Microwave synthesis of disubstituted pyrrolidine-2,5-dione derivatives

Succinimide (pyrrolidine-2,5-dione) derivatives are organic compounds with a broad spectrum of pharmacological activities. Analogs of this cyclic ureide are well-known and comercially available anticonvulsants (ethosuccinimide, metosuccinimide and fensuccinimide), antipsychotics, sedatives, anticanc...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Dimitrijević Marija
Gak Simić Kristina
Mašulović Aleksandra
Matović Luka
Lađarević Jelena
Banjac Nebojša
Trišović Nemanja
Lazić Anita
Testületi szerző: 30th International Symposium on Analytical and Environmental Problems
Dokumentumtípus: Könyv része
Megjelent: University of Szeged Szeged 2024
Sorozat:Proceedings of the International Symposium on Analytical and Environmental Problems 30
Kulcsszavak:Gyógyszerkémia
Tárgyszavak:
Online Access:http://acta.bibl.u-szeged.hu/85753
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100 1 |a Dimitrijević Marija 
245 1 0 |a Microwave synthesis of disubstituted pyrrolidine-2,5-dione derivatives  |h [elektronikus dokumentum] /  |c  Dimitrijević Marija 
260 |a University of Szeged  |b Szeged  |c 2024 
300 |a 335-339 
490 0 |a Proceedings of the International Symposium on Analytical and Environmental Problems  |v 30 
520 3 |a Succinimide (pyrrolidine-2,5-dione) derivatives are organic compounds with a broad spectrum of pharmacological activities. Analogs of this cyclic ureide are well-known and comercially available anticonvulsants (ethosuccinimide, metosuccinimide and fensuccinimide), antipsychotics, sedatives, anticancer and antiviral agents. In this paper, using a modified microwave procedure, three succinimide derivatives were synthetized and completely structurally characterized by determination of melting points, as well as FT-IR/ATR, 1H NMR, 13C NMR and elemental analysis. The influence of chemical structure on the pharmacological activity of succinimide derivatives was evaluated using the pioneering "rule of five", Veber, Egan, and Ghose’s empirical criteria, as well as using different in silico methods. Obtained values of molecular descriptors were compared with the characteristic values for reference drugs such as methosuccinimide and ethosuccinimide. Calculated molecular descriptors suggest that the investigated compounds fulfill necessary empirical criteria which qualify them as interesting drug candidates. The obtained descriptors indicate a high degree of gastrointestinal absorption (98%) of the synthesized succinimide derivatives. They are expected to successfully pass through the blood-brain barrier due to the adequate lipophilicity. 
650 4 |a Természettudományok 
650 4 |a Kémiai tudományok 
695 |a Gyógyszerkémia 
700 0 2 |a Gak Simić Kristina  |e aut 
700 0 2 |a Mašulović Aleksandra  |e aut 
700 0 2 |a Matović Luka  |e aut 
700 0 2 |a Lađarević Jelena  |e aut 
700 0 2 |a Banjac Nebojša  |e aut 
700 0 2 |a Trišović Nemanja  |e aut 
700 0 2 |a Lazić Anita  |e aut 
711 |a 30th International Symposium on Analytical and Environmental Problems  |c Szeged  |d 2024. október 7-8. 
856 4 0 |u http://acta.bibl.u-szeged.hu/85753/1/proceedings_of_isaep_2024_335-339.pdf  |z Dokumentum-elérés