Synthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts
A group of homochiral imidazolium salts bearing hydrophobic camphor derived moiety and ester or amide functional group were synthesized and characterized. The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated...
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Veröffentlicht in: | Acta Facultatis Pharmaceuticae Universitatis Comenianae 2014-12, Vol.61 (2), p.42-48 |
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creator | Miklas, R Miklasova, N Bukovsky, M Devinsky, F |
description | A group of homochiral imidazolium salts bearing hydrophobic camphor derived moiety and ester or amide functional group were synthesized and characterized. The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated and compared to clinically used benzalkonium bromide (BAB) and carbethopendecinium bromide. The MIC values of amide derivatives 2a and 2b were slightly smaller than those for BAB, indicating their good activity. None of the prepared salts was more effective than carbethopendecinium bromide. The biocidal efficacy of amide derivatives was much higher compared to the ester analogues. |
doi_str_mv | 10.2478/afpuc-2014-0007 |
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The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated and compared to clinically used benzalkonium bromide (BAB) and carbethopendecinium bromide. The MIC values of amide derivatives 2a and 2b were slightly smaller than those for BAB, indicating their good activity. None of the prepared salts was more effective than carbethopendecinium bromide. The biocidal efficacy of amide derivatives was much higher compared to the ester analogues.</description><identifier>ISSN: 1338-6786</identifier><identifier>ISSN: 0301-2298</identifier><identifier>EISSN: 1338-6786</identifier><identifier>EISSN: 2453-6725</identifier><identifier>DOI: 10.2478/afpuc-2014-0007</identifier><language>eng</language><publisher>Bratislava: De Gruyter Open</publisher><subject>antimicrobial activity ; camphorsulfonic acid ; Chemical synthesis ; imidazolium salts ; Salt ; Sulfuric acid</subject><ispartof>Acta Facultatis Pharmaceuticae Universitatis Comenianae, 2014-12, Vol.61 (2), p.42-48</ispartof><rights>Copyright De Gruyter Open Sp. z o.o. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3112-1db06f7bf27c5f34706984be717469afac65eb58be6565fc8cc7ec5f7482f9493</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1698160426?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,21388,21389,27924,27925,33530,33744,43659,43805,64385,64389,72469</link.rule.ids></links><search><creatorcontrib>Miklas, R</creatorcontrib><creatorcontrib>Miklasova, N</creatorcontrib><creatorcontrib>Bukovsky, M</creatorcontrib><creatorcontrib>Devinsky, F</creatorcontrib><title>Synthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts</title><title>Acta Facultatis Pharmaceuticae Universitatis Comenianae</title><description>A group of homochiral imidazolium salts bearing hydrophobic camphor derived moiety and ester or amide functional group were synthesized and characterized. The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated and compared to clinically used benzalkonium bromide (BAB) and carbethopendecinium bromide. The MIC values of amide derivatives 2a and 2b were slightly smaller than those for BAB, indicating their good activity. None of the prepared salts was more effective than carbethopendecinium bromide. The biocidal efficacy of amide derivatives was much higher compared to the ester analogues.</description><subject>antimicrobial activity</subject><subject>camphorsulfonic acid</subject><subject>Chemical synthesis</subject><subject>imidazolium salts</subject><subject>Salt</subject><subject>Sulfuric acid</subject><issn>1338-6786</issn><issn>0301-2298</issn><issn>1338-6786</issn><issn>2453-6725</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkE1LxDAQhosoKLpnrwEvXuomaZqk4EUWv2DBgwreQppO3Ejb1KRV1l9v1vWwiIchc3jemcmTZacEX1Am5FzbYTI5xYTlGGOxlx2RopA5F5Lv7_SH2SzGt0RgTnnJ-FH28rjuxxVEF5Hum1Sj65wJvna6RUPwA4TRQUTeIqO7YeVDnFrre2eQNq5BDQT3AQ1KqUZ_-dZNHYq6HeNJdmB1G2H2-x5nzzfXT4u7fPlwe7-4WuamIITmpKkxt6K2VJjSFkxgXklWgyCC8UpbbXgJdSlr4CUvrZHGCEikYJLailXFcXa-nZuOfZ8gjqpz0UDb6h78FBWRVMiqEgwn9OwP-uan0KfrFElbCceM8kTNt1SyEGMAq4bgOh3WimC1ka1-ZKuNbLWRnRKX28Rn-jiEBl7DtE7Nzvj_k5xQRotvYneIBg</recordid><startdate>20141230</startdate><enddate>20141230</enddate><creator>Miklas, R</creator><creator>Miklasova, N</creator><creator>Bukovsky, M</creator><creator>Devinsky, F</creator><general>De Gruyter Open</general><general>De Gruyter Poland</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20141230</creationdate><title>Synthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts</title><author>Miklas, R ; Miklasova, N ; Bukovsky, M ; Devinsky, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3112-1db06f7bf27c5f34706984be717469afac65eb58be6565fc8cc7ec5f7482f9493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>antimicrobial activity</topic><topic>camphorsulfonic acid</topic><topic>Chemical synthesis</topic><topic>imidazolium salts</topic><topic>Salt</topic><topic>Sulfuric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miklas, R</creatorcontrib><creatorcontrib>Miklasova, N</creatorcontrib><creatorcontrib>Bukovsky, M</creatorcontrib><creatorcontrib>Devinsky, F</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>East Europe, Central Europe Database</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Acta Facultatis Pharmaceuticae Universitatis Comenianae</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miklas, R</au><au>Miklasova, N</au><au>Bukovsky, M</au><au>Devinsky, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts</atitle><jtitle>Acta Facultatis Pharmaceuticae Universitatis Comenianae</jtitle><date>2014-12-30</date><risdate>2014</risdate><volume>61</volume><issue>2</issue><spage>42</spage><epage>48</epage><pages>42-48</pages><issn>1338-6786</issn><issn>0301-2298</issn><eissn>1338-6786</eissn><eissn>2453-6725</eissn><abstract>A group of homochiral imidazolium salts bearing hydrophobic camphor derived moiety and ester or amide functional group were synthesized and characterized. The novel imidazolium bromides were tested as antimicrobial and antifungal agents and their minimal inhibitory concentration (MIC) was evaluated and compared to clinically used benzalkonium bromide (BAB) and carbethopendecinium bromide. The MIC values of amide derivatives 2a and 2b were slightly smaller than those for BAB, indicating their good activity. None of the prepared salts was more effective than carbethopendecinium bromide. The biocidal efficacy of amide derivatives was much higher compared to the ester analogues.</abstract><cop>Bratislava</cop><pub>De Gruyter Open</pub><doi>10.2478/afpuc-2014-0007</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antimicrobial activity camphorsulfonic acid Chemical synthesis imidazolium salts Salt Sulfuric acid |
title | Synthesis and antimicrobial properties of camphorsulfonic acid derived imidazolium salts |
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