Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives
Despite the availability of many drugs to treat infectious diseases, the problems like narrow antimicrobial spectrum, drug resistance, hypersensitivities and systemic toxicities are hampering their clinical utility. Based on the above facts, in the present study, we designed, synthesized and evaluat...
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doaj-1829afedaaf14f798a72406eaf3d10862020-11-25T04:09:00ZengMDPI AGPharmaceuticals1424-82472020-11-011337537510.3390/ph13110375Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone DerivativesSurendra Babu Lagu0Rajendra Prasad Yejella1Richie R. Bhandare2Afzal B. Shaik3Department of Pharmaceutical Sciences, Pharmaceutical Chemistry Division, A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam 530003, Andhra Pradesh, IndiaDepartment of Pharmaceutical Sciences, Pharmaceutical Chemistry Division, A.U. College of Pharmaceutical Sciences, Andhra University, Visakhapatnam 530003, Andhra Pradesh, IndiaDepartment of Pharmaceutical Sciences, College of Pharmacy & Health Sciences, Ajman University, Ajman P.O. Box 346, UAEDepartment of Pharmaceutical Chemistry, Vignan Pharmacy College, Vadlamudi 522213, Andhra Pradesh, IndiaDespite the availability of many drugs to treat infectious diseases, the problems like narrow antimicrobial spectrum, drug resistance, hypersensitivities and systemic toxicities are hampering their clinical utility. Based on the above facts, in the present study, we designed, synthesized and evaluated the antibacterial and antifungal activity of novel fluorinated compounds comprising of chalcones bearing trifluoromethyl (<b>A1</b>–<b>A10</b>) and trifluoromethoxy (<b>B1</b>–<b>B10</b>) substituents. The compounds were characterized by spectroscopic techniques and evaluated for their antimicrobial activity against four pathogenic Gram-positive (<i>Staphylococcus aureus</i> and <i>Bacillus subtilis</i>) and Gram-negative (<i>Escherichia coli</i> and <i>Bacillus subtilis</i>) bacterial and fungal (<i>Candida albicans</i> and <i>Aspergillus niger</i>) strains. In this study, the compounds with trifluoromethoxy group were more effective than those with trifluoromethyl group. Among the 20 fluorinated chalcones, compound <b>A3</b>/<b>B3</b> bearing an indole ring attached to the olefinic carbon have been proved to possess the most antimicrobial activity compared to the standard drugs without showing cytotoxicity on human normal liver cell line (L02). Further, the minimum inhibitory concentration (MIC) for <b>A3</b>/<b>B3</b> was determined by serial tube dilution method and showed potential activity. These results would provide promising access to future study about the development of novel agents against bacterial and fungal infections.https://www.mdpi.com/1424-8247/13/11/375fluorinated compoundschalconestrifluoromethyltrifluoromethoxyantibacterial activityantifungal activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Surendra Babu Lagu Rajendra Prasad Yejella Richie R. Bhandare Afzal B. Shaik |
spellingShingle |
Surendra Babu Lagu Rajendra Prasad Yejella Richie R. Bhandare Afzal B. Shaik Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives Pharmaceuticals fluorinated compounds chalcones trifluoromethyl trifluoromethoxy antibacterial activity antifungal activity |
author_facet |
Surendra Babu Lagu Rajendra Prasad Yejella Richie R. Bhandare Afzal B. Shaik |
author_sort |
Surendra Babu Lagu |
title |
Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives |
title_short |
Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives |
title_full |
Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives |
title_fullStr |
Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives |
title_full_unstemmed |
Design, Synthesis, and Antibacterial and Antifungal Activities of Novel Trifluoromethyl and Trifluoromethoxy Substituted Chalcone Derivatives |
title_sort |
design, synthesis, and antibacterial and antifungal activities of novel trifluoromethyl and trifluoromethoxy substituted chalcone derivatives |
publisher |
MDPI AG |
series |
Pharmaceuticals |
issn |
1424-8247 |
publishDate |
2020-11-01 |
description |
Despite the availability of many drugs to treat infectious diseases, the problems like narrow antimicrobial spectrum, drug resistance, hypersensitivities and systemic toxicities are hampering their clinical utility. Based on the above facts, in the present study, we designed, synthesized and evaluated the antibacterial and antifungal activity of novel fluorinated compounds comprising of chalcones bearing trifluoromethyl (<b>A1</b>–<b>A10</b>) and trifluoromethoxy (<b>B1</b>–<b>B10</b>) substituents. The compounds were characterized by spectroscopic techniques and evaluated for their antimicrobial activity against four pathogenic Gram-positive (<i>Staphylococcus aureus</i> and <i>Bacillus subtilis</i>) and Gram-negative (<i>Escherichia coli</i> and <i>Bacillus subtilis</i>) bacterial and fungal (<i>Candida albicans</i> and <i>Aspergillus niger</i>) strains. In this study, the compounds with trifluoromethoxy group were more effective than those with trifluoromethyl group. Among the 20 fluorinated chalcones, compound <b>A3</b>/<b>B3</b> bearing an indole ring attached to the olefinic carbon have been proved to possess the most antimicrobial activity compared to the standard drugs without showing cytotoxicity on human normal liver cell line (L02). Further, the minimum inhibitory concentration (MIC) for <b>A3</b>/<b>B3</b> was determined by serial tube dilution method and showed potential activity. These results would provide promising access to future study about the development of novel agents against bacterial and fungal infections. |
topic |
fluorinated compounds chalcones trifluoromethyl trifluoromethoxy antibacterial activity antifungal activity |
url |
https://www.mdpi.com/1424-8247/13/11/375 |
work_keys_str_mv |
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