Bismuth nitrate-induced novel nitration of estradiol: An entry to new anticancer agents

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Abstract

Direct nitration of estradiol was carried out using metal nitrates on solid surfaces under mild condition, and a combination of bismuth nitrate pentahydrate impregnated KSF clay was found to be the best reagent to synthesize 2- and 4-nitroestradiol effectively. Furthermore, various basic side chains were introduced, through O-linker at C-3, to these nitroestradiols. The ability of these derivatives to cause cytotoxicity in Estrogen Receptor (ER)-positive and ER-negative breast cancer cell lines, as well as cancer cell lines of other origins, was examined. Qualitative structure activity relationship (SAR) has also been studied. We found that a basic side chain containing either a piperidine or morpholine ring, when conjugated to 2-nitroestradiol, was particularly effective at causing cytotoxicity in each of the cancer cell lines examined. Surprisingly, this effective cytotoxicity was even seen in ER-negative breast cancer cells. © 2014 Published by Elsevier Masson SAS.

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Bandyopadhyay, D., Rivera, G., Sanchez, J. L., Rivera, J., Granados, J. C., Guerrero, A. M., … Banik, B. K. (2014). Bismuth nitrate-induced novel nitration of estradiol: An entry to new anticancer agents. European Journal of Medicinal Chemistry, 82, 574–583. https://doi.org/10.1016/j.ejmech.2014.06.010

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