Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/xmlui/handle/123456789/19155
Title: Synthesis, characterization, DNA binding and cytotoxicity of fluoro-dipyrrin based arene ruthenium(II) complexes
Authors: PAITANDI, RP
SINGH, RS
MUKHOPADHYAY, S
SHARMA, G
KOCH, B
VISHNOI, P
PANDEY, DS
Keywords: In-Vitro Dna
Anticancer Activity
Ir(Iii) Complexes
Aromatic-Hydrocarbons
Dna/Protein Binding
Spectral Properties
Molecular Docking
Protein-Binding
Metal-Complexes
Visible-Light
Issue Date: 2017
Publisher: ELSEVIER SCIENCE SA
Citation: INORGANICA CHIMICA ACTA,454,117-127
Abstract: Synthesis of four new arene ruthenium(II) complexes [(eta(6)-C10H14)RuCl(MFPdpm)] (1); [(eta(6)-C12H18)Ru-Cl (MFPdpm)] (2); [(eta(6)-C10H14)RuCl(PFPdpm)] (3) and [(eta(6)-C12H18)RuCl(PFPdpm)] (4) containing dipyrrin ligands 5-(4-fluoro)phenyldipyrromethene (MFPdpm) and 5-(penta-fluoro)phenyldipyrromethene (PFPdpm) have been described. The ligands and complexes have been thoroughly characterized by elemental analyses, spectroscopic studies (ESI-MS, IR, H-1, C-13 NMR, UV-Vis) and structure of the representative complex 4 determined by X-ray single crystal analyses. DNA binding activities of 1-4 have been investigated by UV-Vis and fluorescence spectroscopy and their binding through the minor groove of DNA has been established by molecular docking studies. The complexes 1-4 exhibit significant cytotoxicity toward human lung cancer cell line (A549). Cytotoxicity, morphological changes, and apoptosis studies have been evaluated through MIT assay, Hoechst 333421131 staining, and cell cycle analysis by fluorescence activated cell sorting (FACS). In vitro antitumor activity and cytotoxicity of the complexes lie in the order 4 > 3 > 2 > 1. (C) 2016 Elsevier B.V. All rights reserved.
URI: http://dx.doi.org/10.1016/j.ica.2016.03.003
http://localhost:8080/xmlui/handle/123456789/19155
ISSN: 0020-1693
1873-3255
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