| Literature DB >> 12213462 |
Junko Ishida1, Hironori Ohtsu, Yoko Tachibana, Yuka Nakanishi, Kenneth F Bastow, Masahiro Nagai, Hui-Kang Wang, Hideji Itokawa, Kuo-Hsiung Lee.
Abstract
Fifty-eight curcumin analogues were prepared and evaluated for in vitro cytotoxicity against a panel of human tumor cell lines. Compound was the most potent analogue against several cell lines, including HOS (bone cancer) and 1A9 (breast cancer), with ED50 values of 0.97 and <0.63 microg/mL, respectively.Entities:
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Year: 2002 PMID: 12213462 DOI: 10.1016/s0968-0896(02)00249-3
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641