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Characterisation of radicals formed by the triazine 1,4-dioxide hypoxia-activated prodrug, SN30000

Anderson, Robert F.; Yadav, Pooja; Patel, Deepa; Reynisson, Jóhannes; Tipparaju, Smitha R.; Guise, Christopher P.; Patterson, Adam V.; Denny, William A.; Maroz, Andrej; Shinde, Sujata S.; Hay, Michael P.

Authors

Robert F. Anderson

Pooja Yadav

Deepa Patel

Smitha R. Tipparaju

Christopher P. Guise

Adam V. Patterson

William A. Denny

Andrej Maroz

Sujata S. Shinde

Michael P. Hay



Abstract

The radical species underlying the activity of the bioreductive anticancer prodrug, SN30000, have been identified by electron paramagnetic resonance and pulse radiolysis techniques. Spin-trapping experiments indicate both an aryl-type radical and an oxidising radical, trapped as a carbon-centred radical, are formed from the protonated radical anion of SN30000. The carbon-centred radical, produced upon the one-electron oxidation of the 2-electron reduced metabolite of SN30000, oxidises 2-deoxyribose, a model for the site of damage on DNA which leads to double strand breaks. Calculations using density functional theory support the assignments made.

Citation

Anderson, R. F., Yadav, P., Patel, D., Reynisson, J., Tipparaju, S. R., Guise, C. P., …Hay, M. P. (in press). Characterisation of radicals formed by the triazine 1,4-dioxide hypoxia-activated prodrug, SN30000. Organic and Biomolecular Chemistry, 12(21), 3386-3392. https://doi.org/10.1039/c4ob00236a

Journal Article Type Article
Acceptance Date Apr 9, 2014
Online Publication Date Apr 10, 2014
Deposit Date Jun 8, 2023
Journal Org. Biomol. Chem.
Print ISSN 1477-0520
Electronic ISSN 1477-0539
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 12
Issue 21
Pages 3386-3392
DOI https://doi.org/10.1039/c4ob00236a
Keywords Organic Chemistry; Physical and Theoretical Chemistry; Biochemistry
Additional Information : This document is CrossCheck deposited; : Supplementary Information; : The Royal Society of Chemistry has an exclusive publication licence for this journal; OPEN ACCESS: The accepted version of this article will be made freely available after a 12 month embargo period; : Received 31 January 2014; Accepted 9 April 2014; Accepted Manuscript published 10 April 2014; Advance Article published 16 April 2014; Version of Record published 7 May 2014