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Kuder, Kamil
2011
Praca doktorska
The aim of this work was to obtain novel, active histamine H3 and H4 receptor ligands.Compounds were obtained according the proposed schemes based on lead structures, 47 in total. All of the obtained histamine H3 receptor ligands fit to the general histamine H3 receptor core proposed by Lipp. This group of compounds could be divided in two subgroups: piperazine and piperidine derivatives. Also, highly active fluorescent histamine H3 receptor ligand was obtained, as well as (cyclic)thiourea derivatives with expected histamine H4 receptor activity.Compounds were obtained via traditional organic synthesis, as well as with the use of microwave irradiation. All of the obtained derivatives were then tested in vitro for desired histamine receptor activity. For the group of piperidine derivatives lipophilicity studies were provided, using reversed phase planar chromatography method. Experimental values were then compared with values obtained by various computational programs. Fluorescent properties of one of the compounds were also studied.Computational approaches, allowed the in silico visualization of binding to histamine H3 receptor model described by Levoin et al
Kraków
2 - studia doktoranckie
chemia ; farmacja
Wydział Farmaceutyczny
Kieć-Kononowicz, Katarzyna
oai:dl.cm-uj.krakow.pl:3432
ZB-116237
pol; eng
tylko w bibliotece
Mar 17, 2023
Mar 6, 2013
42
0
http://dl.cm-uj.krakow.pl:8080/publication/3432
RDF
OAI-PMH
Więcek, Małgorzata
Szczepańska, Katarzyna
Łażewska, Dorota
Karcz, Tadeusz
Grosicki, Marek
Szafarz, Małgorzata
Mogilski, Szczepan
Citation style: chicago-author-date iso690-author-date
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