Please use this identifier to cite or link to this item: https://cuir.car.chula.ac.th/handle/123456789/80631
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dc.contributor.advisorWarinthorn Chavasiri-
dc.contributor.authorThamolwan Arnanthigo-
dc.contributor.authorNapassakorn Chuaycharoen-
dc.contributor.otherChulalongkorn University. Faculty of Science-
dc.date.accessioned2022-10-10T06:47:50Z-
dc.date.available2022-10-10T06:47:50Z-
dc.date.issued2020-
dc.identifier.urihttp://cuir.car.chula.ac.th/handle/123456789/80631-
dc.descriptionIn Partial Fulfillment for the Degree of Bachelor of Science Department of Chemistry, Faculty of Science Chulalongkorn University Academic Year 2020en_US
dc.description.abstractSynthesized depsides were modified based on the core structure of jaboticabin, to enhance its biological activities. Desired depsides were synthesized through an esterification with methyl 2-(2- hydroxyphenyl) acetate (NT0) and a carboxylic acid compound. DCC and DMAP were required to activate the carboxylic group and solvent used was DCM. 2-(2-Methoxy-2-oxoethyl)phenyl 3- nitrobenzoate (NT1) and 2-(2-methoxy-2-oxoethyl)phenyl (E)-3-(2,6-dichlorophenyl)acrylate (NT18) showed powerful anti ɑ-glucosidase activity with an IC50 value of 68.7 μM and 84.8 μM. The IC50 values obtained from assay were lower than that of Acarbose, the standard reference (IC50 = 93.6 μM). On the other hand, none of the compounds showed good potential towards antioxidant activities.en_US
dc.language.isoenen_US
dc.publisherChulalongkorn Universityen_US
dc.rightsChulalongkorn Universityen_US
dc.subjectDepsides -- Synthesisen_US
dc.subjectAntioxidants -- Synthesis -- Inhibitorsen_US
dc.titleSynthesis of depsides and their biological activityen_US
dc.typeSenior Projecten_US
dc.degree.grantorChulalongkorn Universityen_US
Appears in Collections:Sci - Senior Projects

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