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Steroid-linked nitrogen mustards as potential anticancer therapeutics: a review. | LitMetric

Steroid-linked nitrogen mustards as potential anticancer therapeutics: a review.

J Steroid Biochem Mol Biol

Department of Pharmacy, Jahangirnagar University, Savar, Dhaka 1342, Bangladesh. Electronic address:

Published: September 2013

AI Article Synopsis

  • Nitrogen mustards are reactive cancer drugs that damage DNA but can cause serious side effects due to their lack of selectivity.
  • By attaching these nitrogen mustards to steroid hormones that target specific receptors, researchers aim to develop more selective and less toxic cancer treatments.
  • The review highlights the synthesis and testing of steroid-nitrogen mustard hybrids, particularly those with aromatic modifications linked by ester functions, which show promise for improved effectiveness and reduced toxicity.

Article Abstract

Nitrogen mustards, an important class of drugs for cancer therapy, are known as DNA alkylating agents. The nitrogen mustards are highly reactive and, as a consequence, lack of selectivity and produce several adverse side effects. In order to minimize these undesirable effects, the attachment of nitrogen mustards to a steroidal hormone with affinity for its receptor can lead to highly selective and less toxic antineoplastic therapeutics. This review will focus on the design, synthesis and evaluation of such steroid-nitrogen mustard hybrids as antineoplastic agents. Among these compounds, modified steroids with aromatic nitrogen mustards linked by an ester function were found to have better DNA alkylating properties, improved selectivity as well as low toxicity. This article is part of a Special Issue entitled "Synthesis and biological testing of steroid derivatives as inhibitors".

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Source
http://dx.doi.org/10.1016/j.jsbmb.2013.05.004DOI Listing

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