Pregled bibliografske jedinice broj: 761803
Derivati purinskih bioizostera i pirimidina s 1, 2, 3- triazolom kao farmakoforom
Derivati purinskih bioizostera i pirimidina s 1, 2, 3- triazolom kao farmakoforom // XXIV. hrvatski skup kemičara i kemijskih inženjera / Ukić, Šime ; Bolanča, Tomislav (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2015. str. 185-185 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 761803 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Derivati purinskih bioizostera i pirimidina s 1, 2, 3- triazolom kao farmakoforom
(1, 2, 3-triazole pharmacophore-based derivatives of purine bioisosteres and pyrimidines)
Autori
Gregorić, Tomislav ; Bistrović, Andrea ; Tomljenović Paravić, Andrea ; Sedić, Mirela ; Kraljević Pavelić, Sandra ; Gazivoda Kraljević, Tatjana ; Raić-Malić, Silvana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
ISBN
978-953-6894-54-3
Skup
XXIV. hrvatski skup kemičara i kemijskih inženjera
Mjesto i datum
Zagreb, Hrvatska, 21.04.2015. - 24.04.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
1 ; 2 ; 3-triazoli ; purinski bioizosteri ; cikloadicija alkina i azida ; citostatska djelovanja
(1 ; 2 ; 3-triazoles ; purine bioisosteres ; alkyne-azide cycloaddition ; cytostatic activity)
Sažetak
Introduction of a 1, 2, 3-triazole ring into nucleosides to improve their bioactivity for antitumor or antiviral applications has become wide spread. The click chemistry reactions of nucleosides and nucleotides have found wide application in lead identification and lead optimization procedures in drug design. The 1, 2, 3- triazole unit may be considered as a surrogate of the amide group because it has H-bond acceptor capacity, distance between substituents and dipolar properties similar to the peptide bond. Keeping into consideration the biological potency of 1, 2, 3-triazolo-nucleosides [1, 2] and in our continuous endeavor toward the synthesis of pharmacologically active molecules, we designed the synthesized 1, 2, 3-triazole embedded N- heterocycles in order to evalute their cytostatic activities. The target regioselective 1, 4- disubstituted 1, 2, 3-triazole derivatives were prepared by the Cu-catalyzed alkyne-azide cycloaddition (CuAAC). Linear alkyl chain, substituted aromatic moiety and cyclopropyl ring were introduced as alkynyl substituents at C-5 and N-3 of pyrimidine core using palladium catalysed cross-coupling Sonogashira reaction. Evaluations of cytostatic activities of the synthesyzed compounds are currently underway.
Izvorni jezik
Hrvatski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2013-11-5596 - Sinteza i citostatska ispitivanja biblioteke novih dušikovih heterocikla (SCIENcENTRY) (Raić-Malić, Silvana, HRZZ - 2013-11) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Silvana Raić-Malić
(autor)
Andrea Bistrović
(autor)
Tatjana Gazivoda Kraljević
(autor)
Andrea Tomljenović Paravić
(autor)
Mirela Sedić
(autor)
Sandra Kraljević Pavelić
(autor)
Tomislav Gregorić
(autor)