Synthesis of Isomeric, Oxathiolone Fused Chalcones, and Comparison of Their Activity toward Various Microorganisms and Human Cancer Cells Line
Isomeric oxathiolone fused chalcones were prepared by condensation of appropriate acetylbenzo[1,3]oxathiol-2-ones with benzaldehydes under acidic conditions. The synthesized compounds were screened for cytotoxic activity using HeLa cells, as well as for antibacterial activity against Micrococcus lut...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 2007, Vol.55(5), pp.817-820 |
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creator | Konieczny, Marek Tadeusz Konieczny, Wojciech Sabisz, Michał Skladanowski, Andrzej Wakieć, Roland Augustynowicz-Kopeć, Ewa Zwolska, Zofia |
description | Isomeric oxathiolone fused chalcones were prepared by condensation of appropriate acetylbenzo[1,3]oxathiol-2-ones with benzaldehydes under acidic conditions. The synthesized compounds were screened for cytotoxic activity using HeLa cells, as well as for antibacterial activity against Micrococcus luteus, Staphylococcus aureus, Salmonella typhimurium, Escherichia coli, Proteus vulgaris, antifungal activity against Candida albicans, and tuberculostatic activity against Mycobacterium tuberculosis H37Rv and Mycobacterium kansasii strains. |
doi_str_mv | 10.1248/cpb.55.817 |
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The synthesized compounds were screened for cytotoxic activity using HeLa cells, as well as for antibacterial activity against Micrococcus luteus, Staphylococcus aureus, Salmonella typhimurium, Escherichia coli, Proteus vulgaris, antifungal activity against Candida albicans, and tuberculostatic activity against Mycobacterium tuberculosis H37Rv and Mycobacterium kansasii strains.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.55.817</identifier><identifier>PMID: 17473478</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Anti-Infective Agents - chemical synthesis ; Anti-Infective Agents - pharmacology ; antibacterial ; antifungal ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - pharmacology ; Antitubercular Agents - chemical synthesis ; Antitubercular Agents - pharmacology ; Bridged Bicyclo Compounds, Heterocyclic - chemistry ; Bridged Bicyclo Compounds, Heterocyclic - pharmacology ; Candida albicans ; Cell Line, Tumor ; chalcone ; Chalcones - chemistry ; Chalcones - isolation & purification ; Chalcones - pharmacology ; cytostatic ; Drug Screening Assays, Antitumor ; Escherichia coli ; HeLa Cells ; Humans ; Isomerism ; Magnetic Resonance Spectroscopy ; Microbial Sensitivity Tests ; Micrococcus luteus ; Mycobacterium kansasii ; Mycobacterium tuberculosis ; oxathiolone ; Proteus vulgaris ; Salmonella typhimurium ; Staphylococcus aureus ; Tetrazolium Salts ; Thiazoles ; tuberculostatic</subject><ispartof>Chemical and Pharmaceutical Bulletin, 2007, Vol.55(5), pp.817-820</ispartof><rights>2007 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-768ad8270b6617c15574151af5a3050c0ed926d762b84486d4b1ad27e1dea4813</citedby><cites>FETCH-LOGICAL-c526t-768ad8270b6617c15574151af5a3050c0ed926d762b84486d4b1ad27e1dea4813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17473478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konieczny, Marek Tadeusz</creatorcontrib><creatorcontrib>Konieczny, Wojciech</creatorcontrib><creatorcontrib>Sabisz, Michał</creatorcontrib><creatorcontrib>Skladanowski, Andrzej</creatorcontrib><creatorcontrib>Wakieć, Roland</creatorcontrib><creatorcontrib>Augustynowicz-Kopeć, Ewa</creatorcontrib><creatorcontrib>Zwolska, Zofia</creatorcontrib><title>Synthesis of Isomeric, Oxathiolone Fused Chalcones, and Comparison of Their Activity toward Various Microorganisms and Human Cancer Cells