Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101528
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dc.contributorMainland Development Officeen_US
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorLv, Qen_US
dc.creatorLin, Yen_US
dc.creatorTan, Zen_US
dc.creatorJiang, Ben_US
dc.creatorXu, Len_US
dc.creatorRen, Hen_US
dc.creatorTai, WCSen_US
dc.creatorChan, COen_US
dc.creatorLee, CSen_US
dc.creatorGu, Zen_US
dc.creatorMok, DKWen_US
dc.creatorChen, Sen_US
dc.date.accessioned2023-09-18T07:30:44Z-
dc.date.available2023-09-18T07:30:44Z-
dc.identifier.issn2042-6496en_US
dc.identifier.urihttp://hdl.handle.net/10397/101528-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2019en_US
dc.rightsThe following publication Lv, Q., Lin, Y., Tan, Z., Jiang, B., Xu, L., Ren, H., ... & Chen, S. (2019). Dihydrochalcone-derived polyphenols from tea crab apple (Malus hupehensis) and their inhibitory effects on α-glucosidase in vitro. Food & function, 10(5), 2881-2887 is available at https://doi.org/10.1039/c9fo00229d.en_US
dc.titleDihydrochalcone-derived polyphenols from tea crab apple (Malus hupehensis) and their inhibitory effects on α-glucosidase in vitroen_US
dc.typeJournal/Magazine Articleen_US
dc.description.otherinformationTitle on author’s file: Dihydrochalcone-derived polyphenols from the crabapple tea (Malus hupehensis) and their inhibitory effects on α-glucosidase in vitroen_US
dc.identifier.spage2881en_US
dc.identifier.epage2887en_US
dc.identifier.volume10en_US
dc.identifier.issue5en_US
dc.identifier.doi10.1039/c9fo00229den_US
dcterms.abstractThree dihydrochalcone-derived polyphenols, huperolides A-C (1-3), along with thirteen known compounds (4-16) were isolated from the leaves of Malus hupehensis, the well-known tea crab apple in China. Their chemical structures were elucidated by extensive spectroscopic analysis including NMR (HSQC, HMBC, 1H-1H COSY and ROESY), HRMS and CD spectra. Huperolide A is a polyphenol with a new type of carbon skeleton, while huperolides B and C are a couple of atropisomers, which were isolated from natural sources for the first time. The antihyperglycemic effects of the isolated compounds were evaluated based on assaying their inhibitory activities against α-glucosidase. As a result, phlorizin (4), 3-hydroxyphloridzin (5), 3-O-coumaroylquinic acid (12) and β-hydroxypropiovanillone (15) showed significant concentration-dependent inhibitory effects on α-glucosidase. Therefore, those compounds might be responsible for the antihyperglycemic effect of this herb, and are the most promising compounds to lead discovery of drugs against diabetes.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationFood and function, 1 May 2019, v. 10, no. 5, p. 2881-2887en_US
dcterms.isPartOfFood and functionen_US
dcterms.issued2019-05-01-
dc.identifier.scopus2-s2.0-85066117309-
dc.identifier.pmid31070208-
dc.identifier.eissn2042-650Xen_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0398-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextBasic Research Foundation of Shenzhen Science and Technology Innovation Committee; National Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS22433668-
dc.description.oaCategoryGreen (AAM)en_US
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