WEKO3
アイテム
{"_buckets": {"deposit": "4eddf263-3a00-42f0-a70a-886ccb43d0a0"}, "_deposit": {"id": "10252", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "10252"}, "status": "published"}, "_oai": {"id": "oai:soar-ir.repo.nii.ac.jp:00010252", "sets": ["1017"]}, "author_link": ["32386", "32387", "32388", "32389", "32390", "32391", "32392", "32393"], "item_1628147817048": {"attribute_name": "出版タイプ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_ab4af688f83e57aa", "subitem_version_type": "AM"}]}, "item_6_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2013-04-29", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "17", "bibliographicPageEnd": "3550", "bibliographicPageStart": "3543", "bibliographicVolumeNumber": "69", "bibliographic_titles": [{"bibliographic_title": "TETRAHEDRON"}]}]}, "item_6_description_20": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Total synthesis of prodelphinidin B3 and C2 have been accomplished. The key step is Lewis acid-mediated equimolar condensations between a catechin and/or gallocatechin nucleophile and a gallocatechin electrophile. The antitumor effects of synthetic prodelphidin B3 and C2 against PC-3 prostate cancer cell lines have been investigated. Both compounds showed significant antitumor effects. Their activity was almost the same as that of EGCG, a known antitumor agent.", "subitem_description_type": "Abstract"}]}, "item_6_description_30": {"attribute_name": "資源タイプ(コンテンツの種類)", "attribute_value_mlt": [{"subitem_description": "Article", "subitem_description_type": "Other"}]}, "item_6_description_5": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "TETRAHEDRON. 69(17):3543-3550 (2013)", "subitem_description_type": "Other"}]}, "item_6_link_3": {"attribute_name": "信州大学研究者総覧へのリンク", "attribute_value_mlt": [{"subitem_link_text": "Fujii, Hiroshi", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.WhymjeSh.html"}, {"subitem_link_text": "Makabe, Hidefumi", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.jFSaPUkh.html"}]}, "item_6_link_67": {"attribute_name": "WoS", "attribute_value_mlt": [{"subitem_link_text": "Web of Science", "subitem_link_url": "http://gateway.isiknowledge.com/gateway/Gateway.cgi?\u0026GWVersion=2\u0026SrcAuth=ShinshuUniv\u0026SrcApp=ShinshuUniv\u0026DestLinkType=FullRecord\u0026DestApp=WOS\u0026KeyUT=000316922700004"}]}, "item_6_publisher_4": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "PERGAMON-ELSEVIER SCIENCE LTD"}]}, "item_6_relation_48": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_name": [{"subitem_relation_name_text": "10.1016/j.tet.2013.02.087"}], "subitem_relation_type_id": {"subitem_relation_type_id_text": "https://doi.org/10.1016/j.tet.2013.02.087", "subitem_relation_type_select": "DOI"}}]}, "item_6_rights_62": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "Copyright© 2013 Elsevier Ltd."}]}, "item_6_select_64": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_6_source_id_35": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0040-4020", "subitem_source_identifier_type": "ISSN"}]}, "item_6_source_id_39": {"attribute_name": "NII ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0040-4020", "subitem_source_identifier_type": "ISSN"}]}, "item_6_source_id_40": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00861787", "subitem_source_identifier_type": "NCID"}]}, "item_6_text_69": {"attribute_name": "wosonly authkey", "attribute_value_mlt": [{"subitem_text_value": "Polyphenols; Synthesis; Natural product; Anticancer agents"}]}, "item_6_text_70": {"attribute_name": "wosonly keywords", "attribute_value_mlt": [{"subitem_text_value": "EFFICIENT STEREOSELECTIVE-SYNTHESIS; MEDIATED EQUIMOLAR CONDENSATION; POLYMERASE INHIBITORY-ACTIVITY; RADICAL SCAVENGING ACTIVITY; OCCURRING O-HETEROCYCLES; OLIGOMERIC PROANTHOCYANIDINS; POLYPHENOL CHEMISTRY; SYSTEMATIC SYNTHESIS; MAILLARD REACTION; INTERFLAVAN BOND"}]}, "item_6_textarea_68": {"attribute_name": "wosonly abstract", "attribute_value_mlt": [{"subitem_textarea_value": "Total synthesis of prodelphinidin B3 and C2 have been accomplished. The key step is Lewis acid-mediated equimolar condensations between a catechin and/or gallocatechin nucleophile and a gallocatechin electrophile. The antitumor effects of synthetic prodelphidin B3 and C2 against PC-3 prostate cancer cell lines have been investigated. Both compounds showed significant antitumor effects. Their activity was almost the same as that of EGCG, a known antitumor agent. © 2013 Elsevier Ltd. All rights reserved."