Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones

6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against fungi. Many of these tested compounds exhibited potent antifungal activity. 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against two pathog...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bioorganic & medicinal chemistry letters 2011-01, Vol.21 (1), p.427-430
Hauptverfasser: Ryu, Chung-Kyu, Lee, Seung-Yon, Kim, Na Young, Hong, Jung An, Yoon, Joo Hee, Kim, Aram
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 430
container_issue 1
container_start_page 427
container_title Bioorganic & medicinal chemistry letters
container_volume 21
creator Ryu, Chung-Kyu
Lee, Seung-Yon
Kim, Na Young
Hong, Jung An
Yoon, Joo Hee
Kim, Aram
description 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against fungi. Many of these tested compounds exhibited potent antifungal activity. 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among them tested, many compounds showed good antifungal activity. The results suggest that 6-hydroxy-1H-carbazole-1,4(9H)-diones would be potent antifungal agents.
doi_str_mv 10.1016/j.bmcl.2010.10.124
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_883028931</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0960894X10015854</els_id><sourcerecordid>821198249</sourcerecordid><originalsourceid>FETCH-LOGICAL-c507t-a3d0bf07e8a04bf750fe1c3ec4c4a3d4c3c12a9113500335274d16df840b4a683</originalsourceid><addsrcrecordid>eNqF0E1vEzEQBmALUdFQ-AMcIBdUKuEwY89-SVyqChqkSBxKJW6W1x-to81usXcrwq_HaVK4wcGyNH5mbL-MvUJYIGD5Yb1oN6ZbCHgoLFDQEzZDKolLguIpm0FTAq8b-n7Mnqe0BkAComfsWCBURSmLGVtdbfvx1qWQ5rq3eY3BT_2N7ubuXneTHsPQzwc_L_nt1sbh55bjkhsdW_1r6BzH9_SuWZ5xm5lLL9iR111yLw_7Cbv-_OnbxZKvvl5-uThfcVNANXItLbQeKldroNZXBXiHRjpDhvIZGWlQ6AZRFgBSFqIii6X1NUFLuqzlCTvdz72Lw4_JpVFtQjKu63TvhimpupYg6kbi_6VAbGpBTZZiL00cUorOq7sYNjpuFYLaxa3Wahe32sX9UBOUm14fxk_txtk_LY_5ZvD2AHQyuvNR9yakv05WIv9HZPdm77welL6J2Vxf5ZtyAChJVDvxcS9cDvY-uKiSCa43zobozKjsEP710t-pkaSH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>821198249</pqid></control><display><type>article</type><title>Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Ryu, Chung-Kyu ; Lee, Seung-Yon ; Kim, Na Young ; Hong, Jung An ; Yoon, Joo Hee ; Kim, Aram</creator><creatorcontrib>Ryu, Chung-Kyu ; Lee, Seung-Yon ; Kim, Na Young ; Hong, Jung An ; Yoon, Joo Hee ; Kim, Aram</creatorcontrib><description>6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against fungi. Many of these tested compounds exhibited potent antifungal activity. 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among them tested, many compounds showed good antifungal activity. The results suggest that 6-hydroxy-1H-carbazole-1,4(9H)-diones would be potent antifungal agents.</description><identifier>ISSN: 0960-894X</identifier><identifier>EISSN: 1464-3405</identifier><identifier>DOI: 10.1016/j.bmcl.2010.10.124</identifier><identifier>PMID: 21075635</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>6-Hydroxy-1H-carbazole-1,4(9H)-diones ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal ; Antifungal agents ; Antifungal Agents - chemical synthesis ; Antifungal Agents - chemistry ; Antifungal Agents - pharmacology ; antifungal properties ; Antimicrobial compounds ; Biological and medical sciences ; Carbazoles - chemical synthesis ; Carbazoles - chemistry ; Carbazoles - pharmacology ; chemistry ; Fungi ; Fungi - drug effects ; Medical sciences ; Microbial Sensitivity Tests ; Pharmacology. Drug treatments ; Structure-Activity Relationship ; Substitution effects ; virulent strains</subject><ispartof>Bioorganic &amp; medicinal chemistry letters, 2011-01, Vol.21 (1), p.427-430</ispartof><rights>2010 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-a3d0bf07e8a04bf750fe1c3ec4c4a3d4c3c12a9113500335274d16df840b4a683</citedby><cites>FETCH-LOGICAL-c507t-a3d0bf07e8a04bf750fe1c3ec4c4a3d4c3c12a9113500335274d16df840b4a683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bmcl.2010.10.124$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23726832$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21075635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ryu, Chung-Kyu</creatorcontrib><creatorcontrib>Lee, Seung-Yon</creatorcontrib><creatorcontrib>Kim, Na Young</creatorcontrib><creatorcontrib>Hong, Jung An</creatorcontrib><creatorcontrib>Yoon, Joo Hee</creatorcontrib><creatorcontrib>Kim, Aram</creatorcontrib><title>Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones</title><title>Bioorganic &amp; medicinal chemistry letters</title><addtitle>Bioorg Med Chem Lett</addtitle><description>6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against fungi. Many of these tested compounds exhibited potent antifungal activity. 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among them tested, many compounds showed good antifungal activity. The results suggest that 6-hydroxy-1H-carbazole-1,4(9H)-diones would be potent antifungal agents.