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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Main Authors: Surendra Babu Lagu, Rajendra Prasad Yejella, Richie R. Bhandare, Afzal B. Shaik
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/13/11/375
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spelling 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
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