Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras

In this study, stereoisomeric aspergillide A/neopeltolide chimeras were synthesized in a parallel manner, and their antiproliferative activity was evaluated to demonstrate the potential utility of the 14-membered macrolactone structure embedded with a tetrahydropyran substructure as a template for d...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chemistry letters 2013, Vol.42 (9), p.1020-1022
Hauptverfasser: Fuwa, Haruhiko, Noto, Kenkichi, Kawakami, Masato, Sasaki, Makoto
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1022
container_issue 9
container_start_page 1020
container_title Chemistry letters
container_volume 42
creator Fuwa, Haruhiko
Noto, Kenkichi
Kawakami, Masato
Sasaki, Makoto
description In this study, stereoisomeric aspergillide A/neopeltolide chimeras were synthesized in a parallel manner, and their antiproliferative activity was evaluated to demonstrate the potential utility of the 14-membered macrolactone structure embedded with a tetrahydropyran substructure as a template for developing natural product-like antiproliferative agents.
doi_str_mv 10.1246/cl.130322
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1744677078</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1744677078</sourcerecordid><originalsourceid>FETCH-LOGICAL-c480t-859e96de2cc3d48f587ef6d3ac9a46f022ee2f2e8c3cee917b5d01398e4840973</originalsourceid><addsrcrecordid>eNqFkT1PwzAQhi0EEqUw8A8iscCQ1l-xnbFU5UMgGIDZMs6ldeXEIU6Q-u9JaQcEA9PppOfeu_dehM4JnhDKxdT6CWGYUXqARoRxlWJJskM0wkyIVGJKj9FJjGuMscoZHaGHl03drSC6mJi6SK5d8GHprPHJ4tP43nQu1Ekok1lsoF06710ByWz6BKEB34Xvdr5yFbQmnqKj0vgIZ_s6Rm83i9f5Xfr4fHs_nz2mlivcpSrLIRcFUGtZwVWZKQmlKJixueGiHG4EoCUFZZkFyIl8zwpMWK6AK45zycbocqfbtOGjh9jpykUL3psaQh81kZwLKbFU_6Mi40IoRviAXvxC16Fv68GIJlwqLDLKt7uvdpRtQ4wtlLppXWXajSZYbxPQ1utdAgMr9uwKqu1PY7AOus3aNKb-of5n8Av20ooD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1478065247</pqid></control><display><type>article</type><title>Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras</title><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Fuwa, Haruhiko ; Noto, Kenkichi ; Kawakami, Masato ; Sasaki, Makoto</creator><creatorcontrib>Fuwa, Haruhiko ; Noto, Kenkichi ; Kawakami, Masato ; Sasaki, Makoto</creatorcontrib><description>In this study, stereoisomeric aspergillide A/neopeltolide chimeras were synthesized in a parallel manner, and their antiproliferative activity was evaluated to demonstrate the potential utility of the 14-membered macrolactone structure embedded with a tetrahydropyran substructure as a template for developing natural product-like antiproliferative agents.</description><identifier>ISSN: 0366-7022</identifier><identifier>EISSN: 1348-0715</identifier><identifier>DOI: 10.1246/cl.130322</identifier><language>eng</language><publisher>Tokyo: The Chemical Society of Japan</publisher><subject>Antiproliferatives ; Biological ; Embedded structures ; Substructures ; Synthesis ; Utilities</subject><ispartof>Chemistry letters, 2013, Vol.42 (9), p.1020-1022</ispartof><rights>The Chemical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-859e96de2cc3d48f587ef6d3ac9a46f022ee2f2e8c3cee917b5d01398e4840973</citedby><cites>FETCH-LOGICAL-c480t-859e96de2cc3d48f587ef6d3ac9a46f022ee2f2e8c3cee917b5d01398e4840973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,4012,27910,27911,27912</link.rule.ids></links><search><creatorcontrib>Fuwa, Haruhiko</creatorcontrib><creatorcontrib>Noto, Kenkichi</creatorcontrib><creatorcontrib>Kawakami, Masato</creatorcontrib><creatorcontrib>Sasaki, Makoto</creatorcontrib><title>Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras</title><title>Chemistry letters</title><addtitle>Chemistry Letters</addtitle><description>In this study, stereoisomeric aspergillide A/neopeltolide chimeras were synthesized in a parallel manner, and their antiproliferative activity was evaluated to demonstrate the potential utility of the 14-membered macrolactone structure embedded with a tetrahydropyran substructure as a template for developing natural product-like antiproliferative agents.