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Electron transfer in N-hydroxyurea complexes with iron(III)
Redox behaviour of the iron(III) complex with the antitumour drug hydroxyurea was studied by cyclic voltammetry. The complex underwent a one-electron reduction, followed by an irreversible chemical reaction (EC mechanism) in which a ligand was released. In addition, it was found that the hydroxyurea...
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Published in: | European journal of medicinal chemistry 2005, Vol.40 (1), p.51-55 |
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creator | NIGOVIC, Biljana KUJUNDZIC, Nikola SANKOVIC, Kresimir |
description | Redox behaviour of the iron(III) complex with the antitumour drug hydroxyurea was studied by cyclic voltammetry. The complex underwent a one-electron reduction, followed by an irreversible chemical reaction (EC mechanism) in which a ligand was released. In addition, it was found that the hydroxyurea gave up an electron to iron(III) in solution. Differential-pulse voltammetry revealed an increase in the concentration of the generated iron(II) species. Electron paramagnetic resonance (EPR) spectroscopy studies of the oxidative degradation of hydroxyurea confirmed formation of the radical species H
2N–CO–NHO
.. Electrochemical data for iron(III) complexes of hydroxyurea and its structural analogue 3-ethylhydroxyurea, which also exhibits antitumour activity, show the same mechanism involved in the electron transfer. The observed redox properties indicate that hydroxyurea may interfere with electron transfer processes in biological systems after binding to iron-containing ribonucleotide reductase. |
doi_str_mv | 10.1016/j.ejmech.2004.09.012 |
format | article |
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2N–CO–NHO
.. Electrochemical data for iron(III) complexes of hydroxyurea and its structural analogue 3-ethylhydroxyurea, which also exhibits antitumour activity, show the same mechanism involved in the electron transfer. The observed redox properties indicate that hydroxyurea may interfere with electron transfer processes in biological systems after binding to iron-containing ribonucleotide reductase.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2004.09.012</identifier><identifier>PMID: 15642408</identifier><identifier>CODEN: EJMCA5</identifier><language>eng</language><publisher>Oxford: Elsevier Masson SAS</publisher><subject>Antineoplastic Agents - chemistry ; Biological and medical sciences ; Chemistry ; Coordination compounds ; Electrochemistry ; Electron Spin Resonance Spectroscopy ; Electron transfer ; EPR ; Exact sciences and technology ; Hydroxyurea ; Hydroxyurea - chemistry ; Inorganic chemistry and origins of life ; Iron - chemistry ; Iron(III) complexes ; Medical sciences ; Miscellaneous ; Oxidation-Reduction ; Pharmacology. Drug treatments ; Preparations and properties ; Voltammetry</subject><ispartof>European journal of medicinal chemistry, 2005, Vol.40 (1), p.51-55</ispartof><rights>2004 Elsevier SAS</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-4d7ea3b4946ee91e751a6e95db5b969099fa8f875c6e00a2d95b8bdfb19aff3f3</citedby><cites>FETCH-LOGICAL-c390t-4d7ea3b4946ee91e751a6e95db5b969099fa8f875c6e00a2d95b8bdfb19aff3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16446834$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15642408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>NIGOVIC, Biljana</creatorcontrib><creatorcontrib>KUJUNDZIC, Nikola</creatorcontrib><creatorcontrib>SANKOVIC, Kresimir</creatorcontrib><title>Electron transfer in N-hydroxyurea complexes with iron(III)</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>Redox behaviour of the iron(III) complex with the antitumour drug hydroxyurea was studied by cyclic voltammetry. The complex underwent a one-electron reduction, followed by an irreversible chemical reaction (EC mechanism) in which a ligand was released. In addition, it was found that the hydroxyurea gave up an electron to iron(III) in solution. Differential-pulse voltammetry revealed an increase in the concentration of the generated iron(II) species. Electron paramagnetic resonance (EPR) spectroscopy studies of the oxidative degradation of hydroxyurea confirmed formation of the radical species H
2N–CO–NHO
.. Electrochemical data for iron(III) complexes of hydroxyurea and its structural analogue 3-ethylhydroxyurea, which also exhibits antitumour activity, show the same mechanism involved in the electron transfer. The observed redox properties indicate that hydroxyurea may interfere with electron transfer processes in biological systems after binding to iron-containing ribonucleotide reductase.</description><subject>Antineoplastic Agents - chemistry</subject><subject>Biological and medical sciences</subject><subject>Chemistry</subject><subject>Coordination compounds</subject><subject>Electrochemistry</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Electron transfer</subject><subject>EPR</subject><subject>Exact sciences and technology</subject><subject>Hydroxyurea</subject><subject>Hydroxyurea - chemistry</subject><subject>Inorganic chemistry and origins of life</subject><subject>Iron - chemistry</subject><subject>Iron(III) complexes</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Oxidation-Reduction</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Preparations and properties</topic><topic>Voltammetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NIGOVIC, Biljana</creatorcontrib><creatorcontrib>KUJUNDZIC, Nikola</creatorcontrib><creatorcontrib>SANKOVIC, Kresimir</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NIGOVIC, Biljana</au><au>KUJUNDZIC, Nikola</au><au>SANKOVIC, Kresimir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electron transfer in N-hydroxyurea complexes with iron(III)</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2005</date><risdate>2005</risdate><volume>40</volume><issue>1</issue><spage>51</spage><epage>55</epage><pages>51-55</pages><issn>0223-5234</issn><eissn>1768-3254</eissn><coden>EJMCA5</coden><abstract>Redox behaviour of the iron(III) complex with the antitumour drug hydroxyurea was studied by cyclic voltammetry. The complex underwent a one-electron reduction, followed by an irreversible chemical reaction (EC mechanism) in which a ligand was released. In addition, it was found that the hydroxyurea gave up an electron to iron(III) in solution. Differential-pulse voltammetry revealed an increase in the concentration of the generated iron(II) species. Electron paramagnetic resonance (EPR) spectroscopy studies of the oxidative degradation of hydroxyurea confirmed formation of the radical species H
2N–CO–NHO
.. Electrochemical data for iron(III) complexes of hydroxyurea and its structural analogue 3-ethylhydroxyurea, which also exhibits antitumour activity, show the same mechanism involved in the electron transfer. The observed redox properties indicate that hydroxyurea may interfere with electron transfer processes in biological systems after binding to iron-containing ribonucleotide reductase.</abstract><cop>Oxford</cop><pub>Elsevier Masson SAS</pub><pmid>15642408</pmid><doi>10.1016/j.ejmech.2004.09.012</doi><tpages>5</tpages></addata></record> |
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subjects | Antineoplastic Agents - chemistry Biological and medical sciences Chemistry Coordination compounds Electrochemistry Electron Spin Resonance Spectroscopy Electron transfer EPR Exact sciences and technology Hydroxyurea Hydroxyurea - chemistry Inorganic chemistry and origins of life Iron - chemistry Iron(III) complexes Medical sciences Miscellaneous Oxidation-Reduction Pharmacology. Drug treatments Preparations and properties Voltammetry |
title | Electron transfer in N-hydroxyurea complexes with iron(III) |
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