Please use this identifier to cite or link to this item: http://nuir.lib.nu.ac.th/dspace/handle/123456789/6229
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dc.contributorMeranee Kidruangphokinen
dc.contributorเมราณีย์ กิตติ์เรืองโภคินth
dc.contributor.advisorSurat Boonphongen
dc.contributor.advisorสุรัตน์ บุญผ่องth
dc.contributor.otherNaresuan Universityen
dc.date.accessioned2024-08-27T06:17:13Z-
dc.date.available2024-08-27T06:17:13Z-
dc.date.created2022en_US
dc.date.issued26/10/2022en_US
dc.identifier.urihttp://nuir.lib.nu.ac.th/dspace/handle/123456789/6229-
dc.description.abstractThis study described the phytochemical studies, α-glucosidase inhibitory activity, and antioxidants of Alpinia mutica and Lysiphyllum strychnifolium, along with the optimal infusion conditions for L. strychnifolium leaves tea. The study is divided into three sections listed below. First, the chemical constituents and a-glucosidase inhibitory activity of A. mutica were investigated. The dichloromethane crude extracts of pericarps and seeds were analyzed by GC-MS in this section. The main volatile constituent of the pericarp extract was diarylheptanoid, namely 1,7-diphenyl-4,6-heptadien-3-one (45.28%). The most abundant volatile components in the seed extract were 5,6-dehydrokawain (64.94%), pinocembrin (22.51%) and farnesol (9.18%). Moreover, seven known compounds, including farnesol (1), 5,6-dehydrokawain (2), pinocembrin (3), cardamomin (4), naringenin (5), pinocembrin chalcone (6), and alpinetin (7) were isolated from dichloromethane extract of A. mutica seed and evaluated for α-glucosidase inhibitory activity. The most potent isolated compound against α-glucosidase was naringenin (5) with an IC50 value of 8.77 ± 1.04 μM. The chemical constituents, a-glucosidase inhibitory and antioxidant activities of L. strychnifolium were subsequently investigated. In this section, thirteen compounds, including astilbin (8), isoastilbin (9), neoastilbin (10), epicatechin (11), (E)-resveratrol (12), (E)-resveratrol 4'-O-β-D-glucoside (13), quercetin 3-O-β-D-arabinoside (14), phloretin (15), phloretin 4'-O-β-D-glucoside (16), phloretin 4'-O-(6''-O-galloyl)-β-D-glucoside (17), pinitol (18), gallic acid (19) and gallic acid ethyl ester (20) were isolated from the crude ethanolic extract of L. strychnifolium roots, stems, leaves and flowers. Compound 17 exhibited strong α-glucosidase inhibitory activity with an IC50 value of 16.2 ± 1.4 μM. In addition, compound 17 exhibited the highest antioxidant activity with an IC50 value of 19.26 ± 0.95 μM. The results of these two sections demonstrated that compounds 5 and 17 may provide therapeutic alternatives for type 2 diabetes. The final part of the research focused on determining the optimal infusion conditions for L. strychnifolium leaves tea. In this section, the effects of infusion conditions, including time, temperature and water volume, as well as multiple infusions, were investigated. L. strychnifolium leaves tea had the highest extraction yield (26.99 ± 0.33%) when brewed using hot water at 70 °C with a leaf powder and water ratio of 1:40 (g/mL) for 5 min, followed by two steps of brewing. Moreover, a sweetener, phloretin 4'-O-β-D-glucoside (16) and anti-hyperglycemia agent, pinitol (18), were identified as the major components of L. strychnifolium leaves tea. This section provides evidence for the folk belief that L. strychnifolium tea promotes health and wellness.en
dc.description.abstract      th
dc.language.isoenen_US
dc.publisherNaresuan Universityen_US
dc.rightsNaresuan Universityen_US
dc.subjectAlpiniaen
dc.subjectAlpinia muticaen
dc.subjectLysiphyllumen
dc.subjectLysiphyllum strychnifoliumen
dc.subjectBauhinia strchnifoliaen
dc.subjectα-Glucosidaseen
dc.subjectAntioxidanten
dc.subjectFlavonoiden
dc.subjectChemical constituentsen
dc.subjectVolatile componenten
dc.subjectbrewingen
dc.subject.classificationChemistryen
dc.subject.classificationProfessional, scientific and technical activitiesen
dc.subject.classificationChemistryen
dc.titleChemical constituents and biological activities of Alpinia mutica Roxb.  and Lysiphyllum strychnifolium (Craib) A. Schmitzen
dc.title-th
dc.typeThesisen
dc.typeวิทยานิพนธ์th
dc.contributor.coadvisorSurat Boonphongen
dc.contributor.coadvisorสุรัตน์ บุญผ่องth
dc.contributor.emailadvisorsuratb@nu.ac.then_US
dc.contributor.emailcoadvisorsuratb@nu.ac.then_US
dc.description.degreenameDoctor of Philosophy (Ph.D.)en
dc.description.degreenameปรัชญาดุษฎีบัณฑิต (ปร.ด.)th
dc.description.degreelevelDoctoral Degreeen
dc.description.degreelevelปริญญาเอกth
dc.description.degreedisciplineDepartment of Chemistryen
dc.description.degreedisciplineภาควิชาเคมีth
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