Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity
A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high...
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Veröffentlicht in: | Journal of enzyme inhibition and medicinal chemistry 2023-12, Vol.38 (1), p.2202362-2202362 |
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creator | Li, Xianru Li, Liping Zhang, Haonan Chi, Xiaochen Jiang, Yuanying Ni, Tingjunhong |
description | A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC
50
value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation. |
doi_str_mv | 10.1080/14756366.2023.2202362 |
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50
value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation.</description><identifier>ISSN: 1475-6366</identifier><identifier>EISSN: 1475-6374</identifier><identifier>DOI: 10.1080/14756366.2023.2202362</identifier><identifier>PMID: 37080774</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>antifungal ; Antifungal activity ; Antifungal agents ; Antifungal Agents - pharmacology ; Candida glabrata ; Cytotoxicity ; Drug resistance ; Fungal infections ; Fungi ; Hospitals ; Hydroxy-phenylhydrazone ; Medicine ; Microbial Sensitivity Tests ; Minimum inhibitory concentration ; Pathogens ; Pharmacy ; Research Paper ; structure-activity relationship ; synthesis ; thiosemicarbazone</subject><ispartof>Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2202362-2202362</ispartof><rights>2023 Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University. Published by Informa UK Limited, trading as Taylor & Francis Group 2023</rights><rights>2023 Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University. Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University. Published by Informa UK Limited, trading as Taylor & Francis Group 2023 Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-3a4f405929dd28f3c7b91b754c1050baffbdb3a4ecf81cc19eca95bc012801be3</citedby><cites>FETCH-LOGICAL-c563t-3a4f405929dd28f3c7b91b754c1050baffbdb3a4ecf81cc19eca95bc012801be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120463/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120463/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,27479,27901,27902,53766,53768,59116,59117</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37080774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Xianru</creatorcontrib><creatorcontrib>Li, Liping</creatorcontrib><creatorcontrib>Zhang, Haonan</creatorcontrib><creatorcontrib>Chi, Xiaochen</creatorcontrib><creatorcontrib>Jiang, Yuanying</creatorcontrib><creatorcontrib>Ni, Tingjunhong</creatorcontrib><title>Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity</title><title>Journal of enzyme inhibition and medicinal chemistry</title><addtitle>J Enzyme Inhib Med Chem</addtitle><description>A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC
50
value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation.</description><subject>antifungal</subject><subject>Antifungal activity</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - pharmacology</subject><subject>Candida glabrata</subject><subject>Cytotoxicity</subject><subject>Drug resistance</subject><subject>Fungal infections</subject><subject>Fungi</subject><subject>Hospitals</subject><subject>Hydroxy-phenylhydrazone</subject><subject>Medicine</subject><subject>Microbial Sensitivity Tests</subject><subject>Minimum inhibitory concentration</subject><subject>Pathogens</subject><subject>Pharmacy</subject><subject>Research Paper</subject><subject>structure-activity