4.7 Article

Synthesis of amide and urea derivatives of benzothiazole as Raf-1 inhibitor

期刊

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
卷 43, 期 7, 页码 1519-1524

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2007.10.008

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benzothiazole derivatives; antiproliferative; Raf-1 activity

资金

  1. National Research Foundation of Korea [R01-2008-000-11354-0, 2006-02662] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A series of amide and urea derivatives of benzothiazole have been synthesized and evaluated for their antiproliferative profile in human SK-Hep-1 (liver), MDA-MB-231 (breast), and NUGC-3 (gastric) cell lines. Among them, compounds 1-2, 16-18, 23, and 25-26 had potent to moderate inhibitory activities. Further these compounds were investigated for their ability to inhibit Raf-1 activity. (c) 2007 Elsevier Masson SAS. All rights reserved.

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