| Literature DB >> 18586491 |
Hari Om Saxena1, Uzma Faridi, Suchita Srivastava, J K Kumar, M P Darokar, Suaib Luqman, C S Chanotiya, Vinay Krishna, Arvind S Negi, S P S Khanuja.
Abstract
Gallic acid-based indanone derivatives have been synthesised. Some of the indanones showed very good anticancer activity in MTT assay. Compounds 10, 11, 12 and 14 possessed potent anticancer activity against various human cancer cell lines. The most potent indanone (10, IC(50)=2.2 microM), against MCF-7, that is, hormone-dependent breast cancer cell line, showed no toxicity to human erythrocytes even at higher concentrations (100 microg/ml, 258 microM). While, indanones 11, 12 and 14 showed toxicities to erythrocytes at higher concentrations.Entities:
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Year: 2008 PMID: 18586491 DOI: 10.1016/j.bmcl.2008.06.039
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823