Effects of polar substituents on the biological activity of thiosemicarbazone metal complexes

J Inorg Biochem. 2018 Feb:179:60-70. doi: 10.1016/j.jinorgbio.2017.11.009. Epub 2017 Nov 21.

Abstract

In this paper, citronellal, vanillin and pyridoxal thiosemicarbazones were modified with polar substituents, namely ethylmorpholine and glucose, to increase their polarity and compare the effects of these moieties on their biological activity. Altogether, nine ligands were synthesized and for each of them also their copper(II) and nickel(II) complexes were prepared and used for the biological tests. Eventually, assays on proliferation inhibition were conducted using leukemic cell line U937, already used as a model for previous citronellal thiosemicarbazone tests. Biological tests were also performed on solid tumor cell line HT29. From the first screenings, two of the metal complexes showed remarkable interesting properties, and, therefore, were also tested for histosensitivity.

Keywords: Anticancer; Copper(II); Histosensitivity; Metal complex; Nickel(II); Thiosemicarbazone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry
  • Coordination Complexes / pharmacology*
  • Copper / chemistry
  • Humans
  • Ligands
  • Molecular Structure
  • Nickel / chemistry
  • Thiosemicarbazones / chemical synthesis
  • Thiosemicarbazones / chemistry
  • Thiosemicarbazones / pharmacology*

Substances

  • Antineoplastic Agents
  • Coordination Complexes
  • Ligands
  • Thiosemicarbazones
  • Copper
  • Nickel