Pregled bibliografske jedinice broj: 650840
The Novel [4, 5-e][1, 3]Diazepine-4, 8-dione and Acyclic Carbamoyl Imino-Ureido Derivatives of Imidazole : Synthesis, Anti-Viral and Anti-Tumor Activity Evaluations
The Novel [4, 5-e][1, 3]Diazepine-4, 8-dione and Acyclic Carbamoyl Imino-Ureido Derivatives of Imidazole : Synthesis, Anti-Viral and Anti-Tumor Activity Evaluations // Molecules, 18 (2013), 11; 13385-13397 doi:10.3390/molecules181113385 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 650840 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The Novel [4, 5-e][1, 3]Diazepine-4, 8-dione and Acyclic Carbamoyl Imino-Ureido Derivatives of Imidazole : Synthesis, Anti-Viral and Anti-Tumor Activity Evaluations
Autori
Wittine, Karlo ; Poljak, Kristina ; Kovač, Matea ; Makuc, Damjan ; Plavec, Janez ; Balzarini, Jan ; Martinović, Tamara ; Kraljević Pavelić, Sandra ; Pavelić, Krešimir ; Mintas, Mladen
Izvornik
Molecules (1420-3049) 18
(2013), 11;
13385-13397
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
imidazole; [4; 5-e][1; 3]diazepine; anti-RSV; anti-tumor
Sažetak
In the present paper, we report on the synthesis, and in vitro antiviral and cytostatic activities of a series of novel imidazole[4, 5-e][1, 3]diazepine-4, 8-dione (compounds 9–11) and acyclic carbamoyl imino-ureido imidazole (compounds 12 and 13) derivatives. These new type of chemical entities showed no significant activity on the broad spectrum of DNA and RNA viruses. Results of antiproliferative assays performed on a panel of selected human tumor cell lines revealed that only compounds 1 and 5 showed moderate and selective cytostatic effect against HeLa cells (IC50 = 24 and 32 µM) with no concomitant cytotoxic effects on human normal fibroblasts (BJ). Importantly, an imidazole derivative containing a pyrrolidine moiety linked via an ethylenic spacer (3) showed a selective cytostatic effect toward cervical carcinoma (HeLa) cells (IC50 = 9.5 µM) with no apparent cytotoxicity on human normal fibroblasts (BJ). This compound can be therefore considered as a potential anti-tumor lead compound for further synthetic structure optimization.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biotehnologija
POVEZANOST RADA
Projekti:
125-0982464-2922 - RAZVOJ NOVIH PROLIJEKOVA I LIJEKOVA PROTIV VIRUSA I RAKA (Mintas, Mladen, MZOS ) ( CroRIS)
335-0000000-3532 - Uloga IGF2 i signalni putovi nizvodno u karcinomima pluća čovjeka (Peter-Katalinić, Jasna, MZOS ) ( CroRIS)
335-0982464-2393 - Molekularna obilježja miofibroblasta Dupuytrenove bolesti (Pavelić, Krešimir, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Krešimir Pavelić
(autor)
Mladen Mintas
(autor)
Sandra Kraljević Pavelić
(autor)
Karlo Wittine
(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
- MEDLINE