Pregled bibliografske jedinice broj: 486543
Syntheses and antitumor evaluation of C(6)-isobutyl- and C(6)-isobutenyl-substituted pyrimidines, and dihydropyrrolo[1,2-c]pyrimidine-1,3-diones
Syntheses and antitumor evaluation of C(6)-isobutyl- and C(6)-isobutenyl-substituted pyrimidines, and dihydropyrrolo[1,2-c]pyrimidine-1,3-diones // Chemistry & biodiversity, 8 (2011), 8; 1455-1469 doi:10.1002/cbdv.201000202 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 486543 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Syntheses and antitumor evaluation of C(6)-isobutyl- and C(6)-isobutenyl-substituted pyrimidines, and dihydropyrrolo[1,2-c]pyrimidine-1,3-diones
Autori
Krištafor, Svjetlana ; Gazivoda Kraljević, Tatjana ; Ametamey, Simon M. ; Cetina, Mario ; Ratkaj, Ivana ; Tandara Haček, Romana ; Kraljević Pavelić, Sandra ; Raić-Malić, Silvana
Izvornik
Chemistry & biodiversity (1612-1872) 8
(2011), 8;
1455-1469
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
C-6 isobutyl and isobutenyl substituted pyrimidine derivatives ; cytostatic evaluation ; apoptosis ; X-ray crystal structure analysis
Sažetak
A growing body of evidence supports that pyrimidine derivatives, in which the sugar residues have been replaced by acyclic side chains, might be developed as promising anticancer agents that interfere with tumor cell proliferation, survival, and metastatic formation. In this work, we prepared novel pyrimidines bearing i-Bu (i.e., 3, 4, and 7–9) and isobutenyl (i.e., 5 and 10) side chains at C(6) and examined their in vitro effects on tumor cell lines. The dihydropyrrolo[1, 2-c]pyrimidin-1, 3-diones 6 and 11 were obtained as products of intramolecular cyclization, which occurred during the removal of Bn in 5 or MeO protecting groups in 10. Fluorination of 3 with diethylaminosulfur trifluoride (DAST) and then dehydrohalogenation of the resulting fluorinated derivative 4 afforded 6-isobut-2’-enyl pyrimidine derivative 5 with a C(2’)¼C(3’) bond. For the preparation of 6-isobut-1’-en-1-yl pyrimidine 10, a synthetic strategy involving acetylation of the 1, 3-diols was applied. Antitumor evaluation of compounds 3–11 showed that 2, 4-dimethoxypyrimidine containing 6-[(1, 3-dibenzyloxy)-2-hydroxy]methyl side chain, 3, exerted a strong antiproliferative effect on the studied tumor cell lines. Additionally, it was shown that the mechanism of antiproliferative effect of 3 in HeLa cells include early G2/M arrest and apoptosis, as well as a p53-independent S-phase arrest upon prolonged treatment.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-119-1193079-3069 - Novi organski i koordinacijski spojevi - sinteza i suodnos struktura-svojstvo (Kaitner, Branko, MZOS ) ( CroRIS)
MZOS-125-0982464-2925 - Razvoj i primjena novih molekula u pozitron-emisijskoj tomografiji (PET) (Raić-Malić, Silvana, MZOS ) ( CroRIS)
MZOS-335-0000000-3532 - Uloga IGF2 i signalni putovi nizvodno u karcinomima pluća čovjeka (Peter-Katalinić, Jasna, MZOS ) ( CroRIS)
MZOS-335-0982464-2393 - Molekularna obilježja miofibroblasta Dupuytrenove bolesti (Pavelić, Krešimir, MZOS ) ( CroRIS)
Ustanove:
Imunološki zavod d.d.,
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Sandra Kraljević Pavelić
(autor)
Ivana Ratkaj
(autor)
Svjetlana Krištafor
(autor)
Silvana Raić-Malić
(autor)
Romana Tandara-Haček
(autor)
Mario Cetina
(autor)
Tatjana Gazivoda Kraljević
(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
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)