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Synthesis, cytostatic and anti-viral activity evaluation of the novel acyclic nucleoside analogues containing a sterically constrained (Z)-4-amino-2-butenyl moiety (CROSBI ID 168622)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Wittine, Karlo ; Benci, Krešimir ; Kraljević Pavelić, Sandra ; Pavelić, Krešimir ; Bratulić, Siniša ; Hock, Karlo ; Balzarini, Jan ; Mintas, Mladen Synthesis, cytostatic and anti-viral activity evaluation of the novel acyclic nucleoside analogues containing a sterically constrained (Z)-4-amino-2-butenyl moiety // Medicinal chemistry research, 20 (2011), 3; 280-287. doi: 10.1007/s00044-010-9318-1

Podaci o odgovornosti

Wittine, Karlo ; Benci, Krešimir ; Kraljević Pavelić, Sandra ; Pavelić, Krešimir ; Bratulić, Siniša ; Hock, Karlo ; Balzarini, Jan ; Mintas, Mladen

engleski

Synthesis, cytostatic and anti-viral activity evaluation of the novel acyclic nucleoside analogues containing a sterically constrained (Z)-4-amino-2-butenyl moiety

A series of the novel pyrimidine (3-6) and purine (12-15, 18-21) acyclic nucleoside analogues in which the sugar moiety was replaced by a sterically constrained Z-4-amino-, 4-aminohydrochloride-2-butenyl, or aliphatic 4-aminohydrochloride-2-butyl moiety were synthesized and evaluated for their antiviral and cytostatic activity potency. Cytostatic evaluation of the novel compounds on selected panel of human tumour cell lines showed that the majority of compounds exerted a non-specific antiproliferative effect at the highest tested concentration (i.e. 1 x 10-4 M) against all cell lines. Nevertheless, a rather moderate but selective antiproliferative effects on HeLa cell cultures in comparison to normal fibroblasts WI 38, was observed for compounds 15 and 21. No antiviral activity was observed, except for compounds 3, 4 and 5 that showed anti-HIV activity at 50% effective concentration ranging between 29 and 96 µM.

acyclic nucleoside analogues; purine and pyrimidine derivatives; cytostatic activity; antiviral activity

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Podaci o izdanju

20 (3)

2011.

280-287

objavljeno

1054-2523

10.1007/s00044-010-9318-1

Povezanost rada

Kemija, Temeljne medicinske znanosti

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