Design and synthesis of ERα/ERβ selective coumarin and chromene derivatives as potential anti-breast cancer and anti-osteoporotic agents

• Published in: RSC advances 2014, Vol.4 (17), p.8828-8845
• Main Authors: Hussain, M. Kamil, Ansari, M. Imran, Yadav, N., Gupta, Puneet K., Gupta, A. K., Saxena, R., Fatima, I., Manohar, M., Kushwaha, P., Khedgikar, V., Gautam, J., Kant, Ruchir, Maulik, P. R., Trivedi, R., Dwivedi, A., Kumar, K. Ravi, Saxena, A. K., Hajela, K.
• Format: Article
• Language: English
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/C3RA45749D

Several new coumarin and chromene prototype derivatives have been synthesised and evaluated for their ER alpha and ER beta selective activity. Coumarin prototype compounds 18 & 19 were found to be ER alpha selective and the most active, exhibiting potential antiproliferative activity against both ER +ve & ER -ve breast cancer cell lines. The surprise finding of the series, however, are the novel prototype III chromenes 45 & 46, with aroyl substitution at the 6 super(th) position. Both the compounds have shown potent antiproliferative activity against both the breast cancer cell lines, promote alkaline phosphatase activity, enhance osteoblast mineralization in vitro, significantly decrease ERE-ER alpha dependent transactivation and induce ER beta activity. This specific upregulation of ER beta isoform activity of compound 45 may be responsible for the antiosteoporotic activity at picomolar concentration. In addition, both the compounds were also devoid of any estrogenic activity, which correlates to their antiestrogenic behaviour in the two breast cancer cell lines. Assessment of selectivity using specific SiRNAs for ER alpha and ER beta revealed that most of the compounds showed ER alpha and ER beta -mediated action, except compound 28, which showed selectivity to ER alpha only. Computational docking analysis of active compounds 18 and 45 was conducted to correlate the interaction with the two receptors and it was found that the docked conformations of the coumarin prototype, compound 18 at ER alpha and ER beta active sites were more or less superimposable on each other. However, the unique orientation of the aminoalkoxy side chain of novel chromene (prototype III) compound 45 in the ER beta binding cavity may be responsible for its potential biological response.