Abstract
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.
Original language | English |
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Pages (from-to) | 1519-1524 |
Number of pages | 6 |
Journal | European Journal of Medicinal Chemistry |
Volume | 43 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2008 Jul |
Bibliographical note
Funding Information:This research was supported by the Korea Science and Engineering Foundation (KOSEF) grant (M10601000155) and Seoul R&BD Program (10541), Korea.
All Science Journal Classification (ASJC) codes
- Pharmacology
- Drug Discovery
- Organic Chemistry