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Novel 4-substituted phenyl-2,2'-bichalcophenes and aza-analogs as antibacterial agents: a structural activity relationship

Authors Hussin WA, Ismail MA, El-Sayed WM

Received 25 December 2012

Accepted for publication 6 February 2013

Published 22 March 2013 Volume 2013:7 Pages 185—193

DOI https://doi.org/10.2147/DDDT.S42073

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3


Warda A Hussin,1 Mohamed A Ismail,2,3 Wael M El-Sayed2,4

1
Al-Azhr University, Faculty of Science, Department of Botany and Microbiology, Cairo; 2King Faisal University, Faculty of Science, Departments of Biological Sciences and Chemistry, Al-Hufof, Ahsaa, KSA; 3Mansoura University, Faculty of Science, Department of Chemistry, Mansoura; 4University of Ain Shams, Faculty of Science, Department of Zoology, Abbassia, Cairo, Egypt

Abstract: Antibiotic resistance is a major health problem; therefore, new antibacterial agents will need to be continuously developed. A series of novel bichalcophenes has been tested and found to have antimicrobial activity against selected bacteria. Due to the promising antimicrobial effects of these 4-substituted phenyl bichalcophene derivatives, the study reported here was launched to examine the interaction between novel bichalcophenes and tetracycline. The minimum inhibitory concentration values for all bichalcophenes were between 8 and 64 µM. Many of the bichalcophenes had synergistic activity that increased the inhibitory effect of tetracycline against bacterial growth, as indicated by the fractional inhibitory concentration index. The post-antibiotic effects of the novel bichalcophenes were determined. Many bichalcophenes were able to elongate the period required for bacteria to recover and grow after a brief exposure to tetracycline. Escherichia coli did not develop resistance to many bichalcophenes over a period of 7 days. A structural activity relationship could be characterized, as monocationic derivatives were more active than the corresponding mononitriles. The presence of a pyridyl group and/or furan ring reduced the activity, while the presence of a phenyl or thiophene ring enhanced the antibacterial activity. Our results suggest that bichalcophenes could be useful to elevate the shelf life of many antibiotics.

Keywords: synergic interaction, fractional inhibitory concentration, post-antibiotic effect, resistant variants

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