{"created":"2020-03-08T23:44:36.296973+00:00","id":2622,"links":{},"metadata":{"_buckets":{"deposit":"0966e4ea-7820-4ef7-8e29-4e586d4dcda3"},"_deposit":{"id":"2622","owners":[],"pid":{"revision_id":0,"type":"recid","value":"2622"},"status":"published"},"_oai":{"id":"oai:meral.edu.mm:recid/2622","sets":["1582963390870:1582967633684"]},"communities":["ccm","ccp","kyauksetu","ltc","maas","miit","mlmu","mmu","mtlu","mtu","mub","mude","mufl","pathein","scu","suoe","tcu","tgu","tuh","tum","ucsm","ucsmtla","ucsmub","ucspathein","ucstaungoo","ucsy","udmm","udmy","uit","um","um1","um2","umkn","umm","uphy","urj","uvs","uy","yau","ydbu","ytu","yude","yueco","yufl","yuoe"],"control_number":"2622","item_1583103067471":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_1551255647225":"Niruriflavone, a new Antioxidant Flavone Sulfonic Acid from Phyllanthus niruri","subitem_1551255648112":"en"}]},"item_1583103085720":{"attribute_name":"Description","attribute_value_mlt":[{"interim":"A new flavone sulfonic acid 1 named niruriflavone was isolated from the 70% ethanolic extract of the whole plant of Phyllanthus niruri (Euphorbiaceae), together with 6,10,14-trimethyl-2- pentadecanone, hypophyllanthin, gallic acid, brevifolin carboxylic acid, methyl brevifolin carboxylate, isoquercetin, quercetin-3-O-ß-D-glucopyranosyl(1→4)-α-rhamnopyranoside, corilagin, and isocorilagin, whose structures were determined by spectroscopic methods and comparison with published data. In an ABTS cation radical reduction assay, niruriflavone (1) exhibited potent radical scavenging properties. A biological test system based on bioluminescence of the dinoflagellate Lingulodinium polyedrum did not reveal any prooxidant properties of 1 at 50 μM."}]},"item_1583103108160":{"attribute_name":"Keywords","attribute_value_mlt":[{"interim":"Phyllanthus niruri"}]},"item_1583103120197":{"attribute_name":"Files","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_access","date":[{"dateType":"Available","dateValue":"2020-05-05"}],"displaytype":"preview","filename":"166_Niruriflavone-Ni Ni Than.pdf","filesize":[{"value":"186 Kb"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"url":"https://meral.edu.mm/record/2622/files/166_Niruriflavone-Ni Ni Than.pdf"},"version_id":"2b544df2-2145-405f-bb3f-6ddd96b3ad3a"}]},"item_1583103131163":{"attribute_name":"Journal articles","attribute_value_mlt":[{"subitem_journal_title":"A Journal of Chemical Sciences","subitem_volume":"61"}]},"item_1583103147082":{"attribute_name":"Conference papaers","attribute_value_mlt":[{}]},"item_1583103211336":{"attribute_name":"Books/reports/chapters","attribute_value_mlt":[{}]},"item_1583103233624":{"attribute_name":"Thesis/dissertations","attribute_value_mlt":[{"subitem_supervisor(s)":[]}]},"item_1583105942107":{"attribute_name":"Authors","attribute_value_mlt":[{"subitem_authors":[{"subitem_authors_fullname":"Ni Ni Than"},{"subitem_authors_fullname":"Fotso, S."},{"subitem_authors_fullname":"Poeggeler, B."},{"subitem_authors_fullname":"Hardeland, R."},{"subitem_authors_fullname":"Laatsch, H."}]}]},"item_1583108359239":{"attribute_name":"Upload type","attribute_value_mlt":[{"interim":"Publication"}]},"item_1583108428133":{"attribute_name":"Publication type","attribute_value_mlt":[{"interim":"Journal article"}]},"item_1583159729339":{"attribute_name":"Publication date","attribute_value":"2006"},"item_1583159847033":{"attribute_name":"Identifier","attribute_value":"https://uyr.uy.edu.mm/handle/123456789/980"},"item_title":"Niruriflavone, a new Antioxidant Flavone Sulfonic Acid from Phyllanthus niruri","item_type_id":"21","owner":"1","path":["1582967633684"],"publish_date":"2020-03-05","publish_status":"0","recid":"2622","relation_version_is_last":true,"title":["Niruriflavone, a new Antioxidant Flavone Sulfonic Acid from Phyllanthus niruri"],"weko_creator_id":"1","weko_shared_id":-1},"updated":"2021-12-13T02:12:31.348806+00:00"}