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Submitted: 01 Jan 2020
Accepted: 25 Mar 2020
ePublished: 30 Mar 2020
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Avicenna J Clin Microbiol Infect. 2020;7(1): 15-21.
doi: 10.34172/ajcmi.2020.03
  Abstract View: 1162
  PDF Download: 699

Original Article

Synthesis and Antimicrobial Evaluation of the Potassium Salts of Benzhydrazine Dithiocarbamates

Hamid Beyzaei 1* ORCID logo, Sedigheh Esmaeilzadeh Bahabadi 2*, Shahla Najafi 2, Fahime Heidari Sadegh 2

1 Department of Chemistry, Faculty of Science, University of Zabol, Zabol, Iran.
2 Department of Biology, Faculty of Science, University of Zabol, Zabol, Iran.
*Corresponding Authors: Corresponding author: Hamid Beyzaei, Associate Professor, Department of Chemistry, Faculty of Science, University of Zabol, P.O. Box 538-98615, Zabol, Iran, Tel: +98 54 31232186, Fax: +98 54 31232180, E-mail: , Email: hbeyzaei@uoz.ac.ir; Corresponding author: Sedigheh Esmaeilzadeh Bahabadi, Associate Professor, Department of Biology, Faculty of Science, University of Zabol, P.O. Box 538-98615, Zabol, Iran, Tel: +98 54 31232187, Fax: +98 54 31232180, E-mail: , Email: esmaeilzadeh@uoz.ac.ir

Abstract

Background: New antimicrobial agents must be designed and synthesized for treating infectious diseases. In this study, antibacterial and antifungal activities of 6 potassium dithiocarbamates including three newly synthesized products were assessed on 10 bacterial and 3 fungal pathogens.

Methods: To this end, some benzhydrazine derivatives were reacted with carbon disulfide to afford dithiocarbamates, followed by applying diethyl ether and potassium hydroxide as solvent and base. Then, antimicrobial susceptibility tests were used to determine minimum inhibitory concentration, the minimum bactericidal concentration, and minimum fungicidal concentration values.

Results: The chemical structure of all synthesized dithiocarbamates were characterized with 1 H-, 13C-NMR (hydrogen-1 and 13-carbon nuclear magnetic resonance) and Fourier-transform infrared spectra. A variety of inhibitory effects was observed by the synthesized salts. Most synthetic dithiocarbamates affected bacterial strains and could efficiently block the proliferation of pathogenic fungi.

Conclusions: In general, prepared dithiocarbamates as potent chelating agents are able to interact with cell wall sulfur-containing compounds and the essential enzymes of microorganisms. In addition, the design of new hydrazine-based ligands and their corresponding complexes in future research can improve therapeutic properties. The evaluation of the cytotoxic effects of synthesized dithiocarbamates can also help their antimicrobial usages. Thus, these sulfur-rich and water-soluble salts are potential agents for combating plant pests.

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