| Literature DB >> 15914009 |
Seikou Nakamura1, Mutsuo Kozuka, Kenneth F Bastow, Harukuni Tokuda, Hoyoku Nishino, Madoka Suzuki, Jin Tatsuzaki, Susan L Morris Natschke, Sheng-Chu Kuo, Kuo-Hsiung Lee.
Abstract
2-Phenyl-4-quinolone and 9-oxo-9,10-dihydroacridine derivatives were synthesized and screened as potential antitumor promoters by examining the ability of the compounds to inhibit Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells. Interestingly, compounds 14, 15, and 17 showed similar inhibitory effects (89-92%, 66-69%, and 24-29% at 1000, 500, and 100 mol ratio to TPA, respectively) against EBV-EA with potencies comparable to those of glycyrrhetic acid, a known natural antitumor-promoter.Entities:
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Year: 2005 PMID: 15914009 DOI: 10.1016/j.bmc.2005.04.078
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641