Synthesis of Galactocluster-Fluorquinolone Chimera Antibiotic
dc.contributor.advisor | Csávás, Magdolna | |
dc.contributor.advisordept | Debreceni Egyetem::Gyógyszerésztudományi Kar | hu_HU |
dc.contributor.author | Tran, Tu | |
dc.contributor.department | DE--Gyógyszerésztudományi Kar | hu_HU |
dc.contributor.opponent | Zita Tunde Tothne, Illyes | |
dc.contributor.opponent | Tósaki, Árpád | |
dc.contributor.opponentdept | Debreceni Egyetem::Gyógyszerésztudományi Kar | hu_HU |
dc.date.accessioned | 2021-05-03T12:45:04Z | |
dc.date.available | 2021-05-03T12:45:04Z | |
dc.date.created | 2021-03-02 | |
dc.description.abstract | The continual lung infection caused by Pseudomonas aeruginosa in most cystic fibrosis cases is nowadays a major concern. Multiresistance has made the production of new antibiotics an urgent necessity. A new synthetic idea of the possible antibiotic structure in which ciprofloxacin is attached to a trivalentgalactose cluster has been generated by our understanding of the relationship between bacterial lectin PA-IL and D-galactose. The method is to use a series of cupper-mediated azide- alkyne “click” reaction to join together propargylatedtetraethyelene bridges, scaffold, sugar (D- galactose) and finally, the antibiotics itself. | hu_HU |
dc.description.course | gyógyszerész | hu_HU |
dc.description.courselang | angol | hu_HU |
dc.description.coursespec | Biokémia-genomika | hu_HU |
dc.description.degree | MSc/MA | hu_HU |
dc.format.extent | 30 | hu_HU |
dc.identifier.uri | http://hdl.handle.net/2437/308186 | |
dc.language.iso | en | hu_HU |
dc.subject | Chimera Antibiotic | hu_HU |
dc.subject.dspace | DEENK Témalista::Kémia | hu_HU |
dc.title | Synthesis of Galactocluster-Fluorquinolone Chimera Antibiotic | hu_HU |
dc.title.subtitle | Synthesis of Galactocluster-Fluorquinolone Chimera Antibiotic | hu_HU |