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Syntheses of prodelphinidin B1, B2, and B4 and their antitumor activities against human PC-3 prostate cancer cell lines
http://hdl.handle.net/10091/17851
http://hdl.handle.net/10091/1785168f76a05-5920-47b7-8883-6a64d451e1b6
名前 / ファイル | ライセンス | アクション |
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Syntheses_prodelphinidin_B1_B2_B4_their_antitumor_activities.pdf (1.0 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2014-09-05 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Syntheses of prodelphinidin B1, B2, and B4 and their antitumor activities against human PC-3 prostate cancer cell lines | |||||
言語 | ||||||
言語 | eng | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.1016/j.tetlet.2013.10.113 | |||||
関連名称 | 10.1016/j.tetlet.2013.10.113 | |||||
キーワード | ||||||
主題 | Polyphenols, Synthesis, Natural product, Anticancer agents | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Fujii, Wataru
× Fujii, Wataru× Toda, Kazuya× Matsumoto, Kiriko× Kawaguchi, Koichiro× Kawahara, Sei-ichi× Hattori, Yasunao× Fujii, Hiroshi× Makabe, Hidefumi |
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信州大学研究者総覧へのリンク | ||||||
氏名 | Fujii, Hiroshi | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.WhymjeSh.html | |||||
信州大学研究者総覧へのリンク | ||||||
氏名 | Makabe, Hidefumi | |||||
URL | http://soar-rd.shinshu-u.ac.jp/profile/ja.jFSaPUkh.html | |||||
出版者 | ||||||
出版者 | PERGAMON-ELSEVIER SCIENCE LTD | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | TETRAHEDRON LETTERS. 54(52):7188-7192 (2013) | |||||
書誌情報 |
TETRAHEDRON LETTERS 巻 54, 号 52, p. 7188-7192, 発行日 2013-12-25 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Total synthesis of prodelphinidin B1, B2, and B4 has been accomplished. The key step is Lewis acid-mediated equimolar condensations between an epigallocatechin and/or a gallocatechin nucleophile and an epigallocatechin and/or a gallocatechin electrophile. The antitumor effects of synthetic prodelphinidin B1-B4 against human PC-3 prostate cancer cell lines have been investigated. These compounds showed significant antitumor effects. Their activity seemed to be little bit stronger than EGCG and prodelphinidin B3, known antitumor agent. | |||||
資源タイプ(コンテンツの種類) | ||||||
内容記述タイプ | Other | |||||
内容記述 | Article | |||||
ISSN | ||||||
収録物識別子タイプ | PISSN | |||||
収録物識別子 | 0040-4039 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00861801 | |||||
権利 | ||||||
権利情報 | Copyright© 2013 Elsevier Ltd. | |||||
出版タイプ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
WoS | ||||||
表示名 | Web of Science | |||||
URL | http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=ShinshuUniv&SrcApp=ShinshuUniv&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000327805800025 |