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Pregled bibliografske jedinice broj: 458780

Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins


Kos, Ivan; Rebouças, J.S.; DeFreitas-Silva, G.; Salvemini, D.; Vujasković, Željko; Dewhirst, M.W.; Spasojević, Ivan; Batinić-Haberle, Ines
Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins // Free radical biology & medicine, 47 (2009), 1; 72-78 doi:10.1016/j.freeradbiomed.2009.04.002 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 458780 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins

Autori
Kos, Ivan ; Rebouças, J.S. ; DeFreitas-Silva, G. ; Salvemini, D. ; Vujasković, Željko ; Dewhirst, M.W. ; Spasojević, Ivan ; Batinić-Haberle, Ines

Izvornik
Free radical biology & medicine (0891-5849) 47 (2009), 1; 72-78

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

Ključne riječi
Mn(III) N-alkylpyridylporphyrins ; SOD mimics ; lipophilicity

Sažetak
Mn(III) N-alkylpyridylporphyrins are among the most potent known SOD mimics and catalytic peroxynitrite scavengers and modulators of redox-based cellular transcriptional activity. In addition to their intrinsic antioxidant capacity, bioavailability plays a major role in their in vivo efficacy. Although of identical antioxidant capacity, lipophilic MnTnHex-2-PyP is up to 120-fold more efficient in reducing oxidative stress injuries than hydrophilic MnTE-2-PyP. Owing to limitations of an analytical nature, porphyrin lipophilicity has been often estimated by the thin-layer chromatographic R(f) parameter, instead of the standard n-octanol/water partition coefficient, P(OW). Herein we used a new methodological approach to finally describe the MnP lipophilicity, using the conventional log P(OW) means, for a series of biologically active ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins. Three new porphyrins (MnTnBu-3-PyP, MnTnHex-3-PyP, and MnTnHep-2-PyP) were synthesized to strengthen the conclusions. The log P(OW) was linearly related to R(f) and to the number of carbons in the alkyl chain (n(C)) for both isomer series, the meta isomers being 10-fold more lipophilic than the analogous ortho porphyrins. Increasing the length of the alkyl chain by one carbon atom increases the log P(OW) value approximately 1 log unit with both isomers. Dramatic approximately 4 and approximately 5 orders of magnitude increases in the lipophilicity of the ortho isomers, by extending the pyridyl alkyl chains from two (MnTE-2-PyP, log P(OW)=-6.89) to six (MnTnHex-2-PyP, log P(OW)=-2.76) and eight carbon atoms (MnTnOct-2-PyP, log P(OW)=-1.24), parallels the increased efficacy in several oxidative-stress injury models, particularly those of the central nervous system, in which transport across the blood-brain barrier is critical. Although meta isomers are only slightly less potent SOD mimics and antioxidants than their ortho analogues, their higher lipophilicity and smaller bulkiness may lead to a higher cellular uptake and overall similar effectiveness in vivo.

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Biologija, Farmacija



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 Ivan Kos (autor)

Avatar Url Ines Batinić-Haberle (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com

Citiraj ovu publikaciju:

Kos, Ivan; Rebouças, J.S.; DeFreitas-Silva, G.; Salvemini, D.; Vujasković, Željko; Dewhirst, M.W.; Spasojević, Ivan; Batinić-Haberle, Ines
Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins // Free radical biology & medicine, 47 (2009), 1; 72-78 doi:10.1016/j.freeradbiomed.2009.04.002 (međunarodna recenzija, članak, znanstveni)
Kos, I., Rebouças, J., DeFreitas-Silva, G., Salvemini, D., Vujasković, Ž., Dewhirst, M., Spasojević, I. & Batinić-Haberle, I. (2009) Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins. Free radical biology & medicine, 47 (1), 72-78 doi:10.1016/j.freeradbiomed.2009.04.002.
@article{article, author = {Kos, Ivan and Rebou\c{c}as, J.S. and DeFreitas-Silva, G. and Salvemini, D. and Vujaskovi\'{c}, \v{Z}eljko and Dewhirst, M.W. and Spasojevi\'{c}, Ivan and Batini\'{c}-Haberle, Ines}, year = {2009}, pages = {72-78}, DOI = {10.1016/j.freeradbiomed.2009.04.002}, keywords = {Mn(III) N-alkylpyridylporphyrins, SOD mimics, lipophilicity}, journal = {Free radical biology and medicine}, doi = {10.1016/j.freeradbiomed.2009.04.002}, volume = {47}, number = {1}, issn = {0891-5849}, title = {Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins}, keyword = {Mn(III) N-alkylpyridylporphyrins, SOD mimics, lipophilicity} }
@article{article, author = {Kos, Ivan and Rebou\c{c}as, J.S. and DeFreitas-Silva, G. and Salvemini, D. and Vujaskovi\'{c}, \v{Z}eljko and Dewhirst, M.W. and Spasojevi\'{c}, Ivan and Batini\'{c}-Haberle, Ines}, year = {2009}, pages = {72-78}, DOI = {10.1016/j.freeradbiomed.2009.04.002}, keywords = {Mn(III) N-alkylpyridylporphyrins, SOD mimics, lipophilicity}, journal = {Free radical biology and medicine}, doi = {10.1016/j.freeradbiomed.2009.04.002}, volume = {47}, number = {1}, issn = {0891-5849}, title = {Lipophilicity of potent porphyrin-based antioxidants : comparison of ortho and meta isomers of Mn(III) N-alkylpyridylporphyrins}, keyword = {Mn(III) N-alkylpyridylporphyrins, SOD mimics, lipophilicity} }

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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