Line</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>Isomeric oxathiolone fused chalcones were prepared by condensation of appropriate acetylbenzo[1,3]oxathiol-2-ones with benzaldehydes under acidic conditions. The synthesized compounds were screened for cytotoxic activity using HeLa cells, as well as for antibacterial activity against Micrococcus luteus, Staphylococcus aureus, Salmonella typhimurium, Escherichia coli, Proteus vulgaris, antifungal activity against Candida albicans, and tuberculostatic activity against Mycobacterium tuberculosis H37Rv and Mycobacterium kansasii strains.</description><subject>Anti-Infective Agents - chemical synthesis</subject><subject>Anti-Infective Agents - pharmacology</subject><subject>antibacterial</subject><subject>antifungal</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antitubercular Agents - chemical synthesis</subject><subject>Antitubercular Agents - pharmacology</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - chemistry</subject><subject>Bridged Bicyclo Compounds, Heterocyclic - pharmacology</subject><subject>Candida albicans</subject><subject>Cell Line, Tumor</subject><subject>chalcone</subject><subject>Chalcones - chemistry</subject><subject>Chalcones - isolation & purification</subject><subject>Chalcones - pharmacology</subject><subject>cytostatic</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Escherichia coli</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Isomerism</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Microbial Sensitivity Tests</subject><subject>Micrococcus luteus</subject><subject>Mycobacterium kansasii</subject><subject>Mycobacterium tuberculosis</subject><subject>oxathiolone</subject><subject>Proteus vulgaris</subject><subject>Salmonella typhimurium</subject><subject>Staphylococcus aureus</subject><subject>Tetrazolium Salts</subject><subject>Thiazoles</subject><subject>tuberculostatic</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQhy0EokvhwgMgS0gcULPYjv-kp6qKKK20qAcKV2vieBuvEnuxHWBfgmfGyy5U4sLF1sjffBrPD6GXlCwp4807s-2WQiwbqh6hBa25qgRj9WO0IIScV6yW9Ql6ltKGECaIqp-iE6q4KlyzQD8_7XwebHIJhzW-SWGy0ZkzfPsD8uDCGLzFV3OyPW4HGE0p0xkGX8owbSG6FPy-8W6wLuJLk903l3c4h-8Qe_ylAGFO-KMzMYR4D96lKf1uv54n8LgFb2zErR3HhFfO2-foyRrGZF8c71P0-er9XXtdrW4_3LSXq8oIJnOlZAN9wxTppKTKUCEUp4LCWkBNBDHE9udM9kqyruG8kT3vKPRMWdpb4A2tT9Gbg3cbw9fZpqwnl0wZA7wtE2tFuJCN4v8FWdkxlXxvfP0PuAlz9OUTmnJJOCm-ulBvD1RZSErRrvU2ugniTlOi92HqEqYWQpcwC_zqqJy7yfYP6DG9AlwcgE3KcG__AhCzM6P94xKHoygfXgaI2vr6F-h8sSo</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Konieczny, Marek Tadeusz</creator><creator>Konieczny, Wojciech</creator><creator>Sabisz, Michał</creator><creator>Skladanowski, Andrzej</creator><creator>Wakieć, Roland</creator><creator>Augustynowicz-Kopeć, Ewa</creator><creator>Zwolska, Zofia</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><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>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070501</creationdate><title>Synthesis of Isomeric, Oxathiolone Fused Chalcones, and Comparison of Their Activity toward Various Microorganisms and Human Cancer Cells Line</title><author>Konieczny, Marek Tadeusz ; Konieczny, Wojciech ; Sabisz, Michał ; Skladanowski, Andrzej ; Wakieć, Roland ; Augustynowicz-Kopeć, Ewa ; Zwolska, Zofia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-768ad8270b6617c15574151af5a3050c0ed926d762b84486d4b1ad27e1dea4813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Anti-Infective Agents - chemical synthesis</topic><topic>Anti-Infective Agents - pharmacology</topic><topic>antibacterial</topic><topic>antifungal</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antitubercular Agents - chemical synthesis</topic><topic>Antitubercular Agents - pharmacology</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - chemistry</topic><topic>Bridged Bicyclo Compounds, Heterocyclic - pharmacology</topic><topic>Candida albicans</topic><topic>Cell Line, Tumor</topic><topic>chalcone</topic><topic>Chalcones - chemistry</topic><topic>Chalcones - isolation & purification</topic><topic>Chalcones - pharmacology</topic><topic>cytostatic</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Escherichia coli</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Isomerism</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Microbial Sensitivity Tests</topic><topic>Micrococcus luteus</topic><topic>Mycobacterium kansasii</topic><topic>Mycobacterium tuberculosis</topic><topic>oxathiolone</topic><topic>Proteus vulgaris</topic><topic>Salmonella typhimurium</topic><topic>Staphylococcus aureus</topic><topic>Tetrazolium Salts</topic><topic>Thiazoles</topic><topic>tuberculostatic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konieczny, Marek Tadeusz</creatorcontrib><creatorcontrib>Konieczny, Wojciech</creatorcontrib><creatorcontrib>Sabisz, Michał</creatorcontrib><creatorcontrib>Skladanowski, Andrzej</creatorcontrib><creatorcontrib>Wakieć, Roland</creatorcontrib><creatorcontrib>Augustynowicz-Kopeć, Ewa</creatorcontrib><creatorcontrib>Zwolska, Zofia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</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><collection>MEDLINE - Academic</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konieczny, Marek Tadeusz</au><au>Konieczny, Wojciech</au><au>Sabisz, Michał</au><au>Skladanowski, Andrzej</au><au>Wakieć, Roland</au><au>Augustynowicz-Kopeć, Ewa</au><au>Zwolska, Zofia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Isomeric, Oxathiolone Fused Chalcones, and Comparison of Their Activity toward Various Microorganisms and Human Cancer Cells Line</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>55</volume><issue>5</issue><spage>817</spage><epage>820</epage><pages>817-820</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>Isomeric oxathiolone fused chalcones were prepared by condensation of appropriate acetylbenzo[1,3]oxathiol-2-ones with benzaldehydes under acidic conditions. The synthesized compounds were screened for cytotoxic activity using HeLa cells, as well as for antibacterial activity against Micrococcus luteus, Staphylococcus aureus, Salmonella typhimurium, Escherichia coli, Proteus vulgaris, antifungal activity against Candida albicans, and tuberculostatic activity against Mycobacterium tuberculosis H37Rv and Mycobacterium kansasii strains.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>17473478</pmid><doi>10.1248/cpb.55.817</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Infective Agents - chemical synthesis Anti-Infective Agents - pharmacology antibacterial antifungal Antineoplastic Agents - chemical synthesis Antineoplastic Agents - pharmacology Antitubercular Agents - chemical synthesis Antitubercular Agents - pharmacology Bridged Bicyclo Compounds, Heterocyclic - chemistry Bridged Bicyclo Compounds, Heterocyclic - pharmacology Candida albicans Cell Line, Tumor chalcone Chalcones - chemistry Chalcones - isolation & purification Chalcones - pharmacology cytostatic Drug Screening Assays, Antitumor Escherichia coli HeLa Cells Humans Isomerism Magnetic Resonance Spectroscopy Microbial Sensitivity Tests Micrococcus luteus Mycobacterium kansasii Mycobacterium tuberculosis oxathiolone Proteus vulgaris Salmonella typhimurium Staphylococcus aureus Tetrazolium Salts Thiazoles tuberculostatic |
title | Synthesis of Isomeric, Oxathiolone Fused Chalcones, and Comparison of Their Activity toward Various Microorganisms and Human Cancer Cells Line |
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