SYNTHESIS, CHARACTERIZATION, COMPUTATIONAL STUDIES AND BIOLOGICAL ACTIVITY EVALUATION OF CU, FE, CO AND ZN COMPLEXES WITH 2-BUTANONE THIOSEMICARBAZONE AND 1,10-PHENANTHROLINE LIGANDS AS ANTICANCER AND ANTIBACTERIAL AGENTS

被引:18
作者
Khan, Tahmeena [1 ,2 ]
Azad, Iqbal [1 ]
Ahmad, Rumana [3 ]
Raza, Saman [2 ]
Dixit, Shalini [4 ]
Joshi, Seema [2 ]
Khan, Abdul Rahman [1 ]
机构
[1] Integral Univ, Dept Chem, POBas Ha,Kursi Rd, Lucknow 226026, UP, India
[2] Isabella Thoburn Coll, Dept Chem, 7 Faizabad Rd, Lucknow 226007, UP, India
[3] Era Univ, Eras Lucknow Med Coll & Hosp, Dept Biochem, Hardoi Rd, Lucknow 226003, UP, India
[4] CSIR Cent Inst Med & Aromat Plants, Dept Analyt Chem, PO CIMAP, Lucknow 226015, UP, India
来源
EXCLI JOURNAL | 2018年 / 17卷
关键词
Thiosemicarbazone; mixed; 1,10-phenanthroline; docking; bioactivity;
D O I
10.17179/excli2017-984
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mixed-ligand metal (II) (M=Cu, Fe, Co and Zn) complexes containing 2-butanone thiosemicarbazone and 1, 10-phenanthroline have been synthesized and characterized by melting point, FT-IR, H-1-NMR, UV-spectrophotometry and molar conductance measurements. All the complexes were soluble in DMSO and DMF. They were thermally stable with high melting points. The computational studies of the complexes were also performed to assess toxicity potential, bioactivity score prediction and drug likeliness assessment based on various drug filters. All the complexes showed no Veber's violations whereas only Cu complex showed one Lipinski's violation. Almost all synthesized compounds were predicted to have no toxic effects. Some of them showed positive bioactivity as enzyme inhibitors. Molecular docking of the complexes was also performed against ribonucleotide diphosphate reductase (RR) and topoisomerase II (Topo II) for minimum binding energy (kcal/mol) calculations. Cu complex was found to have minimum binding energy (-101.13 kcal/mol) released on interaction with Topo II showing a high affinity towards the enzyme, whereas Fe complex had the lowest binding energy (-99.8349 kcal/mol) when docked with RR. The results were compared with two standard drugs i.e. doxorubicin HCl and tetracycline. The ligand was tested for its potential anticancer activity against MDA-MB-231 cell line using MTT assay. Antibacterial activity of the complexes was tested against Staphylococcus aureus and Escherichia coli using the disc diffusion method. Cu (II) complex showed maximum activity against the MDA cells and also exhibited mild antibacterial activity against S. aureus.
引用
收藏
页码:331 / 348
页数:18
相关论文
共 16 条
[11]   Highly luminescent Cu(I)-phenanthroline complexes in rigid matrix and temperature dependence of the photophysical properties [J].
Felder, D ;
Nierengarten, JF ;
Barigelletti, F ;
Ventura, B ;
Armaroli, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (26) :6291-6299
[12]   A knowledge-based approach in designing combinatorial or medicinal chemistry libraries for drug discovery. 1. A qualitative and quantitative characterization of known drug databases [J].
Ghose, AK ;
Viswanadhan, VN ;
Wendoloski, JJ .
JOURNAL OF COMBINATORIAL CHEMISTRY, 1999, 1 (01) :55-68
[13]   ATOMIC PHYSICOCHEMICAL PARAMETERS FOR 3-DIMENSIONAL-STRUCTURE-DIRECTED QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS .2. MODELING DISPERSIVE AND HYDROPHOBIC INTERACTIONS [J].
GHOSE, AK ;
CRIPPEN, GM .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1987, 27 (01) :21-35
[14]  
Gupta R P, 1997, Pharm Acta Helv, V72, P43, DOI 10.1016/S0031-6865(96)00027-1
[15]   iGEMDOCK: a graphical environment of enhancing GEMDOCK using pharmacological interactions and post-screening analysis [J].
Hsu, Kai-Cheng ;
Chen, Yen-Fu ;
Lin, Shen-Rong ;
Yang, Jinn-Moon .
BMC BIOINFORMATICS, 2011, 12
[16]   Preparation and characterisation of new oxovanadium(IV) Schiff base complexes derived from amino acids and aromatic o-hydroxyaldehydes [J].
Pessoa, JC ;
Cavaco, I ;
Correia, I ;
Duarte, MT ;
Gillard, RD ;
Henriques, RT ;
Higes, FJ ;
Madeira, C ;
Tomaz, I .
INORGANICA CHIMICA ACTA, 1999, 293 (01) :1-11