Loading…

Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives

Derivatives of the thiazolidine-2,4-dione core represent a heterocyclic class with several correlated properties. In this context, the synthesis of structural analogues of these bioactive substances becomes attractive in the field of medicinal chemistry. These analogues act as antimicrobial agents a...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the Brazilian Chemical Society 2019, Vol.30 (1), p.164-172
Main Authors: de Paiva, Raíssa, da Silva, Jamerson, Moreira, Hudieyllen, Pinto, Osvaldo, Camargo, Lilian, Naves, Plínio, Camargo, Ademir, Ribeiro, Luciano, Ramos, Luciana
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3147-b28b937300778e12f09fa010868f2f7cad89a27edbd1fcf3ce89e34641dbe6193
cites
container_end_page 172
container_issue 1
container_start_page 164
container_title Journal of the Brazilian Chemical Society
container_volume 30
creator de Paiva, Raíssa
da Silva, Jamerson
Moreira, Hudieyllen
Pinto, Osvaldo
Camargo, Lilian
Naves, Plínio
Camargo, Ademir
Ribeiro, Luciano
Ramos, Luciana
description Derivatives of the thiazolidine-2,4-dione core represent a heterocyclic class with several correlated properties. In this context, the synthesis of structural analogues of these bioactive substances becomes attractive in the field of medicinal chemistry. These analogues act as antimicrobial agents against Gram-positives pathogens. The present work aimed to synthesize 10 different derivatives of 5-arylidene-thiazolidine-2,4-dione, employing urea as the catalyst in a solvent-free reaction medium, with yields that ranged from 45 to 99%. The compounds obtained were submitted to an antimicrobial assay against S. aureus ATCC 29213. Two compounds presented minimum inhibitory concentration of 62.5 and 32.5 µg mL-1 and minimum bactericidal concentration < 500 µg mL-1, demonstrating their antibacterial potential. Principal component analysis was carried out to discriminate the compounds in active and inactive classes. Four geometric and electronic molecular descriptors were required to completely discriminate the compounds. The selected descriptors can guide us in designing new 5-arylidene-thiazolidine-2,4-dione derivatives with enhanced activity.
doi_str_mv 10.21577/0103-5053.20180167
format article
fullrecord <record><control><sourceid>scielo_cross</sourceid><recordid>TN_cdi_scielo_journals_S0103_50532019000100164</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><scielo_id>S0103_50532019000100164</scielo_id><sourcerecordid>S0103_50532019000100164</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3147-b28b937300778e12f09fa010868f2f7cad89a27edbd1fcf3ce89e34641dbe6193</originalsourceid><addsrcrecordid>eNo9kMtqwzAQRUVpoenjC7rRB0SpHrYlL0P6hEChbtdClkdEwbGD5ARc-vFVmjabGe5w7wxzELpjdMZZLuU9ZVSQnOZixilTlBXyDE1SVSSTJT1Hk5PhEl3FuKaU57ngE_Rdjd2wgujjFM-7wW-8DX3tTYvndvB7P4zYdA2uhrCzwy4AOY3foTWD77u48lvcO1z1G8A5mYex9Q10QIaVN199Ej4JPs1Ik9yAHyD4fUruId6gC2faCLd__Rp9Pj1-LF7I8u35dTFfEitYJknNVV0KKSiVUgHjjpbOpIdUoRx30ppGlYZLaOqGOeuEBVWCyIqMNTUUrBTXaHbcG62Httfrfhe6dFBXByz6gCVhKylNMrHLUkAcAwlGjAGc3ga_MWHUjOpf4vqU1P_ExQ_wdXLq</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives</title><source>SciELO</source><creator>de Paiva, Raíssa ; da Silva, Jamerson ; Moreira, Hudieyllen ; Pinto, Osvaldo ; Camargo, Lilian ; Naves, Plínio ; Camargo, Ademir ; Ribeiro, Luciano ; Ramos, Luciana</creator><creatorcontrib>de Paiva, Raíssa ; da Silva, Jamerson ; Moreira, Hudieyllen ; Pinto, Osvaldo ; Camargo, Lilian ; Naves, Plínio ; Camargo, Ademir ; Ribeiro, Luciano ; Ramos, Luciana</creatorcontrib><description>Derivatives of the thiazolidine-2,4-dione core represent a heterocyclic class with several correlated properties. In this context, the synthesis of structural analogues of these bioactive substances becomes attractive in the field of medicinal chemistry. These analogues act as antimicrobial agents against Gram-positives pathogens. The present work aimed to synthesize 10 different derivatives of 5-arylidene-thiazolidine-2,4-dione, employing urea as the catalyst in a solvent-free reaction medium, with yields that ranged from 45 to 99%. The compounds obtained were submitted to an antimicrobial assay against S. aureus ATCC 29213. Two compounds presented minimum inhibitory concentration of 62.5 and 32.5 µg mL-1 and minimum bactericidal concentration &lt; 500 µg mL-1, demonstrating their antibacterial potential. Principal component analysis was carried out to discriminate the compounds in active and inactive classes. Four geometric and electronic molecular descriptors were required to completely discriminate the compounds. The selected descriptors can guide us in designing new 5-arylidene-thiazolidine-2,4-dione derivatives with enhanced activity.