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Novel amidino substituted 2-phenylbenzothiazoles : Synthesis, antitumor evaluation in vitro and acute toxicity testing in vivo (CROSBI ID 157423)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Racané, Livio ; Kralj, Marijeta ; Šuman, Lidija ; Stojković, Ranko ; Tralić-Kulenović, Vesna ; Karminski-Zamola, Grace Novel amidino substituted 2-phenylbenzothiazoles : Synthesis, antitumor evaluation in vitro and acute toxicity testing in vivo // Bioorganic & medicinal chemistry, 18 (2010), 3; 1038-1044. doi: 10.1016/j.bmc.2009.12.054

Podaci o odgovornosti

Racané, Livio ; Kralj, Marijeta ; Šuman, Lidija ; Stojković, Ranko ; Tralić-Kulenović, Vesna ; Karminski-Zamola, Grace

engleski

Novel amidino substituted 2-phenylbenzothiazoles : Synthesis, antitumor evaluation in vitro and acute toxicity testing in vivo

The efficient synthesis of new bis-substituted nitro-amidino, amino-amidino (10a, 10b - 13a, 13b) and previously prepared diamidino 2-phenyl-benzothiazoles (9a, 9b) is described. The compounds 11a and 11b were prepared by recently developed methodology of the key precursors in zwitterionic form 8a and 8b with 4-nitrobenzoylchloride in a very good yield (70 %). All compounds except diamidino-substituted 2-phenylbenzothiazole 9a show exceptionally prominent tumor cell-growth inhibitory activity and cytotoxicity, whereby the special selectivity of amino-amidine 2-phenylbenzothiazole 12a towards MCF-7 and H 460 cells makes this compound a prospective lead compound that should be further evaluated in animal models. All in vivo tested compounds (12a, 12b, 13a and 13b) are absorbed from mice gastrointestinal system. LD50 are between 67.33 and 696.2 mg/kg body weight (OECD/EPA toxicity categories 2-3).

nitro-amidino- ; amino-amidino- and diamidino-substituted

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Podaci o izdanju

18 (3)

2010.

1038-1044

objavljeno

0968-0896

10.1016/j.bmc.2009.12.054

Povezanost rada

Kemija, Biologija, Temeljne medicinske znanosti

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