</description><subject>Antiproliferatives</subject><subject>Biological</subject><subject>Embedded structures</subject><subject>Substructures</subject><subject>Synthesis</subject><subject>Utilities</subject><issn>0366-7022</issn><issn>1348-0715</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkT1PwzAQhi0EEqUw8A8iscCQ1l-xnbFU5UMgGIDZMs6ldeXEIU6Q-u9JaQcEA9PppOfeu_dehM4JnhDKxdT6CWGYUXqARoRxlWJJskM0wkyIVGJKj9FJjGuMscoZHaGHl03drSC6mJi6SK5d8GHprPHJ4tP43nQu1Ekok1lsoF06710ByWz6BKEB34Xvdr5yFbQmnqKj0vgIZ_s6Rm83i9f5Xfr4fHs_nz2mlivcpSrLIRcFUGtZwVWZKQmlKJixueGiHG4EoCUFZZkFyIl8zwpMWK6AK45zycbocqfbtOGjh9jpykUL3psaQh81kZwLKbFU_6Mi40IoRviAXvxC16Fv68GIJlwqLDLKt7uvdpRtQ4wtlLppXWXajSZYbxPQ1utdAgMr9uwKqu1PY7AOus3aNKb-of5n8Av20ooD</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Fuwa, Haruhiko</creator><creator>Noto, Kenkichi</creator><creator>Kawakami, Masato</creator><creator>Sasaki, Makoto</creator><general>The Chemical Society of Japan</general><general>Chemical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>M7N</scope></search><sort><creationdate>2013</creationdate><title>Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras</title><author>Fuwa, Haruhiko ; Noto, Kenkichi ; Kawakami, Masato ; Sasaki, Makoto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-859e96de2cc3d48f587ef6d3ac9a46f022ee2f2e8c3cee917b5d01398e4840973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antiproliferatives</topic><topic>Biological</topic><topic>Embedded structures</topic><topic>Substructures</topic><topic>Synthesis</topic><topic>Utilities</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fuwa, Haruhiko</creatorcontrib><creatorcontrib>Noto, Kenkichi</creatorcontrib><creatorcontrib>Kawakami, Masato</creatorcontrib><creatorcontrib>Sasaki, Makoto</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuwa, Haruhiko</au><au>Noto, Kenkichi</au><au>Kawakami, Masato</au><au>Sasaki, Makoto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras</atitle><jtitle>Chemistry letters</jtitle><addtitle>Chemistry Letters</addtitle><date>2013</date><risdate>2013</risdate><volume>42</volume><issue>9</issue><spage>1020</spage><epage>1022</epage><pages>1020-1022</pages><issn>0366-7022</issn><eissn>1348-0715</eissn><abstract>In this study, stereoisomeric aspergillide A/neopeltolide chimeras were synthesized in a parallel manner, and their antiproliferative activity was evaluated to demonstrate the potential utility of the 14-membered macrolactone structure embedded with a tetrahydropyran substructure as a template for developing natural product-like antiproliferative agents.</abstract><cop>Tokyo</cop><pub>The Chemical Society of Japan</pub><doi>10.1246/cl.130322</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0366-7022
ispartof Chemistry letters, 2013, Vol.42 (9), p.1020-1022
issn 0366-7022
1348-0715
language eng
recordid cdi_proquest_miscellaneous_1744677078
source Oxford University Press Journals All Titles (1996-Current)
subjects Antiproliferatives
Biological
Embedded structures
Substructures
Synthesis
Utilities
title Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T19%3A40%3A56IST&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%20Biological%20Evaluation%20of%20Aspergillide%20A/Neopeltolide%20Chimeras&rft.jtitle=Chemistry%20letters&rft.au=Fuwa,%20Haruhiko&rft.date=2013&rft.volume=42&rft.issue=9&rft.spage=1020&rft.epage=1022&rft.pages=1020-1022&rft.issn=0366-7022&rft.eissn=1348-0715&rft_id=info:doi/10.1246/cl.130322&rft_dat=%3Cproquest_cross%3E1744677078%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=1478065247&rft_id=info:pmid/&rfr_iscdi=true