Advanced search ?

Object

Access Limited

This publication is protected and can be accessed only from certain IPs.
This publication is protected and can be accessed only from certain IPs.

Title: Synthesis and physicochemical studies of new aminalkyl derivatives of succinimide with potential anticonvulsant activity

Author:

Rybka, Sabina

Date:

2018

Type:

Praca doktorska

Abstract:

In the introduction of the doctoral thesis, different ways of searching for new anticonvulsants were described. New drugs obtained as a result of modifications of antiepileptic drugs and some examples of drugs with new structures which are different from the known antiepileptic drugs were also presented.The aim of the work was to obtain series of pyrrolidine-2,5-dione derivatives containing various moieties at position-3, and 4-substituted piperazine, piperidine or morpholine linked to imidazole atom by various length of alkylene chains, with potential anticonvulsant activity.In the experimental section, the synthesis of planned derivatives was described. As a result, 132 compounds were obtained. The structures of synthesized compounds were confirmed by elemental analysis and 1H-NMR, 13C-NMR, 19F-NMR and LC/MS spectra, whereas purity and homogeneity by chromatographic methods.Anticonvulsant activity was examined using MES, scPTZ and 6 Hz tests. Based on these results, the structure-activity relationship was determined. In addition, the probable mechanism of action was identified for the most active compounds, and it was associated with the blocking of sodium channels and/or calcium L-channels.Moreover, lipophilicity was determined for selected derivatives, and the lipophilicity-activity relationship was established, as well. Metabolism of selected compounds was also tested.

Place of publishing:

Kraków

Level of degree:

2 - studia doktoranckie

Degree discipline:

farmacja

Degree grantor:

Wydział Farmaceutyczny

Promoter:

Obniska, Jolanta

Date issued:

2017

Identifier:

oai:dl.cm-uj.krakow.pl:4389

Call number:

ZB-128500

Language:

pol; eng

Access rights:

tylko w bibliotece

Subject and keywords:

anticonvulsant activity succinimide pyrrolidine-2 5-dione

Object collections:

Last modified:

Mar 14, 2023

In our library since:

Oct 13, 2020

Number of object content hits:

8

Number of object content views in PDF format

0

All available object's versions:

http://dl.cm-uj.krakow.pl:8080/publication/4390

Show description in RDF format:

RDF

Show description in OAI-PMH format:

OAI-PMH

Edition name Date
ZB-128500 Mar 14, 2023

Objects

Similar

Synthesis and physicochemical studies of new aminalkyl derivatives of succinimide with potential anticonvulsant activity

Rybka, Sabina

2018
Praca doktorska

Synthesis and chemical-pharmacological studies of new derivatives 1,3-substituted pyrrolidine-2,5-dione with potential anticonvulsant activity

Góra, Małgorzata

2021
Praca doktorska

Chemical and pharmacological studies of N-phenylamino succinimides with potential anticonvulsant activity

Kamiński, Krzysztof

2008
Praca doktorska

Chemical and pharmacological studies in group of 3,3-disubstituted derivatives of pyrrolidyne-2,5-dion with potential anticonvulsant activity

Chlebek, Iwona

2013
Praca doktorska

Structure - anticonvulsant activity relationship in the group of aminoalkanol derivatives

Gunia-Krzyżak, Agnieszka

2013
Praca doktorska

Synthesis and pharmacological properties of novel derivatives of [gamma]-butyrolacotone and amides of [gamma]-hydroxybutyric acid

Więckowski, Krzysztof

2008
Praca doktorska

The mechanism of antiarrhythmic activity of the new pyrrolidin-2-one and methylazetidine derivatives

Lustyk, Klaudia

2019
Praca doktorska

Design and synthesis of modified amino acid derivatives with potential antiseizure and antinociceptice activity

Jakubiec, Marcin

2025
Praca doktorska
More
×

Citation

Citation style:

Contact details

Address

Medical Library
Medyczna 7
30-688 Krakow

Phone

12 658 72 56
517 385 669

E-Mail

Collecting and Elaboration Department
cyfrowabm@cm-uj.krakow.pl

Visit us!

This page uses 'cookies'. More information