Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file
The human kinome comprises over 500 protein kinases. When mutated or over-expressed, many play critical roles in abnormal cellular functions associated with cancer, cardiovascular disease and neurological disorders. Here we report a step-economical approach to designed kinase inhibitors inspired by...
Gespeichert in:
Veröffentlicht in: | Organic chemistry frontiers an international journal of organic chemistry 2014-12, Vol.1 (10), p.1166-1171 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1171 |
---|---|
container_issue | 10 |
container_start_page | 1166 |
container_title | Organic chemistry frontiers an international journal of organic chemistry |
container_volume | 1 |
creator | Wender, Paul A Axtman, Alison D Golden, Jennifer E Kee, Jung-Min Sirois, Lauren E Quiroz, Ryan V Stevens, Matthew C |
description | The human kinome comprises over 500 protein kinases. When mutated or over-expressed, many play critical roles in abnormal cellular functions associated with cancer, cardiovascular disease and neurological disorders. Here we report a step-economical approach to designed kinase inhibitors inspired by the potent, but non-selective, natural product staurosporine, and synthetically enabled by a novel, complexity-increasing, serialized [5 + 2]/[4 + 2] cycloaddition strategy. This function-oriented synthesis approach rapidly affords tunable scaffolds, and produced a low nanomolar inhibitor of protein kinase C. |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1826607402</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1826607402</sourcerecordid><originalsourceid>FETCH-LOGICAL-p567-fbf2fc189f16ea2e385eb3caa9607a445ebc334330e7f80ad6499063e807801f3</originalsourceid><addsrcrecordid>eNp1UsFu2zAMzYYNa9H1FwYeO6DOZMuxnd6GNN0CdOghvQe0TNdaZcuV5Gy99VO2n9mH9EtGJymwyw6ERPLx8ZHg68lxImZJlMaxePPP_2hy6v13IUSczDIxy99NjvgjE5nmx6_-XA2dCtp2EBpnh7sGSm0j3fleO6rOwT92oSGvPcdq61qqoGL3rrsAH6iPSNnOtlqheYGSB1sfQIy-1x16At01utTBOv_89OuSKq4InA0WvuFPNoPKaTwHhNpp6ipANq8aa9DBj8YyhVecULTLKEcY9JaA2weny2EcwY90_1GlPTS4HXXsJ4PBAxqzI2vtdpTSENSaDJMbbudGsjGmK0IzfX76vTSkgrOdVuCHvjfUUhfQPcJ-M7jb4tlyvfoIuEVtsDR0Aetd_8BFvbOKqsHxgnbD9SMdK6ww4BTWRHB5s7qAWExjIeefVPpghUiSolkYre6hIccCrQOsKj32OpSyaEPvJ29rNJ5OD-_J5PZqebv4Gl3ffFktPl9H_SzLo7qsk1rFxbyOM8KEZDGjUirEeSZyTFP2lJSplILyuhBYZel8LjJJhcgLEdfyZHK2p-VZHgbyYdNqr8gY7MgOfhMXScZUqUgY-uEAHUq-mk3vdMvL2rycnvwL26Ljsw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1826607402</pqid></control><display><type>article</type><title>Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Wender, Paul A ; Axtman, Alison D ; Golden, Jennifer E ; Kee, Jung-Min ; Sirois, Lauren E ; Quiroz, Ryan V ; Stevens, Matthew C</creator><creatorcontrib>Wender, Paul A ; Axtman, Alison D ; Golden, Jennifer E ; Kee, Jung-Min ; Sirois, Lauren E ; Quiroz, Ryan V ; Stevens, Matthew C</creatorcontrib><description>The human kinome comprises over 500 protein kinases. When mutated or over-expressed, many play critical roles in abnormal cellular functions associated with cancer, cardiovascular disease and neurological disorders. Here we report a step-economical approach to designed kinase inhibitors inspired by the potent, but non-selective, natural product staurosporine, and synthetically enabled by a novel, complexity-increasing, serialized [5 + 2]/[4 + 2] cycloaddition strategy. This function-oriented synthesis approach rapidly affords tunable scaffolds, and produced a low nanomolar inhibitor of protein kinase C.</description><identifier>ISSN: 2052-4110</identifier><identifier>EISSN: 2052-4110</identifier><identifier>PMID: 25632347</identifier><language>eng</language><publisher>England</publisher><ispartof>Organic chemistry frontiers an international journal of organic chemistry, 2014-12, Vol.1 (10), p.1166-1171</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25632347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wender, Paul A</creatorcontrib><creatorcontrib>Axtman, Alison D</creatorcontrib><creatorcontrib>Golden, Jennifer E</creatorcontrib><creatorcontrib>Kee, Jung-Min</creatorcontrib><creatorcontrib>Sirois, Lauren E</creatorcontrib><creatorcontrib>Quiroz, Ryan V</creatorcontrib><creatorcontrib>Stevens, Matthew C</creatorcontrib><title>Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file</title><title>Organic chemistry frontiers an international journal of organic chemistry</title><addtitle>Org Chem Front</addtitle><description>The human kinome comprises over 500 protein kinases. When mutated or over-expressed, many play critical roles in abnormal cellular functions associated with cancer, cardiovascular disease and neurological disorders. Here we report a step-economical approach to designed kinase inhibitors inspired by the potent, but non-selective, natural product staurosporine, and synthetically enabled by a novel, complexity-increasing, serialized [5 + 2]/[4 + 2] cycloaddition strategy. This function-oriented synthesis approach rapidly affords tunable scaffolds, and produced a low nanomolar inhibitor of protein kinase C.