</description><identifier>ISSN: 0103-5053</identifier><identifier>ISSN: 1678-4790</identifier><identifier>EISSN: 1678-4790</identifier><identifier>DOI: 10.21577/0103-5053.20180167</identifier><language>eng</language><publisher>Sociedade Brasileira de Química</publisher><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><ispartof>Journal of the Brazilian Chemical Society, 2019, Vol.30 (1), p.164-172</ispartof><rights>This work is licensed under a Creative Commons Attribution 4.0 International License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3147-b28b937300778e12f09fa010868f2f7cad89a27edbd1fcf3ce89e34641dbe6193</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,4010,24131,27902,27903,27904</link.rule.ids></links><search><creatorcontrib>de Paiva, Raíssa</creatorcontrib><creatorcontrib>da Silva, Jamerson</creatorcontrib><creatorcontrib>Moreira, Hudieyllen</creatorcontrib><creatorcontrib>Pinto, Osvaldo</creatorcontrib><creatorcontrib>Camargo, Lilian</creatorcontrib><creatorcontrib>Naves, Plínio</creatorcontrib><creatorcontrib>Camargo, Ademir</creatorcontrib><creatorcontrib>Ribeiro, Luciano</creatorcontrib><creatorcontrib>Ramos, Luciana</creatorcontrib><title>Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives</title><title>Journal of the Brazilian Chemical Society</title><addtitle>J. Braz. Chem. Soc</addtitle><description>Derivatives of the thiazolidine-2,4-dione core represent a heterocyclic class with several correlated properties. In this context, the synthesis of structural analogues of these bioactive substances becomes attractive in the field of medicinal chemistry. These analogues act as antimicrobial agents against Gram-positives pathogens. The present work aimed to synthesize 10 different derivatives of 5-arylidene-thiazolidine-2,4-dione, employing urea as the catalyst in a solvent-free reaction medium, with yields that ranged from 45 to 99%. The compounds obtained were submitted to an antimicrobial assay against S. aureus ATCC 29213. Two compounds presented minimum inhibitory concentration of 62.5 and 32.5 µg mL-1 and minimum bactericidal concentration &lt; 500 µg mL-1, demonstrating their antibacterial potential. Principal component analysis was carried out to discriminate the compounds in active and inactive classes. Four geometric and electronic molecular descriptors were required to completely discriminate the compounds. The selected descriptors can guide us in designing new 5-arylidene-thiazolidine-2,4-dione derivatives with enhanced activity.</description><subject>CHEMISTRY, MULTIDISCIPLINARY</subject><issn>0103-5053</issn><issn>1678-4790</issn><issn>1678-4790</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNo9kMtqwzAQRUVpoenjC7rRB0SpHrYlL0P6hEChbtdClkdEwbGD5ARc-vFVmjabGe5w7wxzELpjdMZZLuU9ZVSQnOZixilTlBXyDE1SVSSTJT1Hk5PhEl3FuKaU57ngE_Rdjd2wgujjFM-7wW-8DX3tTYvndvB7P4zYdA2uhrCzwy4AOY3foTWD77u48lvcO1z1G8A5mYex9Q10QIaVN199Ej4JPs1Ik9yAHyD4fUruId6gC2faCLd__Rp9Pj1-LF7I8u35dTFfEitYJknNVV0KKSiVUgHjjpbOpIdUoRx30ppGlYZLaOqGOeuEBVWCyIqMNTUUrBTXaHbcG62Httfrfhe6dFBXByz6gCVhKylNMrHLUkAcAwlGjAGc3ga_MWHUjOpf4vqU1P_ExQ_wdXLq</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>de Paiva, Raíssa</creator><creator>da Silva, Jamerson</creator><creator>Moreira, Hudieyllen</creator><creator>Pinto, Osvaldo</creator><creator>Camargo, Lilian</creator><creator>Naves, Plínio</creator><creator>Camargo, Ademir</creator><creator>Ribeiro, Luciano</creator><creator>Ramos, Luciana</creator><general>Sociedade Brasileira de Química</general><scope>AAYXX</scope><scope>CITATION</scope><scope>GPN</scope></search><sort><creationdate>2019</creationdate><title>Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives</title><author>de