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Towards smart biocide-free anti-biofilm strategies: Click-based synthesis of cinnamide analogues as anti-biofilm compounds against marine bacteria
[Display omitted] A set of triazole-based analogues of N-coumaroyltyramine was designed to discover potential leads that may help in the control of bacterial biofilms. the most potent compounds act as inhibitors of biofilm development with EC50 closed to ampicillin (EC50 = 11 μM) without toxic effec...
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Published in: | Bioorganic & medicinal chemistry letters 2018-01, Vol.28 (2), p.155-159 |
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container_title | Bioorganic & medicinal chemistry letters |
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creator | Sall, C. Ayé, M. Bottzeck, O. Praud, A. Blache, Y. |
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A set of triazole-based analogues of N-coumaroyltyramine was designed to discover potential leads that may help in the control of bacterial biofilms. the most potent compounds act as inhibitors of biofilm development with EC50 closed to ampicillin (EC50 = 11 μM) without toxic effect on bacterial growth even at high concentrations(100 μM). |
doi_str_mv | 10.1016/j.bmcl.2017.11.039 |
format | article |
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A set of triazole-based analogues of N-coumaroyltyramine was designed to discover potential leads that may help in the control of bacterial biofilms. the most potent compounds act as inhibitors of biofilm development with EC50 closed to ampicillin (EC50 = 11 μM) without toxic effect on bacterial growth even at high concentrations(100 μM).</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/j.bmcl.2017.11.039</identifier><identifier>PMID: 29198862</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>1,3 Cycloadditions ; Anti-biofilm ; Bacteria ; Chemical Sciences ; Click chemistry ; Material chemistry ; Polymers ; Triazole</subject><ispartof>Bioorganic & medicinal chemistry letters, 2018-01, Vol.28 (2), p.155-159</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-7cae37f0e0bcaf87f44d374ec07db8b30142dd99f70aa35416d666be7238e1c73</citedby><cites>FETCH-LOGICAL-c390t-7cae37f0e0bcaf87f44d374ec07db8b30142dd99f70aa35416d666be7238e1c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29198862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01878442$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sall, C.</creatorcontrib><creatorcontrib>Ayé, M.</creatorcontrib><creatorcontrib>Bottzeck, O.</creatorcontrib><creatorcontrib>Praud, A.</creatorcontrib><creatorcontrib>Blache, Y.</creatorcontrib><title>Towards smart biocide-free anti-biofilm strategies: Click-based synthesis of cinnamide analogues as anti-biofilm compounds against marine bacteria</title><title>Bioorganic & medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>[Display omitted]
A set of triazole-based analogues of N-coumaroyltyramine was designed to discover potential leads that may help in the control of bacterial biofilms. the most potent compounds act as inhibitors of biofilm development with EC50 closed to ampicillin (EC50 = 11 μM) without toxic effect on bacterial growth even at high concentrations(100 μM).</description><subject>1,3 Cycloadditions</subject><subject>Anti-biofilm</subject><subject>Bacteria</subject><subject>Chemical Sciences</subject><subject>Click chemistry</subject><subject>Material chemistry</subject><subject>Polymers</subject><subject>Triazole</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EokPLC7BA3rJIsGM3ThCbagQUaaRuitSddW1fTz0k8cj2FPU1eOJ6NFCJDasrXZ3v3J9DyDvOWs54_3HXmtlObce4ajlvmRhfkBWXvWyEZJcvyYqNPWuGUd6dkTc57xjjkkn5mpx1Ix-Hoe9W5Pdt_AXJZZpnSIWaEG1w2PiESGEpoakdH6aZ5pKg4DZg_kTXU7A_GwMZHc2PS7nHHDKNntqwLDBXg8rCFLcHzBTyv0Y2zvt4WOpI2EJYcqF1cliQGrAFU4AL8srDlPHtn3pOfnz9cru-bjY3376vrzaNFSMrjbKAQnmGzFjwg_JSOqEkWqacGYyox3bOjaNXDEBcSt67vu8Nqk4MyK0S5-TDyfceJr1Poa7xqCMEfX210cce44MapOweeNV2J61NMeeE_hngTB_D0Dt9DEMfw9Cc6xpGhd6foP3BzOiekb_fr4LPJwHWMx8CJp1twMWiCwlt0S6G__k_AaIOnlA</recordid><startdate>20180115</startdate><enddate>20180115</enddate><creator>Sall, C.</creator><creator>Ayé, M.</creator><creator>Bottzeck, O.</creator><creator>Praud, A.</creator><creator>Blache, Y.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope></search><sort><creationdate>20180115</creationdate><title>Towards smart biocide-free anti-biofilm strategies: Click-based synthesis of cinnamide analogues as anti-biofilm compounds against marine bacteria</title><author>Sall, C. ; Ayé, M. ; Bottzeck, O. ; Praud, A. ; Blache, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-7cae37f0e0bcaf87f44d374ec07db8b30142dd99f70aa35416d666be7238e1c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>1,3 Cycloadditions</topic><topic>Anti-biofilm</topic><topic>Bacteria</topic><topic>Chemical Sciences</topic><topic>Click chemistry</topic><topic>Material chemistry</topic><topic>Polymers</topic><topic>Triazole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sall, C.</creatorcontrib><creatorcontrib>Ayé, M.</creatorcontrib><creatorcontrib>Bottzeck, O.</creatorcontrib><creatorcontrib>Praud, A.</creatorcontrib><creatorcontrib>Blache, Y.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Bioorganic & medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sall, C.</au><au>Ayé, M.</au><au>Bottzeck, O.</au><au>Praud, A.</au><au>Blache, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards smart biocide-free anti-biofilm strategies: Click-based synthesis of cinnamide analogues as anti-biofilm compounds against marine bacteria</atitle><jtitle>Bioorganic & medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2018-01-15</date><risdate>2018</risdate><volume>28</volume><issue>2</issue><spage>155</spage><epage>159</epage><pages>155-159</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>[Display omitted]
A set of triazole-based analogues of N-coumaroyltyramine was designed to discover potential leads that may help in the control of bacterial biofilms. the most potent compounds act as inhibitors of biofilm development with EC50 closed to ampicillin (EC50 = 11 μM) without toxic effect on bacterial growth even at high concentrations(100 μM).</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>29198862</pmid><doi>10.1016/j.bmcl.2017.11.039</doi><tpages>5</tpages></addata></record> |
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source | ScienceDirect Freedom Collection |
subjects | 1,3 Cycloadditions Anti-biofilm Bacteria Chemical Sciences Click chemistry Material chemistry Polymers Triazole |
title | Towards smart biocide-free anti-biofilm strategies: Click-based synthesis of cinnamide analogues as anti-biofilm compounds against marine bacteria |
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