</description><issn>2052-4110</issn><issn>2052-4110</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1UsFu2zAMzYYNa9H1FwYeO6DOZMuxnd6GNN0CdOghvQe0TNdaZcuV5Gy99VO2n9mH9EtGJymwyw6ERPLx8ZHg68lxImZJlMaxePPP_2hy6v13IUSczDIxy99NjvgjE5nmx6_-XA2dCtp2EBpnh7sGSm0j3fleO6rOwT92oSGvPcdq61qqoGL3rrsAH6iPSNnOtlqheYGSB1sfQIy-1x16At01utTBOv_89OuSKq4InA0WvuFPNoPKaTwHhNpp6ipANq8aa9DBj8YyhVecULTLKEcY9JaA2weny2EcwY90_1GlPTS4HXXsJ4PBAxqzI2vtdpTSENSaDJMbbudGsjGmK0IzfX76vTSkgrOdVuCHvjfUUhfQPcJ-M7jb4tlyvfoIuEVtsDR0Aetd_8BFvbOKqsHxgnbD9SMdK6ww4BTWRHB5s7qAWExjIeefVPpghUiSolkYre6hIccCrQOsKj32OpSyaEPvJ29rNJ5OD-_J5PZqebv4Gl3ffFktPl9H_SzLo7qsk1rFxbyOM8KEZDGjUirEeSZyTFP2lJSplILyuhBYZel8LjJJhcgLEdfyZHK2p-VZHgbyYdNqr8gY7MgOfhMXScZUqUgY-uEAHUq-mk3vdMvL2rycnvwL26Ljsw</recordid><startdate>20141229</startdate><enddate>20141229</enddate><creator>Wender, Paul A</creator><creator>Axtman, Alison D</creator><creator>Golden, Jennifer E</creator><creator>Kee, Jung-Min</creator><creator>Sirois, Lauren E</creator><creator>Quiroz, Ryan V</creator><creator>Stevens, Matthew C</creator><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20141229</creationdate><title>Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file</title><author>Wender, Paul A ; Axtman, Alison D ; Golden, Jennifer E ; Kee, Jung-Min ; Sirois, Lauren E ; Quiroz, Ryan V ; Stevens, Matthew C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p567-fbf2fc189f16ea2e385eb3caa9607a445ebc334330e7f80ad6499063e807801f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wender, Paul A</creatorcontrib><creatorcontrib>Axtman, Alison D</creatorcontrib><creatorcontrib>Golden, Jennifer E</creatorcontrib><creatorcontrib>Kee, Jung-Min</creatorcontrib><creatorcontrib>Sirois, Lauren E</creatorcontrib><creatorcontrib>Quiroz, Ryan V</creatorcontrib><creatorcontrib>Stevens, Matthew C</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Organic chemistry frontiers an international journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wender, Paul A</au><au>Axtman, Alison D</au><au>Golden, Jennifer E</au><au>Kee, Jung-Min</au><au>Sirois, Lauren E</au><au>Quiroz, Ryan V</au><au>Stevens, Matthew C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file</atitle><jtitle>Organic chemistry frontiers an international journal of organic chemistry</jtitle><addtitle>Org Chem Front</addtitle><date>2014-12-29</date><risdate>2014</risdate><volume>1</volume><issue>10</issue><spage>1166</spage><epage>1171</epage><pages>1166-1171</pages><issn>2052-4110</issn><eissn>2052-4110</eissn><abstract>The human kinome comprises over 500 protein kinases. When mutated or over-expressed, many play critical roles in abnormal cellular functions associated with cancer, cardiovascular disease and neurological disorders. Here we report a step-economical approach to designed kinase inhibitors inspired by the potent, but non-selective, natural product staurosporine, and synthetically enabled by a novel, complexity-increasing, serialized [5 + 2]/[4 + 2] cycloaddition strategy. This function-oriented synthesis approach rapidly affords tunable scaffolds, and produced a low nanomolar inhibitor of protein kinase C.</abstract><cop>England</cop><pmid>25632347</pmid><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2052-4110 |
ispartof | Organic chemistry frontiers an international journal of organic chemistry, 2014-12, Vol.1 (10), p.1166-1171 |
issn | 2052-4110 2052-4110 |
language | eng |
recordid | cdi_proquest_miscellaneous_1826607402 |
source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Function through bio-inspired, synthesis-informed design: step-economical syntheses of designed kinase inhibitors†Dedicated to Max Malacria, a friend and scholar whose science and creative contributions to step-economical synthesis have inspired us all and moved the field closer to the ideal.‡Electronic supplementary information (ESI) available: Synthetic procedures and spectral data. See DOI: 10.1039/c4qo00228hClick here for additional data file |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T22%3A52%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Function%20through%20bio-inspired,%20synthesis-informed%20design:%20step-economical%20syntheses%20of%20designed%20kinase%20inhibitors%E2%80%A0Dedicated%20to%20Max%20Malacria,%20a%20friend%20and%20scholar%20whose%20science%20and%20creative%20contributions%20to%20step-economical%20synthesis%20have%20inspired%20us%20all%20and%20moved%20the%20field%20closer%20to%20the%20ideal.%E2%80%A1Electronic%20supplementary%20information%20(ESI)%20available:%20Synthetic%20procedures%20and%20spectral%20data.%20See%20DOI:%2010.1039/c4qo00228hClick%20here%20for%20additional%20data%20file&rft.jtitle=Organic%20chemistry%20frontiers%20an%20international%20journal%20of%20organic%20chemistry&rft.au=Wender,%20Paul%20A&rft.date=2014-12-29&rft.volume=1&rft.issue=10&rft.spage=1166&rft.epage=1171&rft.pages=1166-1171&rft.issn=2052-4110&rft.eissn=2052-4110&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E1826607402%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1826607402&rft_id=info:pmid/25632347&rfr_iscdi=true |