{"created":"2024-01-16T06:08:05.336315+00:00","id":2000071,"links":{},"metadata":{"_buckets":{"deposit":"4c2b1567-10cd-47d7-b4b0-6f39b76277f4"},"_deposit":{"created_by":8,"id":"2000071","owner":"8","owners":[8],"pid":{"revision_id":0,"type":"depid","value":"2000071"},"status":"published"},"_oai":{"id":"oai:fra.repo.nii.ac.jp:02000071","sets":["15"]},"author_link":["453"],"control_number":"2000071","item_10001_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueNumber":"5","bibliographicNumberOfPages":"5","bibliographicPageEnd":"5","bibliographicPageStart":"1","bibliographicVolumeNumber":"18","bibliographic_titles":[{"bibliographic_title":"Natural Product Communications","bibliographic_titleLang":"en"}]}]},"item_10001_description_5":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"Some aplysiatoxin-related compounds have been isolated from an Okinawan cyanobacterium Okeania hirsuta. The structure of a natural product isolated as 30-methyloscillatoxin D(1a) from this cyanobacterium in our previous report was re-investigated and revised to be a 7-epimer of 30-methyloscillatoxin D(4a) using precise NMR analysis. The synthesis of O-Me-7-epi-30-methyloscillatoxin D(4b) led to confirmation of the stereochemistry of 4a. This is the first report of a 7-epi-typeaplysiatoxin-related compound from a natural source.","subitem_description_language":"en","subitem_description_type":"Abstract"}]},"item_10001_publisher_8":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"SAGE 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