Heteroleptic Copper(I) Complexes of "scorpionate" Bis-pyrazolyl Carboxylate Ligand with Auxiliary Phosphine as Potential Anticancer Agents: An Insight into Cytotoxic Mode

  • Rais Ahmad Khan
  • , Mohammad Usman
  • , Rajakumar Dhivya
  • , Perumalsamy Balaji
  • , Ali Alsalme
  • , Hamad Allohedan
  • , Farukh Arjmand
  • , Khalid Alfarhan
  • , Mohammad Abdulkader Akbarsha
  • , Fabio Marchetti
  • , Claudio Pettinari
  • , Sartaj Tabassum*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

57 Scopus citations

Abstract

New copper(I) complexes [CuCl(PPh3)(L)] (1: L = LA = 4-carboxyphenyl)bis(3,5-dimethylpyrazolyl)methane; (2: L = LB = 3-carboxyphenyl)bis(3,5-dimethylpyrazolyl)methane) were prepared and characterised by elementaLAnalysis and various spectroscopic techniques such as FT-IR, NMR, UV-Vis, and ESI-MS. The molecular structures of complexes 1 and 2 were analyzed by theoretical B3LYP/DFT method. Furthermore, in vitro DNA binding studies were carried out to check the ability of complexes 1 and 2 to interact with native calf thymus DNA (CT-DNA) using absorption titration, fluorescence quenching and circular dichroism, which is indicative of more avid binding of the complex 1. Moreover, DNA mobility assay was also conducted to study the concentration-dependent cleavage pattern of pBR322 DNA by complex 1, and the role of ROS species to have a mechanistic insight on the cleavage pattern, which ascertained substantial roles by both hydrolytic and oxidative pathways. Additionally, we analyzed the potential of the interaction of complex 1 with DNA and enzyme (Topo I and II) with the aid of molecular modeling. Furthermore, cytotoxic activity of complex 1 was tested against HepG2 cancer cell lines. Thus, the potential of the complex 1 is promising though further in vivo investigations may be required before subjecting it to clinical trials.

Original languageEnglish
Article number45229
JournalScientific Reports
Volume7
DOIs
StatePublished - 24 Mar 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2017 The Author(s).

ASJC Scopus subject areas

  • General

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