Experiments for the synthesis of carbohydrate-heterocycles hybrid molecule with potential galectin inhibitor activity

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dc.contributor.advisorJuhász, László
dc.contributor.authorBagaskara, Reyhan Kemal
dc.contributor.departmentDE--Természettudományi és Technológiai Kar--Kémiai Intézet
dc.date.accessioned2026-01-08T13:49:50Z
dc.date.available2026-01-08T13:49:50Z
dc.date.created2025-11-25
dc.description.abstractThe aim of this research was to develop a method for synthesizing 1,2-thiodisaccharide-type galectin inhibitors with a C-galactopyranosyl-heterocyclic unit. To achieve this, a cyanogalactal was used as a key intermediate which was synthesized from D-galactose in a three-step reaction. The cyanogalactal underwent an elimination reaction to obtain the galactal derivative. The derivative was then reacted with different thiols to give the desired galactal–benzothiazole hybrid.
dc.description.courseBiochemical Engineering
dc.description.degreeBSc/BA
dc.format.extent29
dc.identifier.urihttps://hdl.handle.net/2437/401828
dc.language.isoen
dc.rights.infoHozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében.
dc.subjectGalectin inhibitor
dc.subjectCarbohydrate-heterocycle hybrid
dc.subjectThiol-ene addition
dc.subject.dspaceChemistry::Organic Chemisty
dc.titleExperiments for the synthesis of carbohydrate-heterocycles hybrid molecule with potential galectin inhibitor activity
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