{"created":"2023-05-15T16:30:26.640191+00:00","id":1572,"links":{},"metadata":{"_buckets":{"deposit":"7c8f37d3-191c-42c0-8568-df0b4f0e3338"},"_deposit":{"created_by":2,"id":"1572","owners":[2],"pid":{"revision_id":0,"type":"depid","value":"1572"},"status":"published"},"_oai":{"id":"oai:nagasaki-u.repo.nii.ac.jp:00001572","sets":["73:74"]},"author_link":["7563","7559","7565","7564","7560","7562","7561"],"item_2_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"1990-02-25","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"2","bibliographicPageEnd":"425","bibliographicPageStart":"422","bibliographicVolumeNumber":"38","bibliographic_titles":[{"bibliographic_title":"Chemical & Pharmaceutical Bulletin"}]}]},"item_2_description_4":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"Six more anisatin-like sesquiterpene lactones were isolated from the pericarps of Illicium majus. The structures of these sompounds (4-9) were characterized as majucins having a 2-oxy group. It is noteworthy that one of the six compounds has a (10S*)-hydroxyl group, whereas usual anisatin- and majucin-type compounds have a (10R*)-hydroxyl group. All these structures were determined on the basis of spectral data, compard with those of majucin and neomajucin. These compounds did not exhibit convulsive toxicity to mice, although the (10S*)-hydroxy compound was not examined.","subitem_description_type":"Abstract"}]},"item_2_description_63":{"attribute_name":"引用","attribute_value_mlt":[{"subitem_description":"Chemical & Pharmaceutical Bulletin, 38(2), pp.422-425; 1990","subitem_description_type":"Other"}]},"item_2_publisher_33":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"日本薬学会"}]},"item_2_relation_12":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type":"isIdenticalTo","subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1248/cpb.38.422","subitem_relation_type_select":"DOI"}}]},"item_2_rights_13":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"c The Pharmaceutical Society of Japan"}]},"item_2_source_id_10":{"attribute_name":"書誌レコードID","attribute_value_mlt":[{"subitem_source_identifier":"AA00602100","subitem_source_identifier_type":"NCID"}]},"item_2_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"00092363","subitem_source_identifier_type":"ISSN"}]},"item_2_source_id_8":{"attribute_name":"EISSN","attribute_value_mlt":[{"subitem_source_identifier":"13475223","subitem_source_identifier_type":"ISSN"}]},"item_2_text_62":{"attribute_name":"出版者別言語","attribute_value_mlt":[{"subitem_text_value":"Pharmaceutical Society of Japan"}]},"item_2_version_type_16":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"KOUNO, Isao"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"BABA, Naosuke"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"HASHIMOTO, Miwa"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"KAWANO, Nobusuke"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"TAKAHASHI, Masakatsu"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"KANETO, Hiroshi"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"YANG, Chun-Shu"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2020-12-18"}],"displaytype":"detail","filename":"CPB38_422.pdf","filesize":[{"value":"643.0 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"CPB38_422.pdf","url":"https://nagasaki-u.repo.nii.ac.jp/record/1572/files/CPB38_422.pdf"},"version_id":"5ca4f8aa-133d-45b0-99f5-0d1258629316"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"Illicium majus","subitem_subject_scheme":"Other"},{"subitem_subject":"Illiciaseae","subitem_subject_scheme":"Other"},{"subitem_subject":"sesquiterpene lactone","subitem_subject_scheme":"Other"},{"subitem_subject":"2-oxyneomajucin","subitem_subject_scheme":"Other"},{"subitem_subject":"2D COSY NMR","subitem_subject_scheme":"Other"},{"subitem_subject":"Chinese Illicium plant","subitem_subject_scheme":"Other"},{"subitem_subject":"3, 4-dehydroxyneomajucin","subitem_subject_scheme":"Other"},{"subitem_subject":"2-oxymajucin","subitem_subject_scheme":"Other"},{"subitem_subject":"majucin","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":"Sesquiterpene lactones from the pericarps of Illicium majus; 2-oxy derivatives of neomajucin and 3,4-dehydroxyneomajucin.","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Sesquiterpene lactones from the pericarps of Illicium majus; 2-oxy derivatives of neomajucin and 3,4-dehydroxyneomajucin."}]},"item_type_id":"2","owner":"2","path":["74"],"pubdate":{"attribute_name":"公開日","attribute_value":"2019-02-21"},"publish_date":"2019-02-21","publish_status":"0","recid":"1572","relation_version_is_last":true,"title":["Sesquiterpene lactones from the pericarps of Illicium majus; 2-oxy derivatives of neomajucin and 3,4-dehydroxyneomajucin."],"weko_creator_id":"2","weko_shared_id":-1},"updated":"2023-05-16T04:00:07.339131+00:00"}