II)配合物具有扭曲的八面体几何构型。根据粉末X射线衍射数据计算了微晶尺寸和晶胞参数。使用扫描电子显微镜分析确定了合成化合物的表面形态。采用纸片扩散法测定了这些化合物对一些细菌物种,即大肠杆菌、肺炎克雷伯菌、铜绿假单胞菌和金黄色葡萄球菌的抗菌活性;还测定了对真菌物种黑曲霉和白色念珠菌的抗菌活性。还评估了DNA结合、切割和超氧阴离子清除活性。使用电子吸收滴定法鉴定了化合物的DNA结合活性,并使用凝胶电泳法测定了DNA切割活性。采用MTT法测定了这些化合物对HeLa细胞系的抗癌活性。对HeLa细胞系活性最强的五种化合物之一针对人乳头瘤病毒受体分子和端粒酶的ATP结合位点进行了分子对接研究。

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