Nitroreductase-activated nitric oxide (NO) prodrugs

  • Bioorg Med Chem Lett. 2013 Nov 1;23(21):5964-7. doi: 10.1016/j.bmcl.2013.08.066.
Kavita Sharma  1 Kundan Sengupta Harinath Chakrapani
Affiliations
  • 1. Department of Chemistry, Indian Institute of Science Education and Research Pune, Pune, Maharashtra, India.
Abstract

Due to the involvement of nitric oxide (NO) in numerous and diverse physiological processes, site-directed delivery of therapeutic NO in order to minimize unwanted side-effects is necessary. O(2)-(4-Nitrobenzyl) diazeniumdiolates are designed as substrates for Escherichia coli nitroreductase (NTR), an enzyme that is frequently used to facilitate directed delivery of cytotoxic species to cancers. O(2)-(4-Nitrobenzyl) diazeniumdiolates are found to be stable in aqueous buffer but are metabolized by NTR to produce NO. A cell viability assay revealed that cytotoxic effects of O(2)-(4-nitrobenzyl)1-(2-methylpiperidin-1-yl)diazen-1-ium-1,2-diolate (4b) towards two Cancer cell lines is significantly enhanced in the presence of NTR suggesting the potential for use of this compound in nitric oxide-based directed prodrug therapy.

Keywords
Diazeniumdiolate; Directed prodrug therapy; Nitric oxide; Nitroreductase; Prodrug.
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