Paiva, Raíssa ; da Silva, Jamerson ; Moreira, Hudieyllen ; Pinto, Osvaldo ; Camargo, Lilian ; Naves, Plínio ; Camargo, Ademir ; Ribeiro, Luciano ; Ramos, Luciana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3147-b28b937300778e12f09fa010868f2f7cad89a27edbd1fcf3ce89e34641dbe6193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>CHEMISTRY, MULTIDISCIPLINARY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Paiva, Raíssa</creatorcontrib><creatorcontrib>da Silva, Jamerson</creatorcontrib><creatorcontrib>Moreira, Hudieyllen</creatorcontrib><creatorcontrib>Pinto, Osvaldo</creatorcontrib><creatorcontrib>Camargo, Lilian</creatorcontrib><creatorcontrib>Naves, Plínio</creatorcontrib><creatorcontrib>Camargo, Ademir</creatorcontrib><creatorcontrib>Ribeiro, Luciano</creatorcontrib><creatorcontrib>Ramos, Luciana</creatorcontrib><collection>CrossRef</collection><collection>SciELO</collection><jtitle>Journal of the Brazilian Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Paiva, Raíssa</au><au>da Silva, Jamerson</au><au>Moreira, Hudieyllen</au><au>Pinto, Osvaldo</au><au>Camargo, Lilian</au><au>Naves, Plínio</au><au>Camargo, Ademir</au><au>Ribeiro, Luciano</au><au>Ramos, Luciana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives</atitle><jtitle>Journal of the Brazilian Chemical Society</jtitle><addtitle>J. Braz. Chem. Soc</addtitle><date>2019</date><risdate>2019</risdate><volume>30</volume><issue>1</issue><spage>164</spage><epage>172</epage><pages>164-172</pages><issn>0103-5053</issn><issn>1678-4790</issn><eissn>1678-4790</eissn><abstract>Derivatives of the thiazolidine-2,4-dione core represent a heterocyclic class with several correlated properties. In this context, the synthesis of structural analogues of these bioactive substances becomes attractive in the field of medicinal chemistry. These analogues act as antimicrobial agents against Gram-positives pathogens. The present work aimed to synthesize 10 different derivatives of 5-arylidene-thiazolidine-2,4-dione, employing urea as the catalyst in a solvent-free reaction medium, with yields that ranged from 45 to 99%. The compounds obtained were submitted to an antimicrobial assay against S. aureus ATCC 29213. Two compounds presented minimum inhibitory concentration of 62.5 and 32.5 µg mL-1 and minimum bactericidal concentration &lt; 500 µg mL-1, demonstrating their antibacterial potential. Principal component analysis was carried out to discriminate the compounds in active and inactive classes. Four geometric and electronic molecular descriptors were required to completely discriminate the compounds. The selected descriptors can guide us in designing new 5-arylidene-thiazolidine-2,4-dione derivatives with enhanced activity.</abstract><pub>Sociedade Brasileira de Química</pub><doi>10.21577/0103-5053.20180167</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0103-5053
ispartof Journal of the Brazilian Chemical Society, 2019, Vol.30 (1), p.164-172
issn 0103-5053
1678-4790
1678-4790
language eng
recordid cdi_scielo_journals_S0103_50532019000100164
source SciELO
subjects CHEMISTRY, MULTIDISCIPLINARY
title Synthesis, Antimicrobial Activity and Structure-Activity Relationship of Some 5-Arylidene-thiazolidine-2,4-dione Derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T14%3A08%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-scielo_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis,%20Antimicrobial%20Activity%20and%20Structure-Activity%20Relationship%20of%20Some%205-Arylidene-thiazolidine-2,4-dione%20Derivatives&rft.jtitle=Journal%20of%20the%20Brazilian%20Chemical%20Society&rft.au=de%20Paiva,%20Ra%C3%ADssa&rft.date=2019&rft.volume=30&rft.issue=1&rft.spage=164&rft.epage=172&rft.pages=164-172&rft.issn=0103-5053&rft.eissn=1678-4790&rft_id=info:doi/10.21577/0103-5053.20180167&rft_dat=%3Cscielo_cross%3ES0103_50532019000100164%3C/scielo_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3147-b28b937300778e12f09fa010868f2f7cad89a27edbd1fcf3ce89e34641dbe6193%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_scielo_id=S0103_50532019000100164&rfr_iscdi=true