abstract
Symmetric dinuclear chloro copper(II) complex [Cu(L)(Cl)(mu-Cl)](2) (1) and azo dinuclear azido copper(II) complex [Cu-2(L)(2)(N-3)(3)(mu(2)-N-3)](n) (2) [where L represents (5-methyl-pyrazol-1-ylmethyl)-napthalen-1-ylmethyl-amine] have been synthesized to examine the effect of napthyl group in the structure of pyrazole based dinuclear copper(II) complexes in DNA nuclease activity. The structure of 1 and 2 are characterized by X-ray crystallography, electrochemistry and various spectroscopic techniques. Coordinating ligand L is generated in situ from bis(3,5-dimethyl-pyrazol-1-ylmethyl)-napthalen-1-ylmethyl-amine (A) during complexation. Cytotoxic potential of free ligand (A), synthesized complexes 1, 2 and one cobalt(II) complex derived from ligand A, Co-II(A)Cl-2 (3) are analyzed using MTT cytotoxicity assay in U937 human monocytic cell line. Complexes 1 and 2 show very potent cytotoxicity (IC50 = 13-17 mu M); the best IC50 value is found for 1. LDH assay revealed that A and 3 has greater necrotic activity than the copper complexes. However, the results of DNA cleavage study clearly demonstrated that symmetric bridged dinuclear complexes with napthyl group lead to high level of nuclease activity 72-75% in the presence of glutathione. The bridged dinuclear copper(II) complexes undergo facile transformation to Cu(I) centre through inner sphere electron transfer mechanism (ISET) in presence of glutathione which facilitate the formation of free radicals/ions for DNA cleavage. Lacking of any reducible metal center in mononuclear cobalt(II) complex make it inactive towards free radicals generation in DNA cleavage activity.
keywords
CRYSTAL-STRUCTURE DETERMINATION; NITROGEN SINGLE BOND; STRAND SCISSION; RUTHENIUM COMPLEXES; ANTICANCER ACTIVITY; CU(II) COMPLEXES; CELL-DEATH; IN-VITRO; AGENTS; DERIVATIVES
subject category
Chemistry
authors
Jana, A; Brandao, P; Mondal, G; Bera, P; Santra, A; Jana, AD; Mokhamatam, RB; Manna, SK; Bhattacharyya, N; Bera, P
our authors
Paula Cristina Ferreira da Silva Brandão
Researcheracknowledgements
We are also thankful to Dr. Debabrata Maity, Department of Chemistry, Indian Institute of Technology, Bombay, India and Dr. Santanu Pattanayak of National Chemical Laboratory, Pune, India for EPR spectroscopy. Panskura Banamali College acknowledge the grant from DST, Govt. of India (No. SR-FIST-COLLEGE-295-dt18/11/2015).