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Olejarz-Maciej, Agnieszka
2024
Praca doktorska
The multidirectional activity of ligands creates the possibility of more favourable treatment of diseases with a complicated pathomechanism. The functional selectivity showed by the G protein-coupled receptors ligands allows selective interaction with the desired signal transduction pathway resulting in a more favourable activity and safety profile of ligand. The first part of the work focused on determining the effect of H3 (H3R) and H4 (H4R) histamine receptor ligands on various intracellular signalling pathways. The intrinsic activity of H3R and H4R ligands was determined. Among the H4R ligands with a thiophene moiety, compounds showing functional selectivity were found. The second part of the work focused on the search for multi-target ligands with potential use in the treatment of neurodegenerative diseases. The following multi-target activities were considered: H3R affinity and monoamine oxidase B (MAO-B) inhibition or affinity for A1 and A2A adenosine receptors with MAO-B inhibition. The effect of compounds on MAO-B was examined. Good dual activity of H3R - MAO-B was confirmed. Active MAO-B inhibitors have been found in the group of adenosine receptors’ ligands. The obtained results provided important insight into the structure-activity relationship. They should also contribute to the development of new functionally selective and multi-target ligands.
Kraków
2 - studia doktoranckie
farmacja ; neurologia
Rada Dyscypliny Nauki farmaceutyczne
Kieć-Kononowicz, Katarzyna ; Karcz, Tadeusz
2023
oai:dl.cm-uj.krakow.pl:5140
ZB-139866
eng; pol
tylko w bibliotece
Dec 6, 2024
Jul 11, 2024
8
0
http://www.dl.cm-uj.krakow.pl:8080/publication/5141
RDF
OAI-PMH
Śniecikowska, Joanna
Głuch-Lutwin, Monika
Kuder, Kamil
Citation style: chicago-author-date iso690-author-date chicago-author-date
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