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Pregled bibliografske jedinice broj: 593970

Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate


Kalmár, József; Biri, Bernadett; Lente, Gábor; Bányai, István; Budimir, Ana; Biruš, Mladen; Batinić-Haberle, Ines; Fábián, István
Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate // Dalton transactions, 41 (2012), 38; 11875-11884 doi:10.1039/C2DT31200J (međunarodna recenzija, članak, znanstveni)


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Naslov
Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate

Autori
Kalmár, József ; Biri, Bernadett ; Lente, Gábor ; Bányai, István ; Budimir, Ana ; Biruš, Mladen ; Batinić-Haberle, Ines ; Fábián, István

Izvornik
Dalton transactions (1477-9226) 41 (2012), 38; 11875-11884

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
hydroxyurea ; Mn porphyrin ; kinetics ; mechanism

Sažetak
The in vitro autoxidation of N-hydroxyurea (HU) is catalyzed by MnIIITTEG-2-PyP5+, a synthetic water soluble Mn(III) porphyrin which is also a potent mimic of the enzyme superoxide dismutase. The detailed mechanism of the reaction is deduced from kinetic studies under basic conditions mostly based on data measured at pH = 11.7 but also including some pH-dependent observations in the pH range 9–13. The major intermediates were identified by UV-vis spectroscopy and electrospray ionization mass spectrometry. The reaction starts with a fast axial coordination of HU to the metal center of MnIIITTEG-2-PyP5+, which is followed by a ligand-to-metal electron transfer to get MnIITTEG-2-PyP4+ and the free radical derived from HU (HU˙). Nitric oxide (NO) and nitroxyl (HNO) are minor intermediates. The major pathway for the formation of the most significant intermediate, the {; ; ; ; MnNO}; ; ; ; complex of MnIITTEG-2-PyP4+, is the reaction of MnIITTEG-2-PyP4+ with NO. We have confirmed that the autoxidation of the intermediates opens alternative reaction channels, and the process finally yields NO2− and the initial MnIIITTEG-2-PyP5+. The photochemical release of NO from the {; ; ; ; MnNO}; ; ; ; intermediate was also studied. Kinetic simulations were performed to validate the deduced rate constants. The investigated reaction has medical implications: the accelerated production of NO and HNO from HU may be utilized for therapeutic purposes.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
006-0061247-0009 - Kinetika i mehanizam katalitičkog antioksidacijskog djelovanja Mn-porfirina (Budimir, Ana, MZOS ) ( CroRIS)

Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb

Profili:

Avatar Url Mladen Biruš (autor)

Avatar Url Ana Budimir (autor)

Avatar Url Ines Batinić-Haberle (autor)

Poveznice na cjeloviti tekst rada:

doi pubs.rsc.org

Citiraj ovu publikaciju:

Kalmár, József; Biri, Bernadett; Lente, Gábor; Bányai, István; Budimir, Ana; Biruš, Mladen; Batinić-Haberle, Ines; Fábián, István
Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate // Dalton transactions, 41 (2012), 38; 11875-11884 doi:10.1039/C2DT31200J (međunarodna recenzija, članak, znanstveni)
Kalmár, J., Biri, B., Lente, G., Bányai, I., Budimir, A., Biruš, M., Batinić-Haberle, I. & Fábián, I. (2012) Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate. Dalton transactions, 41 (38), 11875-11884 doi:10.1039/C2DT31200J.
@article{article, author = {Kalm\'{a}r, J\'{o}zsef and Biri, Bernadett and Lente, G\'{a}bor and B\'{a}nyai, Istv\'{a}n and Budimir, Ana and Biru\v{s}, Mladen and Batini\'{c}-Haberle, Ines and F\'{a}bi\'{a}n, Istv\'{a}n}, year = {2012}, pages = {11875-11884}, DOI = {10.1039/C2DT31200J}, keywords = {hydroxyurea, Mn porphyrin, kinetics, mechanism}, journal = {Dalton transactions}, doi = {10.1039/C2DT31200J}, volume = {41}, number = {38}, issn = {1477-9226}, title = {Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate}, keyword = {hydroxyurea, Mn porphyrin, kinetics, mechanism} }
@article{article, author = {Kalm\'{a}r, J\'{o}zsef and Biri, Bernadett and Lente, G\'{a}bor and B\'{a}nyai, Istv\'{a}n and Budimir, Ana and Biru\v{s}, Mladen and Batini\'{c}-Haberle, Ines and F\'{a}bi\'{a}n, Istv\'{a}n}, year = {2012}, pages = {11875-11884}, DOI = {10.1039/C2DT31200J}, keywords = {hydroxyurea, Mn porphyrin, kinetics, mechanism}, journal = {Dalton transactions}, doi = {10.1039/C2DT31200J}, volume = {41}, number = {38}, issn = {1477-9226}, title = {Detailed mechanism of the autoxidation of N-hydroxyurea catalyzed by a superoxide dismutase mimic Mn(III) porphyrin: formation of the nitrosylated Mn(II) porphyrin as an intermediate}, keyword = {hydroxyurea, Mn porphyrin, kinetics, mechanism} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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