relationship</subject><subject>synthesis</subject><subject>thiosemicarbazone</subject><issn>1475-6366</issn><issn>1475-6374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNp9UsuOEzEQHCEQuwQ-AWSJC5cEv505AQqvlVbiAmerx4_E0cw42E5W4evxkGzEcuBit7ury92lapqXBC8IXuK3hCshmZQLiilb0OmU9FFzPeXnkin--BJLedU8y3mLMSWU8KfNFVOVQil-3YSPIZt4cOmIokdjjXpUNiFmNwQDqYNfcXTIuhQOUMLBZXQXygbtYnFjQTBalF3vzFSqrxLmq5oLFtC6hy5BAQRTMZTj8-aJhz67F-d71vz4_On76uv89tuXm9WH27mp-5Q5A-45Fi1traVLz4zqWtIpwQ3BAnfgfWe7CnLGL4kxpHUGWtEZTOgSk86xWXNz4rURtnqXwgDpqCME_ScR01pDKsH0ThvmvAGisBCcS9mCss5wDsK2mBliKte7E9du3w3Omrpzgv4B6cPKGDZ6HQ-a1HEwl6wyvDkzpPhz73LRQxXc9T2MLu6zrkMLTBUhbYW-_ge6jfs0Vq00bYkSAsuq0KwRJ5RJMefk_GUagvXkDH3vDD15Qp-dUfte_b3KpeveChXw_gQIo49pgLuYeqsLHPuYfILRhKzZ___4DZ4Xyow</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Li, Xianru</creator><creator>Li, Liping</creator><creator>Zhang, Haonan</creator><creator>Chi, Xiaochen</creator><creator>Jiang, Yuanying</creator><creator>Ni, Tingjunhong</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>202312</creationdate><title>Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity</title><author>Li, Xianru ; Li, Liping ; Zhang, Haonan ; Chi, Xiaochen ; Jiang, Yuanying ; Ni, Tingjunhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-3a4f405929dd28f3c7b91b754c1050baffbdb3a4ecf81cc19eca95bc012801be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>antifungal</topic><topic>Antifungal activity</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - pharmacology</topic><topic>Candida glabrata</topic><topic>Cytotoxicity</topic><topic>Drug resistance</topic><topic>Fungal infections</topic><topic>Fungi</topic><topic>Hospitals</topic><topic>Hydroxy-phenylhydrazone</topic><topic>Medicine</topic><topic>Microbial Sensitivity Tests</topic><topic>Minimum inhibitory concentration</topic><topic>Pathogens</topic><topic>Pharmacy</topic><topic>Research Paper</topic><topic>structure-activity relationship</topic><topic>synthesis</topic><topic>thiosemicarbazone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Xianru</creatorcontrib><creatorcontrib>Li, Liping</creatorcontrib><creatorcontrib>Zhang, Haonan</creatorcontrib><creatorcontrib>Chi, Xiaochen</creatorcontrib><creatorcontrib>Jiang, Yuanying</creatorcontrib><creatorcontrib>Ni, Tingjunhong</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of enzyme inhibition and medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Xianru</au><au>Li, Liping</au><au>Zhang, Haonan</au><au>Chi, Xiaochen</au><au>Jiang, Yuanying</au><au>Ni, Tingjunhong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity</atitle><jtitle>Journal of enzyme inhibition and medicinal chemistry</jtitle><addtitle>J Enzyme Inhib Med Chem</addtitle><date>2023-12</date><risdate>2023</risdate><volume>38</volume><issue>1</issue><spage>2202362</spage><epage>2202362</epage><pages>2202362-2202362</pages><issn>1475-6366</issn><eissn>1475-6374</eissn><abstract>A series of 21 novel compounds containing a thiosemicarbazone moiety were designed and synthesised based on hit compound 1 from our in-house compound library screening. Most compounds showed potent antifungal activity in vitro against seven common pathogenic fungi. Notably, all compounds showed high potency against Candida glabrata 537 (MIC = ≤0.0156-2 µg/mL). Of note, compounds 5j and 5r displayed excellent antifungal activity against Candida krusei 4946 and Candida auris 922. Additionally, compounds 5j and 5r also showed high potency against 15 C. glabrata isolates with MIC values ranging from 0.0625 µg/mL to 4 µg/mL, with compound 5r being slightly superior to 5j. Moreover, compound 5r has certain effect against biofilm formation of C. glabrata. Furthermore, compound 5r has minimal cytotoxicity against HUVECs with an IC
50
value of 15.89 µg/mL and no haemolysis at 64 µg/mL. Taken together, these results suggest that promising lead compound 5r deserves further investigation.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>37080774</pmid><doi>10.1080/14756366.2023.2202362</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antifungal Antifungal activity Antifungal agents Antifungal Agents - pharmacology Candida glabrata Cytotoxicity Drug resistance Fungal infections Fungi Hospitals Hydroxy-phenylhydrazone Medicine Microbial Sensitivity Tests Minimum inhibitory concentration Pathogens Pharmacy Research Paper structure-activity relationship synthesis thiosemicarbazone |
title | Discovery of novel thiosemicarbazone derivatives with potent and selective anti-Candida glabrata activity |
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