This study describes
anticancer activity and DNA binding properties of partly (1) and fully (2a–g)
substituted spiro-cyclotriphosphazenes with a nitrogen-attached
4-hydroxyphenylethyl pendant arm. The reaction of
hexachlorocyclotriphosphazene, N3P3Cl6, with tyramine podand afforded
phosphazene (1). Heterocyclic amine substituted derivatives (2a–g) were
prepared by the replacement reactions of the Cl–atoms in 1 with pyrrolidine,
piperidine, morpholine, 1,4-dioxa-8-azaspiro[4,5]decane,
1-(2-aminoethyl)pyrrolidine, 1-(2-aminoethyl) piperidine, and
4-(2-aminoethyl)morpholine in dry THF, respectively. The DNA cleavage activity
of the compounds was studied on pBR322 DNA using gel electrophoresis
experiments. It was found that 2e and 2f had caused the highest level of damage
to DNA. The interactions of 1 and 2e with calf thymus DNA were also
investigated using absorption spectrometry. Computational studies were carried
out using DFT/B3LYP/6-31G method to know energies and the orientation of HOMO
and LUMO frontier orbitals of 1 and 2b. The obtained results revealed that
cyclotriphosphazene (1) interacted with DNA, further, this was also confirmed
by molecular docking evaluations. Molecular docking of 1 with the DNA gyrase
protein (PDB ID: 3U2D) exhibited the binding affinity with energy of −8.4
having an interaction with amino acids GLU-50 and ASN54. Cell death was
measured by using propidium iodide and Annexin V method on flow cytometry. Most
of cyclotriphosphazenes showed moderate cytotoxicity, while 2e and 2g had a
weak cytotoxicity on MDA-MB 231 human mammary cancer cell line.
This study was financially supported by The Scientific and
Technological Research Council of Turkey (Grant No. 113Z861).
Journal Section | Articles |
---|---|
Authors | |
Publication Date | February 16, 2017 |
Published in Issue | Year 2017 Volume: Volume 2 Issue: İssue 1 (1) - 2.İnternational Congress Of Forensic Toxicology |