| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1364973 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
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, IC50 = 2.2 μM), against MCF-7, that is, hormone-dependent breast cancer cell line, showed no toxicity to human erythrocytes even at higher concentrations (100 μg/ml, 258 μM). While, indanones 11, 12 and 14 showed toxicities to erythrocytes at higher concentrations.
Graphical abstractGallic acid-based indanone derivatives have been synthesised. Indanones 10, 11, 12 and 14 showed potent anticancer activity (IC50 = 0.022–2.2 μM) against human cancer cell lines. The most active indanone against MCF-7, that is, hormone-dependent breast cancer cell line (10, IC50 = 2.2 μM) showed no toxicity to human erythrocytes even at higher concentrations (100 μg/ml, 258 μM). While, some of the indanones exhibited toxicity to erythrocytes at higher concentrations. Gallic acid-based indanones may further be optimised as better anticancer agents with low toxicity.Figure optionsDownload full-size imageDownload as PowerPoint slide