}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Fujii, Wataru"}], "nameIdentifiers": [{"nameIdentifier": "32386", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Toda, Kazuya"}], "nameIdentifiers": [{"nameIdentifier": "32387", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kawaguchi, Koichiro"}], "nameIdentifiers": [{"nameIdentifier": "32388", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kawahara, Sei-ichi"}], "nameIdentifiers": [{"nameIdentifier": "32389", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Katoh, Miyuki"}], "nameIdentifiers": [{"nameIdentifier": "32390", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Hattori, Yasunao"}], "nameIdentifiers": [{"nameIdentifier": "32391", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Fujii, Hiroshi"}], "nameIdentifiers": [{"nameIdentifier": "32392", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Makabe, Hidefumi"}], "nameIdentifiers": [{"nameIdentifier": "32393", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2015-09-25"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "Syntheses_prodelphinidin_B3_C2_their_antitumor.pdf", "filesize": [{"value": "1.1 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_note", "mimetype": "application/pdf", "size": 1100000.0, "url": {"label": "Syntheses_prodelphinidin_B3_C2_their_antitumor.pdf", "url": "https://soar-ir.repo.nii.ac.jp/record/10252/files/Syntheses_prodelphinidin_B3_C2_their_antitumor.pdf"}, "version_id": "0aa24942-f5a6-4e51-af47-a072472eccfe"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "Polyphenols", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Synthesis", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Natural product", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Anticancer agents", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "journal article", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "Syntheses of prodelphinidin B3 and C2, and their antitumor activities through cell cycle arrest and caspase-3 activation", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Syntheses of prodelphinidin B3 and C2, and their antitumor activities through cell cycle arrest and caspase-3 activation", "subitem_title_language": "en"}]}, "item_type_id": "6", "owner": "1", "path": ["1017"], "permalink_uri": "http://hdl.handle.net/10091/17847", "pubdate": {"attribute_name": "PubDate", "attribute_value": "2014-09-05"}, "publish_date": "2014-09-05", "publish_status": "0", "recid": "10252", "relation": {}, "relation_version_is_last": true, "title": ["Syntheses of prodelphinidin B3 and C2, and their antitumor activities through cell cycle arrest and caspase-3 activation"], "weko_shared_id": -1}
Syntheses of prodelphinidin B3 and C2, and their antitumor activities through cell cycle arrest and caspase-3 activation
http://hdl.handle.net/10091/17847
http://hdl.handle.net/10091/1784728379036-0764-4457-97aa-8b02745a9c59
名前 / ファイル | ライセンス | アクション |
---|---|---|
![]() |
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2014-09-05 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Syntheses of prodelphinidin B3 and C2, and their antitumor activities through cell cycle arrest and caspase-3 activation | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Polyphenols | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Synthesis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Natural product | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | 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× Kawaguchi, Koichiro× Kawahara, Sei-ichi× Katoh, Miyuki× Hattori, Yasunao× Fujii, Hiroshi× Makabe, Hidefumi |
|||||
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. 69(17):3543-3550 (2013) | |||||
書誌情報 |
TETRAHEDRON 巻 69, 号 17, p. 3543-3550, 発行日 2013-04-29 |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Total synthesis of prodelphinidin B3 and C2 have been accomplished. The key step is Lewis acid-mediated equimolar condensations between a catechin and/or gallocatechin nucleophile and a gallocatechin electrophile. The antitumor effects of synthetic prodelphidin B3 and C2 against PC-3 prostate cancer cell lines have been investigated. Both compounds showed significant antitumor effects. Their activity was almost the same as that of EGCG, a 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 | ISSN | |||||
収録物識別子 | 0040-4020 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00861787 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.1016/j.tet.2013.02.087 | |||||
関連名称 | 10.1016/j.tet.2013.02.087 | |||||
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=000316922700004 |