Synthesis and characterization of heterobimetallic SnIV–CuII/ZnII complexes: DFT studies, cleavage potential and cytotoxic activity

  • Mohd Afzal
  • , Mohammad Usman
  • , Hamad A. Al-Lohedan
  • , Sartaj Tabassum*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Heterobimetallic complexes [Cu(L)Sn(CH3)2(H2O)(Cl)] (3) and [Zn(L)Sn(CH3)2(H2O)(Cl)] (4) have been synthesized from their monometallic analogs [Cu(L)(H2O)(Cl)] (1) and [Zn(L)(H2O)(Cl)] (2) of Schiff base ligand (L) which were characterized by various spectroscopic and analytical methods. DFT calculations were carried out to simulate the vibrational spectra to support the anticipated structures. The interaction studies of ligand (L) and complexes (1–4) with CT–DNA were performed by employing UV–vis, and fluorescence spectroscopic techniques which revealed that heterobimetallic complexes 3 and 4 showed higher affinity with DNA due to dual mode of action as compared to monometallic complexes 1 and 2. Further, validation of the interaction studies was accomplished by carrying out molecular docking studies with DNA. Gel assay displayed that both the complexes have ability to cleave DNA efficiently and are specific minor groove binders. CuII–SnIV complex 3 cleaved pBR322 DNA via oxidative mechanism, while ZnII–SnIV complex 4 followed hydrolytic cleavage pathway. In vitro cytotoxicity evaluation of complex 3 was tested on a different cancer cell lines showing promising antitumor activity. Communicated by Ramaswamy H. Sarma.

Original languageEnglish
Pages (from-to)1130-1142
Number of pages13
JournalJournal of Biomolecular Structure and Dynamics
Volume38
Issue number4
DOIs
StatePublished - 3 Mar 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.

Keywords

  • DFT
  • Heterobimetallic complexes
  • anticancer activity
  • in vitro DNA interaction studies
  • molecular docking

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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