Semisynthesis of C-ring modified triptolide analogues and their cytotoxic activities
The semisynthesis and SAR study of C-ring modified cytotoxic triptolide analogues were reported. Several C-ring modified analogues of a potent antileukemic diterpene, triptolide ( 1), were synthesized and their structure–activity relationships were studied.
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2006-04, Vol.16 (7), p.1947-1949 |
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container_end_page | 1949 |
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container_issue | 7 |
container_start_page | 1947 |
container_title | Bioorganic & medicinal chemistry letters |
container_volume | 16 |
creator | Aoyagi, Yutaka Hitotsuyanagi, Yukio Hasuda, Tomoyo Fukaya, Haruhiko Takeya, Koichi Aiyama, Ritsuo Matsuzaki, Takeshi Hashimoto, Shusuke |
description | The semisynthesis and SAR study of C-ring modified cytotoxic triptolide analogues were reported.
Several C-ring modified analogues of a potent antileukemic diterpene, triptolide (
1), were synthesized and their structure–activity relationships were studied. |
doi_str_mv | 10.1016/j.bmcl.2005.12.098 |
format | Article |
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Several C-ring modified analogues of a potent antileukemic diterpene, triptolide (
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Several C-ring modified analogues of a potent antileukemic diterpene, triptolide (
1), were synthesized and their structure–activity relationships were studied.</description><subject>Antineoplastic agents</subject><subject>Antitumor</subject><subject>Biological and medical sciences</subject><subject>C-ring</subject><subject>Cell Line, Tumor</subject><subject>Diterpenes - chemical synthesis</subject><subject>Diterpenes - chemistry</subject><subject>Diterpenes - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Epoxy Compounds</subject><subject>General aspects</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Models, Molecular</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenanthrenes - chemical synthesis</subject><subject>Phenanthrenes - chemistry</subject><subject>Phenanthrenes - pharmacology</subject><subject>Semisynthesis</subject><subject>Structure-Activity Relationship</subject><subject>Structure–activity relationships</subject><subject>Triptolide analogues</subject><issn>0960-894X</issn><issn>1464-3405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEuLFDEQgIMo7rj6BzxIX_TWbeXdAS8y-IIFD67gLaTT1bsZujtjklmcf2-GGdibXqoK6qui6iPkNYWOAlXvd92w-LljALKjrAPTPyEbKpRouQD5lGzAKGh7I35dkRc57wCoACGekyuqhJRMsA25_YFLyMe13GMOuYlTs21TWO-aJY5hCjg2JYV9iXMYsXGrm-PdAXOtauMeQ2r8scQS_wTfOF_CQygB80vybHJzxleXfE1-fv50u_3a3nz_8m378ab1gsrSDkIPetScaSEdlQPrQbiBT5xPgJ72RmpnNOsH9L3i3IGrceDGGcc1CMWvybvz3n2Kv-tZxdZfPM6zWzEeslVaGQAw_wWpBkW5lBVkZ9CnmHPCye5TWFw6Wgr2JN3u7Em6PUm3lNkqvQ69uWw_DAuOjyMXyxV4ewFc9m6eklt9yI-clopSyiv34cxhlfYQMNnsA64ex5DQFzvG8K87_gI2-p_F</recordid><startdate>20060401</startdate><enddate>20060401</enddate><creator>Aoyagi, Yutaka</creator><creator>Hitotsuyanagi, Yukio</creator><creator>Hasuda, Tomoyo</creator><creator>Fukaya, Haruhiko</creator><creator>Takeya, Koichi</creator><creator>Aiyama, Ritsuo</creator><creator>Matsuzaki, Takeshi</creator><creator>Hashimoto, Shusuke</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20060401</creationdate><title>Semisynthesis of C-ring modified triptolide analogues and their cytotoxic activities</title><author>Aoyagi, Yutaka ; Hitotsuyanagi, Yukio ; Hasuda, Tomoyo ; Fukaya, Haruhiko ; Takeya, Koichi ; Aiyama, Ritsuo ; Matsuzaki, Takeshi ; Hashimoto, Shusuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-b47b7d732745a15b2804ab3f33f0ec18957a9728bec8633a0a633b39a9a370463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Antineoplastic agents</topic><topic>Antitumor</topic><topic>Biological and medical sciences</topic><topic>C-ring</topic><topic>Cell Line, Tumor</topic><topic>Diterpenes - chemical synthesis</topic><topic>Diterpenes - chemistry</topic><topic>Diterpenes - pharmacology</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Epoxy Compounds</topic><topic>General aspects</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Models, Molecular</topic><topic>Pharmacology. 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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Antineoplastic agents Antitumor Biological and medical sciences C-ring Cell Line, Tumor Diterpenes - chemical synthesis Diterpenes - chemistry Diterpenes - pharmacology Drug Screening Assays, Antitumor Epoxy Compounds General aspects Humans Medical sciences Miscellaneous Models, Molecular Pharmacology. Drug treatments Phenanthrenes - chemical synthesis Phenanthrenes - chemistry Phenanthrenes - pharmacology Semisynthesis Structure-Activity Relationship Structure–activity relationships Triptolide analogues |
title | Semisynthesis of C-ring modified triptolide analogues and their cytotoxic activities |
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