Pregled bibliografske jedinice broj: 191949
Synthesis, spectroscopic characterization and biological activity of N-1-sulfonylcytosine derivatives
Synthesis, spectroscopic characterization and biological activity of N-1-sulfonylcytosine derivatives // Croatica chemica acta, 78 (2005), 2; 261-267 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 191949 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis, spectroscopic characterization and biological activity of N-1-sulfonylcytosine derivatives
Autori
Kašnar-Šamprec, Jelena ; Glavaš-Obrovac, Ljubica ; Pavlak, Marina ; Mihaljević, Ivan ; Mrljak, Vladimir ; Štambuk, Nikola ; Konjevoda, Paško ; Žinić, Biserka
Izvornik
Croatica chemica acta (0011-1643) 78
(2005), 2;
261-267
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
N-1-Sulfonylcytosine derivatives ; in vitro antiproliferative effect ; antitumor activity ; hematologic findings
Sažetak
Large scale preparation of N-1-sulfonylcytosine derivatives has been optimized. The best method was the condensation reaction of silylated cytosine (1) with p-toluenesulfonyl chloride in acetonitrile. Depending on the isolation procedure, 1-(p-toluenesulfonyl)cytosine 2 and 1- (p-toluenesulfonyl)cytosine hydrochloride 3 were isolated in 80 % and 75 % yield, respectively. The NMR evidence presented, shows that 2 appears as a common keto-amino tautomer in DMSO-d6 solution while its hydrochloride 3 forms exclusively rare keto-imino tautomer. N-1-Sulfonylcytosine derivatives 2 and 3 were investigated for possible cytotoxic activity on human normal fibroblasts (WI38), human pancreatic adenocarcinoma cells (MIAPaCa2), poorly differentiated cells from lymph node metastasis of colon carcinoma (SW-620), and human Burkitt lymphoma cells (Raji). MTT- cytotoxicity screens in human tissue culture cell lines showed that both of investigated compounds demonstrated antiproliferative activity in the different histological types of tumors. In comparison with 5-fluorouracil, some of N-1- sulfonylcytosine derivatives showed 10 times stronger activity, considering IC50. The inhibitory effect of the investigated derivatives on normal human cells was lower in comparison to antitumor effects. In addition to the antitumor effects, hematologic findings following the parenteral administration of substances were also investigated.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti
Napomena
Rad je kao poster prezentiran na skupu MMC2004, održanom od 10.-14.06.2004.g., Cavtat, Hrvatska ; uz međunarodnu recenziju objavljen u Knjizi sažetaka ; te na skupu The 19th Dubrovnik International Course & Conference on the Interfaces among Mathematics, Chemistry and Computer Sciences (MATH/CHEM/COMP 2004), održanom od 21-26.06.2004.g., Dubrovnik, Hrvatska, objavljen uz međunarodnu recenziju u Knjizi sažetaka / Ante Graovac, Biserka Pokrić, Vilko Smrečki, ur. ; Zagreb : Ruđer Bošković Institute , 2004.g., str. 32-32.
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Osijek,
Akademija medicinskih znanosti,
Medicinski fakultet, Osijek,
Sveučilište J. J. Strossmayera u Osijeku
Profili:
Jelena Kašnar-Šamprec
(autor)
Marina Pavlak
(autor)
Nikola Štambuk
(autor)
Biserka Žinić
(autor)
Ljubica Glavaš Obrovac
(autor)
Paško Konjevoda
(autor)
Vladimir Mrljak
(autor)
Ivan Mihaljević
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- Chemical Abstracts