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Journal of Biotechnology and Phytochemistry

Volume 1 Issue 3

Chemistry World 2017

Page 60

November 13-15, 2017 Athens, Greece

7

th

World Congress on

Chemistry

Cu(II) complexes of hydrazone Schiff base

ligands: synthesis, characterization, DNA and

topoisomerase i enzyme interactions

Ramazan Gup, Elif Eda Şengül

and

Cansu Gokce Topkaya

Mugla Sitki Kocman University, Turkey

Small inorganic complexes that can interact with DNA or

other biological molecules have tremendous conservation.

Because such compounds can pass the inhibitions that large

molecules cannot pass through to show desired activities. It is

a known phenomenon that transitionmetal complexes oxidize

or bind to DNA in the presence or absence of reductants.

Therefore, it is important to understand the structure activity

relationship especially in the antitumor action mechanism of

metal complexes that can bind to DNA under physiological

conditions and specifically cleave DNA. In particular, Cu(II)

complexes containing Schiff base are much more attractive

as they can enter into the bases of DNA. The interaction of

DNA with metal complexes is closely related to the design

of synthetic restorative enzymes and chemotherapeutic

drugs. Transitional metal complexes play a key role in the

formation of newly bound complexes in the DNA domain,

although structural flexibility and variable dimensionality are

taken into consideration. In recent years, the use of certain

chemotherapy drugs by interfering with topoisomerases in

cancer cells has focused on the enzyme topoisomerase I in the

development of anticancer drugs. In this study, new cationic

hydrazone Schiff bases and their coordination compounds

with Cu(II) have been synthesized and characterized. Firstly,

various p-substituted benzohydrazine derivatives were reacted

with cationic acetophenone derivatives, which were served

as a chelating bridge, in order to prepare hydrazone Schiff

base ligands. In the second step of this study, coordination

compounds of the synthesized ligands with biologically

important transition metal Cu(II) were isolated and

characterized. Then, inhibitory activities of topoisomerase

I enzyme and DNA binding and cleavage activities was

examined for the compounds. The effect of the factors such

as ligand and geometry tetrahedral square-planar, octahedral,

etc. on the activity where be defined. That the synthesis of

some Schiff base derivatives bearing functional groups such

as -OH and -NH

2

increasing the pharmacological activities

was discussed in this study. Consequently, novel and effective

agents interacting with DNA, showing topoisomerase

inhibitions activity have been revealed.

rgup@mu.edu.tr

J Biotech and Phyto 2017