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Synthesis and Antitumor Evaluation of Novel Derivatives of 6-Amino-2-phenylbenzothiazoles (CROSBI ID 100262)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Racane, Livio ; Stojković, Ranko ; Tralić-Kulenović, Vesna ; Karminski-Zamola, Grace Synthesis and Antitumor Evaluation of Novel Derivatives of 6-Amino-2-phenylbenzothiazoles // Molecules, 11 (2006), 5; 325-333. doi: 10.3390/11050325

Podaci o odgovornosti

Racane, Livio ; Stojković, Ranko ; Tralić-Kulenović, Vesna ; Karminski-Zamola, Grace

engleski

Synthesis and Antitumor Evaluation of Novel Derivatives of 6-Amino-2-phenylbenzothiazoles

Novel derivatives of 6-amino-2-phenylbenzothiazole bearing different substituents (amino, dimethylamino or fluoro) on the phenyl ring were prepared as the corresponding hydrochloride salts. 6-Nitro-2-(substituted-phenyl)benzothiazoles (1-6) were synthesized by condensation reactions of substituted benzaldehydes with 2-amino-5-nitrothiophenol. Nitro derivatives were reduced to the amino derivatives with SnCl2/HCl. Water soluble hydrochloride salts of 6-amino-2-(substituted-phenyl)benzothiazole (13-19) were prepared using concentrated or gaseous HCl. Compounds 13-19 were found to exert cytostatic activities against malignant human cell lines: cervical (HeLa), breast (MCF-7), colon (CaCo-2), laryngeal carcinoma (Hep-2), and normal human fibroblast cell lines (WI38).

Benzothiazole synthesis ; antitumor activity

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Podaci o izdanju

11 (5)

2006.

325-333

objavljeno

1420-3049

10.3390/11050325

Povezanost rada

Kemija, Temeljne medicinske znanosti

Poveznice
Indeksiranost