Krištafor, Svjetlana; Gazivoda Kraljević, Tatjana; Makuc, Damjan; Plavec, Janez; Šuman, Lidija; Kralj, Marijeta; Raić-Malić, Silvana
(2009)
Synthesis, Structural Studies and Antitumoral Evaluation of C-6 Alkyl and Alkenyl Side Chain Pyrimidine Derivatives.
Molecules, 14
(12).
pp. 4866-4879.
ISSN 1420-3049
Abstract
The synthetic route for introduction of fluorophenylalkyl (compounds 5, 7, 14 and 15) and fluorophenylalkenyl (compounds 4E and 13) side chains at C-6 of the pyrimidine nucleus involved the lithiation of the pyrimidine derivatives 1, 2 and 11 and subsequent nucleophilic addition or substitution reactions of the organolithium intermediate thus obtained with 2-fluorophenylacetone, 4-fluoroacetophenone or ethyl 4-fluorobenzoate as electrophiles. The structures of novel compounds were confirmed by 1H , 19F- and 13C-NMR and MS. Compounds 8 and 10 containing unsaturated fluorophenylalkyl side chains showed better inhibitory effect than their saturated fluorophenylalkylated pyrimidine counterparts 7 and 9. A conformational study based on NOE enhancements showed the importance of the double bond and substitution in the side chain for the conformational preferences in relation to inhibitory activity. Among all tested compounds, C-5 furyl (12) and phenyl (13 and 15) substituted pyrimidine derivatives showed significant cytostatic activities against all tested tumor cell lines.
Item Type: |
Article
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Uncontrolled Keywords: |
C-6 alkyl and alkenyl pyrimidine derivatives ; NMR conformational analysis ; cytostatic activity evaluation |
Subjects: |
NATURAL SCIENCES > Chemistry |
Divisions: |
Division of Molecular Medicine |
Projects: |
Project title | Project leader | Project code | Project type |
---|
Uloga različitih mehanizama odgovora stanica na terapiju oštećenjem DNA- | Marijeta Kralj | 098-0982464-2514 | MZOS | Razvoj i primjena novih molekula u pozitron-emisijskoj tomografiji (PET)- | Silvana Raić-Malić | 125-0982464-2925 | MZOS |
|
Depositing User: |
Marijeta Kralj
|
Date Deposited: |
24 Feb 2020 15:22 |
URI: |
http://fulir.irb.hr/id/eprint/5311 |
DOI: |
10.3390/molecules14124866 |
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5311
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