Pregled bibliografske jedinice broj: 1195061
Green Synthesis And Antitumor Evaluations Of Novel Racemic And Optically Pure Aryl-Substituted Purine Bioisosteres
Green Synthesis And Antitumor Evaluations Of Novel Racemic And Optically Pure Aryl-Substituted Purine Bioisosteres // ICNTC ( “8th International Conference on New Trends in Chemistry”)
Famagusta, Cipar, 2022. str. 1-2 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1195061 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Green Synthesis And Antitumor Evaluations Of Novel
Racemic And Optically Pure Aryl-Substituted Purine
Bioisosteres
Autori
Piškor, Martina ; Kraljević Pavelić, Sandra ; Grbčić, Petra ; Sedić, Mirela ; Majerić Elenkov, Maja ; Raić-Malić, Silvana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
ICNTC ( “8th International Conference on New Trends in Chemistry”)
Mjesto i datum
Famagusta, Cipar, 15.05.2022. - 18.05.2022
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
purin, enantiomer, enantioselektivno, halohidrin dehalogenaza
(purine, azido alcohols, enantiomers, halohydrin dehalogenase)
Sažetak
Enzymes, receptors, and other binding molecules in biological processes can recognize enantiomers as different molecular entities, consequently, using a single pure enantiomer instead of a racemate can enhance the effectiveness and safety of the treatment [1]. The method for the synthesis of enantiopure or highly enantio-enriched compounds is asymmetric organometallic catalysis, which has been recently replaced by biocatalysis. An important example of enzymatic biocatalysis is the nucleophilic opening of epoxy rings with sodium azide catalysed by halohydrin dehalogenase (HHDHs) [2]. Enantiomerically pure β-azido alcohols are very important building blocks in the synthesis of 1, 2, 3-triazole derivatives [3]. As part of our research on developing multi-target small molecule anticancer agents, we designed, synthesized, and biologically evaluated a series of 66 novel hydroxyl aryl-substituted N-heterocycle derivatives. A series of 50 racemic and 16 optical pure 1, 4-disubstituted 1, 2, 3-triazoles were synthesized by the copper(I)-catalyzed Huisgen 1, 3-dipolar cycloaddition of terminal alkynyl derivatives of purine and purine isosteres and aryl-substituted 1, 2-azido alcohols under environmentally friendly ultrasound irradiation. The synthesis and antitumor effects of all derivatives will be presented.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-4682 - Novi spojevi temeljeni na bioizosterima purina za ispitivanje njihovih antitumorskih i antipatogenih djelovanja (PurBioCaPa) (Raić-Malić, Silvana, HRZZ - 2018-01) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Maja Majerić Elenkov
(autor)
Mirela Sedić
(autor)
Petra Grbčić
(autor)
Sandra Kraljević Pavelić
(autor)
Martina Piškor
(autor)
Silvana Raić-Malić
(autor)