α-Glucosidase Inhibitory Activity and Anti-Adipogenic Effect of Compounds from Dendrobium delacourii

dc.contributor.authorThant M.T.
dc.contributor.authorKhine H.E.E.
dc.contributor.authorNealiga J.Q.L.
dc.contributor.authorChatsumpun N.
dc.contributor.authorChaotham C.
dc.contributor.authorSritularak B.
dc.contributor.authorLikhitwitayawuid K.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T16:49:13Z
dc.date.available2023-06-18T16:49:13Z
dc.date.issued2022-02-01
dc.description.abstractChemical investigation of Dendrobium delacourii revealed 11 phenolic compounds, and the structures of these compounds were determined by analysis of their NMR and HR-ESI-MS data. All compounds were investigated for their α-glucosidase inhibitory activity and anti-adipogenic properties. Phoyunnanin E (10) and phoyunnanin C (11) showed the most potent α-glucosidase inhibition by comparing with acarbose, which was used as a positive control. Kinetic study revealed the non-competitive inhibitors against the enzyme. For anti-adipogenic activity, densifloral B (3) showed the strongest inhibition when compared with oxyresveratrol (positive control). In addition, densifloral B might be responsible for the inhibition of adipocyte differentiation via downregulating the expression of peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT enhancer-binding protein alpha (C/EBPα), which are major transcription factors in adipogenesis.
dc.identifier.citationMolecules Vol.27 No.4 (2022)
dc.identifier.doi10.3390/molecules27041156
dc.identifier.eissn14203049
dc.identifier.pmid35208957
dc.identifier.scopus2-s2.0-85124598010
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/83835
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleα-Glucosidase Inhibitory Activity and Anti-Adipogenic Effect of Compounds from Dendrobium delacourii
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124598010&origin=inward
oaire.citation.issue4
oaire.citation.titleMolecules
oaire.citation.volume27
oairecerif.author.affiliationChulalongkorn University
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationUniversity of Pharmacy

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