Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions
2-Pyridone-containing heterocycles are considered privileged scaffolds in drug discovery due to their behavior as hydrogen bond donors and/or acceptors and nonpeptidic mimics, and remarkable physicochemical properties such as metabolic stability, solubility in water, and lipophilicity. This review p...
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Veröffentlicht in: | RSC advances 2022-12, Vol.12 (54), p.34965-34983 |
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creator | Hurtado-Rodríguez, Diana Salinas-Torres, Angélica Rojas, Hugo Becerra, Diana Castillo, Juan-Carlos |
description | 2-Pyridone-containing heterocycles are considered privileged scaffolds in drug discovery due to their behavior as hydrogen bond donors and/or acceptors and nonpeptidic mimics, and remarkable physicochemical properties such as metabolic stability, solubility in water, and lipophilicity. This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of 2-pyridone-containing heterocycles. In particular, it covers the articles published from 1999 to date related to anticancer, antibacterial, antifungal, anti-inflammatory, α-glucosidase inhibitor, and cardiotonic activities of 2-pyridone-containing heterocycles obtained exclusively by an MCR. The discussion focuses on bioactivity data, synthetic approaches, plausible reaction mechanisms, and molecular docking simulations to facilitate comparison and underscore the applications of the 2-pyridone motif in drug discovery and medicinal chemistry. We also present our conclusions and outlook for the future.
This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of biologically active 2-pyridone-containing heterocycles. |
doi_str_mv | 10.1039/d2ra07056a |
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This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of biologically active 2-pyridone-containing heterocycles.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d2ra07056a</identifier><identifier>PMID: 36540221</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biological activity ; Chemical synthesis ; Chemistry ; Fungicides ; Glucosidase ; Hydrogen bonds ; Molecular docking ; Reaction mechanisms</subject><ispartof>RSC advances, 2022-12, Vol.12 (54), p.34965-34983</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2022</rights><rights>This journal is © The Royal Society of Chemistry 2022 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-c90482939146d3d2988eb41f4a22bb8c44b18104fe9b0a530a77370b4ee2ffd93</citedby><cites>FETCH-LOGICAL-c428t-c90482939146d3d2988eb41f4a22bb8c44b18104fe9b0a530a77370b4ee2ffd93</cites><orcidid>0000-0002-6060-2578</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727751/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727751/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36540221$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hurtado-Rodríguez, Diana</creatorcontrib><creatorcontrib>Salinas-Torres, Angélica</creatorcontrib><creatorcontrib>Rojas, Hugo</creatorcontrib><creatorcontrib>Becerra, Diana</creatorcontrib><creatorcontrib>Castillo, Juan-Carlos</creatorcontrib><title>Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>2-Pyridone-containing heterocycles are considered privileged scaffolds in drug discovery due to their behavior as hydrogen bond donors and/or acceptors and nonpeptidic mimics, and remarkable physicochemical properties such as metabolic stability, solubility in water, and lipophilicity. This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of 2-pyridone-containing heterocycles. In particular, it covers the articles published from 1999 to date related to anticancer, antibacterial, antifungal, anti-inflammatory, α-glucosidase inhibitor, and cardiotonic activities of 2-pyridone-containing heterocycles obtained exclusively by an MCR. The discussion focuses on bioactivity data, synthetic approaches, plausible reaction mechanisms, and molecular docking simulations to facilitate comparison and underscore the applications of the 2-pyridone motif in drug discovery and medicinal chemistry. We also present our conclusions and outlook for the future.
This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of biologically active 2-pyridone-containing heterocycles.</description><subject>Biological activity</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Fungicides</subject><subject>Glucosidase</subject><subject>Hydrogen bonds</subject><subject>Molecular docking</subject><subject>Reaction mechanisms</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkVFLHDEUhYO0VLG-9F0Z6EspTE1uMsnkRdjaVguCIPocMpk7bmQmWZMZYf99Z1272ublBs53D-dyCPnE6DdGuT5tIVmqaCXtHjkAKmQJVOp3b_775CjnBzo_WTGQ7APZ57ISFIAdkNvvPlo3-icsoFytk29jwNLFMFoffLgvljhiim7teizyOoxLzJiLKW-0YepH7-KwmnfCWCTcOMWQP5L3ne0zHr3MQ3L36-ft-WV5dX3x-3xxVToB9Vg6TUUNmmsmZMtb0HWNjWCdsABNUzshGlYzKjrUDbUVp1YprmgjEKHrWs0PydnWdzU1A7ZuDpFsb1bJDzatTbTe_KsEvzT38cloBUpVbDb48mKQ4uOEeTSDzw773gaMUzagKikVyGf083_oQ5xSmM_bUILXEgTM1Nct5VLMOWG3C8Oo2fRlfsDN4rmvxQyfvI2_Q_-2MwPHWyBlt1NfC-d_AFFVm18</recordid><startdate>20221206</startdate><enddate>20221206</enddate><creator>Hurtado-Rodríguez, Diana</creator><creator>Salinas-Torres, Angélica</creator><creator>Rojas, Hugo</creator><creator>Becerra, Diana</creator><creator>Castillo, Juan-Carlos</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6060-2578</orcidid></search><sort><creationdate>20221206</creationdate><title>Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions</title><author>Hurtado-Rodríguez, Diana ; Salinas-Torres, Angélica ; Rojas, Hugo ; Becerra, Diana ; Castillo, Juan-Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-c90482939146d3d2988eb41f4a22bb8c44b18104fe9b0a530a77370b4ee2ffd93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biological activity</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Fungicides</topic><topic>Glucosidase</topic><topic>Hydrogen bonds</topic><topic>Molecular docking</topic><topic>Reaction mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hurtado-Rodríguez, Diana</creatorcontrib><creatorcontrib>Salinas-Torres, Angélica</creatorcontrib><creatorcontrib>Rojas, Hugo</creatorcontrib><creatorcontrib>Becerra, Diana</creatorcontrib><creatorcontrib>Castillo, Juan-Carlos</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hurtado-Rodríguez, Diana</au><au>Salinas-Torres, Angélica</au><au>Rojas, Hugo</au><au>Becerra, Diana</au><au>Castillo, Juan-Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2022-12-06</date><risdate>2022</risdate><volume>12</volume><issue>54</issue><spage>34965</spage><epage>34983</epage><pages>34965-34983</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>2-Pyridone-containing heterocycles are considered privileged scaffolds in drug discovery due to their behavior as hydrogen bond donors and/or acceptors and nonpeptidic mimics, and remarkable physicochemical properties such as metabolic stability, solubility in water, and lipophilicity. This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of 2-pyridone-containing heterocycles. In particular, it covers the articles published from 1999 to date related to anticancer, antibacterial, antifungal, anti-inflammatory, α-glucosidase inhibitor, and cardiotonic activities of 2-pyridone-containing heterocycles obtained exclusively by an MCR. The discussion focuses on bioactivity data, synthetic approaches, plausible reaction mechanisms, and molecular docking simulations to facilitate comparison and underscore the applications of the 2-pyridone motif in drug discovery and medicinal chemistry. We also present our conclusions and outlook for the future.
This review provides a comprehensive overview of multicomponent reactions (MCRs) for the synthesis of biologically active 2-pyridone-containing heterocycles.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36540221</pmid><doi>10.1039/d2ra07056a</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-6060-2578</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biological activity Chemical synthesis Chemistry Fungicides Glucosidase Hydrogen bonds Molecular docking Reaction mechanisms |
title | Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions |
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