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dc.contributor.advisorKļimenkovs, Igors
dc.contributor.authorŠadauskis, Jānis
dc.contributor.otherLatvijas Universitāte. Ķīmijas fakultāte
dc.date.accessioned2023-09-06T01:03:17Z
dc.date.available2023-09-06T01:03:17Z
dc.date.issued2023
dc.identifier.other96515
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/64193
dc.description.abstractBakalaura darba ietvaros tika sintezēti aizvietoti 1H-1,2,4-triazol-5-amīni, kā arī oksazolamīni un pirazolamīni, kas varētu būt potenciāli IRE1α inhibitori. Tika pētīta 1H-1,2,4-triazol-5-amīnu acilēšana un endocikliski acilēto savienojumu izomerizācija par eksocikliski acilētiem savienojumiem.
dc.description.abstractBachelor’s thesis is dedicated to the synthesis of substituted 1H-1,2,4-triazol-5-amines as well as substituted oxazolamines and pyrazolamines, that could be potential inhibitors of IRE1α. Acylation of 1H-1,2,4-triazol-5-amines and endocyclically acylated compound isomerization into exocyclically acylated compounds was investigated.
dc.language.isolav
dc.publisherLatvijas Universitāte
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectĶīmija
dc.subjectIRE1a
dc.subjectIRE1a INHIBITORI
dc.subject1,2,4-TRIAZOL-5-AMĪNU ACILĒŠANA
dc.subjectOKSAZOLAMĪNI
dc.subjectPIRAZOLAMĪNI
dc.titlePotenciālu IRE1a inhibitoru sintēze
dc.title.alternativeSynthesis of potencial IRE1a inhibitors
dc.typeinfo:eu-repo/semantics/bachelorThesis


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