</description><subject>6-Hydroxy-1H-carbazole-1,4(9H)-diones</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal</subject><subject>Antifungal agents</subject><subject>Antifungal Agents - chemical synthesis</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - pharmacology</subject><subject>antifungal properties</subject><subject>Antimicrobial compounds</subject><subject>Biological and medical sciences</subject><subject>Carbazoles - chemical synthesis</subject><subject>Carbazoles - chemistry</subject><subject>Carbazoles - pharmacology</subject><subject>chemistry</subject><subject>Fungi</subject><subject>Fungi - drug effects</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>Pharmacology. Drug treatments</subject><subject>Structure-Activity Relationship</subject><subject>Substitution effects</subject><subject>virulent strains</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1vEzEQBmALUdFQ-AMcIBdUKuEwY89-SVyqChqkSBxKJW6W1x-to81usXcrwq_HaVK4wcGyNH5mbL-MvUJYIGD5Yb1oN6ZbCHgoLFDQEzZDKolLguIpm0FTAq8b-n7Mnqe0BkAComfsWCBURSmLGVtdbfvx1qWQ5rq3eY3BT_2N7ubuXneTHsPQzwc_L_nt1sbh55bjkhsdW_1r6BzH9_SuWZ5xm5lLL9iR111yLw_7Cbv-_OnbxZKvvl5-uThfcVNANXItLbQeKldroNZXBXiHRjpDhvIZGWlQ6AZRFgBSFqIii6X1NUFLuqzlCTvdz72Lw4_JpVFtQjKu63TvhimpupYg6kbi_6VAbGpBTZZiL00cUorOq7sYNjpuFYLaxa3Wahe32sX9UBOUm14fxk_txtk_LY_5ZvD2AHQyuvNR9yakv05WIv9HZPdm77welL6J2Vxf5ZtyAChJVDvxcS9cDvY-uKiSCa43zobozKjsEP710t-pkaSH</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Ryu, Chung-Kyu</creator><creator>Lee, Seung-Yon</creator><creator>Kim, Na Young</creator><creator>Hong, Jung An</creator><creator>Yoon, Joo Hee</creator><creator>Kim, Aram</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</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>7X8</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20110101</creationdate><title>Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones</title><author>Ryu, Chung-Kyu ; Lee, Seung-Yon ; Kim, Na Young ; Hong, Jung An ; Yoon, Joo Hee ; Kim, Aram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-a3d0bf07e8a04bf750fe1c3ec4c4a3d4c3c12a9113500335274d16df840b4a683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>6-Hydroxy-1H-carbazole-1,4(9H)-diones</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal</topic><topic>Antifungal agents</topic><topic>Antifungal Agents - chemical synthesis</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - pharmacology</topic><topic>antifungal properties</topic><topic>Antimicrobial compounds</topic><topic>Biological and medical sciences</topic><topic>Carbazoles - chemical synthesis</topic><topic>Carbazoles - chemistry</topic><topic>Carbazoles - pharmacology</topic><topic>chemistry</topic><topic>Fungi</topic><topic>Fungi - drug effects</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Pharmacology. Drug treatments</topic><topic>Structure-Activity Relationship</topic><topic>Substitution effects</topic><topic>virulent strains</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ryu, Chung-Kyu</creatorcontrib><creatorcontrib>Lee, Seung-Yon</creatorcontrib><creatorcontrib>Kim, Na Young</creatorcontrib><creatorcontrib>Hong, Jung An</creatorcontrib><creatorcontrib>Yoon, Joo Hee</creatorcontrib><creatorcontrib>Kim, Aram</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Bioorganic &amp; medicinal chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ryu, Chung-Kyu</au><au>Lee, Seung-Yon</au><au>Kim, Na Young</au><au>Hong, Jung An</au><au>Yoon, Joo Hee</au><au>Kim, Aram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones</atitle><jtitle>Bioorganic &amp; medicinal chemistry letters</jtitle><addtitle>Bioorg Med Chem Lett</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>21</volume><issue>1</issue><spage>427</spage><epage>430</epage><pages>427-430</pages><issn>0960-894X</issn><eissn>1464-3405</eissn><abstract>6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against fungi. Many of these tested compounds exhibited potent antifungal activity. 6-Hydroxy-1H-carbazole-1,4(9H)-diones were synthesized and tested for in vitro antifungal activity against two pathogenic strains of fungi. Among them tested, many compounds showed good antifungal activity. The results suggest that 6-hydroxy-1H-carbazole-1,4(9H)-diones would be potent antifungal agents.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>21075635</pmid><doi>10.1016/j.bmcl.2010.10.124</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0960-894X
ispartof Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (1), p.427-430
issn 0960-894X
1464-3405
language eng
recordid cdi_proquest_miscellaneous_883028931
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects 6-Hydroxy-1H-carbazole-1,4(9H)-diones
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antifungal
Antifungal agents
Antifungal Agents - chemical synthesis
Antifungal Agents - chemistry
Antifungal Agents - pharmacology
antifungal properties
Antimicrobial compounds
Biological and medical sciences
Carbazoles - chemical synthesis
Carbazoles - chemistry
Carbazoles - pharmacology
chemistry
Fungi
Fungi - drug effects
Medical sciences
Microbial Sensitivity Tests
Pharmacology. Drug treatments
Structure-Activity Relationship
Substitution effects
virulent strains
title Synthesis and antifungal evaluation of 6-hydroxy-1H-carbazole-1,4(9H)-diones
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T07%3A32%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20antifungal%20evaluation%20of%206-hydroxy-1H-carbazole-1,4(9H)-diones&rft.jtitle=Bioorganic%20&%20medicinal%20chemistry%20letters&rft.au=Ryu,%20Chung-Kyu&rft.date=2011-01-01&rft.volume=21&rft.issue=1&rft.spage=427&rft.epage=430&rft.pages=427-430&rft.issn=0960-894X&rft.eissn=1464-3405&rft_id=info:doi/10.1016/j.bmcl.2010.10.124&rft_dat=%3Cproquest_cross%3E821198249%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=821198249&rft_id=info:pmid/21075635&rft_els_id=S0960894X10015854&rfr_iscdi=true