Pregled bibliografske jedinice broj: 375718
Synthesis and Bioevaluation of 5-Fluorouracil Derivatives
Synthesis and Bioevaluation of 5-Fluorouracil Derivatives // Znanstveni skup hrvatskog društva za biokemiju i molekularnu biologiju, Knjiga sažetaka / Strelec, Ivica ; Glavaš-Obrovac, Ljubica (ur.).
Zagreb: Hrvatsko društvo za biokemiju i molekularnu biologiju (HDBMB), 2008. str. 142-142 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 375718 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and Bioevaluation of 5-Fluorouracil Derivatives
Autori
Žakić, Željka ; Saftić, Dijana ; Župančić, Nataša ; Glavaš-Obrovac, Ljubica ; Žinić, Biserka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Znanstveni skup hrvatskog društva za biokemiju i molekularnu biologiju, Knjiga sažetaka
/ Strelec, Ivica ; Glavaš-Obrovac, Ljubica - Zagreb : Hrvatsko društvo za biokemiju i molekularnu biologiju (HDBMB), 2008, 142-142
ISBN
978-953-95551-2-0
Skup
Congress of the Croatian Society of Biochemistry and Molecular Biology HDBMB 2008
Mjesto i datum
Osijek, Hrvatska, 17.09.2008. - 20.09.2008
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
5-Fluorouracil; N-Sulfonyl Derivatives; Reversed Nucleosides
Sažetak
As a part of research in our laboratories to develop novel anticancer agents, we have pursuing the synthesis of 1-sulfonyl-5-fluorouracil derivatives and “ reversed” nucleosides containing 5-fluorouracil base. The present work describes the coupling of sulfonyl chlorides or suitable activated sugar derivative with 5-fluorouracil base, using silyl method or condensation in presence of sodium hydride. The new derivatives were tested for their antiproliferative and cytotoxic effects on the growth of 6 different human tumor cell lines (cervical adenocarcinoma HeLa, laryngeal carcinoma HEp-2, pancreatic carcinoma MIAPaCa2, colon carcinoma HT-29, CaCo2, poorly differentiated cells from lymph node metastasis of colon carcinoma SW-620, and breast carcinoma MCF-7) and normal human fibroblasts WI38 in a parallel with 5-fluorouracil, as a standard antitumor drug. Cell lines were incubated with four 10-fold dilutions (10-8 to 10-4 M). After 72 hours of incubation the cell growth rate was evaluated using the MTT assay. Novel compounds displayed similar cell growth inhibition pattern in regard to structure similarity with 5-fluorouracil. The most pronounced growth inhibitory effect of FUTS and FUMS applied in all test concentration was observed on MIAPCa2 cells. Both sulfonyl compounds applied in the highest concentration (10-4 M) inhibited MIAPaCa2 cell growth for more than 80%. At the same time, maximal inhibitory capacity of 5-fluorouracil against the same cell line was 68%. In comparison with cytotoxicity of novel compounds, 5-fluorouracil was significantly more toxic (2-fold at the highest concentration applied) against normal human cells.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982914-2935 - Sinteza novih biološki aktivnih derivata nukleobaza i nukleotida (Žinić, Biserka, MZOS ) ( CroRIS)
219-0982914-2176 - Mehanizam bioloških učinaka novih malih molekula na stanice tumora čovjeka (Glavaš Obrovac, Ljubica, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Željka Ban
(autor)
Dijana Pavlović Saftić
(autor)
Biserka Žinić
(autor)
Ljubica Glavaš Obrovac
(autor)