Loading…

Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue

Glaziovianin A and its O7-propargyl analogue are potent cytotoxic isoflavones. We found that the O7-propargyl analogue completely arrested cell-cycle progression. We have achieved the large-scale synthesis of glaziovianin A and its O7-propargyl analogue for further in vivo experimentation.

Saved in:
Bibliographic Details
Published in:Bulletin of the Chemical Society of Japan 2014-04, Vol.87 (4), p.544-549
Main Authors: Hayakawa, Ichiro, Shioda, Shuya, Ikedo, Akiyuki, Kigoshi, Hideo
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333
cites cdi_FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333
container_end_page 549
container_issue 4
container_start_page 544
container_title Bulletin of the Chemical Society of Japan
container_volume 87
creator Hayakawa, Ichiro
Shioda, Shuya
Ikedo, Akiyuki
Kigoshi, Hideo
description Glaziovianin A and its O7-propargyl analogue are potent cytotoxic isoflavones. We found that the O7-propargyl analogue completely arrested cell-cycle progression. We have achieved the large-scale synthesis of glaziovianin A and its O7-propargyl analogue for further in vivo experimentation.
doi_str_mv 10.1246/bcsj.20130342
format article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1246_bcsj_20130342</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1246_bcsj_20130342</sourcerecordid><originalsourceid>FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333</originalsourceid><addsrcrecordid>eNo1kEFLwzAYhoMoOKdH7_kBZib50qY9jqFzMNhAPUr5kqYzozYjqcP66-1QT-_7Pof38BByK_hMSJXfG5v2M8kFcFDyjEwEqILxHNQ5mXDOSyZzDZfkKqX9OItMlRPyto1oe2-xpc9D17-75BMNDV22-O3D0WPnOzq_o0gXQx_68OUtXaXQtHgMnRt5V9NVn-iGaraN4YBxN7R03mEbdp_umlw02CZ385dT8vr48LJ4YuvNcrWYr5kVue6Za7jktc20yRFBqVI7UFgUulCguHA2s9JpkUuT8cbUti5HBsaBGZsBgClhv782hpSia6pD9B8Yh0rw6uSmOrmp_t3ADzOVV_o</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue</title><source>Oxford Journals Online</source><creator>Hayakawa, Ichiro ; Shioda, Shuya ; Ikedo, Akiyuki ; Kigoshi, Hideo</creator><creatorcontrib>Hayakawa, Ichiro ; Shioda, Shuya ; Ikedo, Akiyuki ; Kigoshi, Hideo</creatorcontrib><description>Glaziovianin A and its O7-propargyl analogue are potent cytotoxic isoflavones. We found that the O7-propargyl analogue completely arrested cell-cycle progression. We have achieved the large-scale synthesis of glaziovianin A and its O7-propargyl analogue for further in vivo experimentation.</description><identifier>ISSN: 0009-2673</identifier><identifier>EISSN: 1348-0634</identifier><identifier>DOI: 10.1246/bcsj.20130342</identifier><language>eng</language><ispartof>Bulletin of the Chemical Society of Japan, 2014-04, Vol.87 (4), p.544-549</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333</citedby><cites>FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Hayakawa, Ichiro</creatorcontrib><creatorcontrib>Shioda, Shuya</creatorcontrib><creatorcontrib>Ikedo, Akiyuki</creatorcontrib><creatorcontrib>Kigoshi, Hideo</creatorcontrib><title>Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue</title><title>Bulletin of the Chemical Society of Japan</title><description>Glaziovianin A and its O7-propargyl analogue are potent cytotoxic isoflavones. We found that the O7-propargyl analogue completely arrested cell-cycle progression. We have achieved the large-scale synthesis of glaziovianin A and its O7-propargyl analogue for further in vivo experimentation.</description><issn>0009-2673</issn><issn>1348-0634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo1kEFLwzAYhoMoOKdH7_kBZib50qY9jqFzMNhAPUr5kqYzozYjqcP66-1QT-_7Pof38BByK_hMSJXfG5v2M8kFcFDyjEwEqILxHNQ5mXDOSyZzDZfkKqX9OItMlRPyto1oe2-xpc9D17-75BMNDV22-O3D0WPnOzq_o0gXQx_68OUtXaXQtHgMnRt5V9NVn-iGaraN4YBxN7R03mEbdp_umlw02CZ385dT8vr48LJ4YuvNcrWYr5kVue6Za7jktc20yRFBqVI7UFgUulCguHA2s9JpkUuT8cbUti5HBsaBGZsBgClhv782hpSia6pD9B8Yh0rw6uSmOrmp_t3ADzOVV_o</recordid><startdate>20140415</startdate><enddate>20140415</enddate><creator>Hayakawa, Ichiro</creator><creator>Shioda, Shuya</creator><creator>Ikedo, Akiyuki</creator><creator>Kigoshi, Hideo</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140415</creationdate><title>Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue</title><author>Hayakawa, Ichiro ; Shioda, Shuya ; Ikedo, Akiyuki ; Kigoshi, Hideo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayakawa, Ichiro</creatorcontrib><creatorcontrib>Shioda, Shuya</creatorcontrib><creatorcontrib>Ikedo, Akiyuki</creatorcontrib><creatorcontrib>Kigoshi, Hideo</creatorcontrib><collection>CrossRef</collection><jtitle>Bulletin of the Chemical Society of Japan</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hayakawa, Ichiro</au><au>Shioda, Shuya</au><au>Ikedo, Akiyuki</au><au>Kigoshi, Hideo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue</atitle><jtitle>Bulletin of the Chemical Society of Japan</jtitle><date>2014-04-15</date><risdate>2014</risdate><volume>87</volume><issue>4</issue><spage>544</spage><epage>549</epage><pages>544-549</pages><issn>0009-2673</issn><eissn>1348-0634</eissn><abstract>Glaziovianin A and its O7-propargyl analogue are potent cytotoxic isoflavones. We found that the O7-propargyl analogue completely arrested cell-cycle progression. We have achieved the large-scale synthesis of glaziovianin A and its O7-propargyl analogue for further in vivo experimentation.</abstract><doi>10.1246/bcsj.20130342</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0009-2673
ispartof Bulletin of the Chemical Society of Japan, 2014-04, Vol.87 (4), p.544-549
issn 0009-2673
1348-0634
language eng
recordid cdi_crossref_primary_10_1246_bcsj_20130342
source Oxford Journals Online
title Practical Synthesis of Glaziovianin A, a Cytotoxic Isoflavone, and Its O 7-Propargyl Analogue
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T12%3A49%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Practical%20Synthesis%20of%20Glaziovianin%20A,%20a%20Cytotoxic%20Isoflavone,%20and%20Its%20O%207-Propargyl%20Analogue&rft.jtitle=Bulletin%20of%20the%20Chemical%20Society%20of%20Japan&rft.au=Hayakawa,%20Ichiro&rft.date=2014-04-15&rft.volume=87&rft.issue=4&rft.spage=544&rft.epage=549&rft.pages=544-549&rft.issn=0009-2673&rft.eissn=1348-0634&rft_id=info:doi/10.1246/bcsj.20130342&rft_dat=%3Ccrossref%3E10_1246_bcsj_20130342%3C/crossref%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c167t-ef020dc57b6aa34497e34a887843401ec5c2e7162b50fbdcd91ec3be3bd91b333%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true