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Pregled bibliografske jedinice broj: 447095

Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase


Gašo-Sokač, Dajana; Katalinić, Maja; Kovarik, Zrinka; Bušić, Valentina; Kovač, Spomenka
Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase // Chemico-biological interactions, 187 (2010), 1/3; 234-237 doi:10.1016/j.cbi.2010.02.004 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 447095 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase

Autori
Gašo-Sokač, Dajana ; Katalinić, Maja ; Kovarik, Zrinka ; Bušić, Valentina ; Kovač, Spomenka

Izvornik
Chemico-biological interactions (0009-2797) 187 (2010), 1/3; 234-237

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

Ključne riječi
acetylcholinesterase; tabun; paraoxon; pyridoxal oxime; reactivation

Sažetak
A series of novel pyridinium oximes was prepared by reactions of quaternization of pyridoxal oxime with substituted phenacyl bromides in acetone at room temperature. The structures of compounds were determined according to the data obtained by IR spectroscopy, mass spectrometry, 1H and 13C nuclear magnetic resonance spectroscopy as well as by elemental analysis. We tested pyridoxal oxime (1) and five prepared oximes in 1 mM concentration as reactivators of human erythrocytes acetylcholinesterase (AChE) inhibited by organophosphorus compounds tabun and paraoxon: 1-phenacyl-3-hydroxy-4-hydroxyiminomethyl-5-hydroxymethyl-2-methylpyridinium bromide (2), 1-(4′-chlorophenacyl)-3-hydroxy-4-hydroxyiminomethyl-5-hydroxymethyl-2-methylpyridinium bromide (3), 1-(4′-fluorophenacyl)-3-hydroxy-4-hydroxyiminomethyl-5-hydroxymethyl-2-methylpyridinium bromide (4), 3-hydroxy-4-hydroxyiminomethyl-5-hydroxymethyl-2-methyl-1-(4′-methylphenacyl)pyridinium bromide (5), 3-hydroxy-4-hydroxyiminomethyl-5-hydroxymethyl-2-methyl-1-(4′-methoxyphenacyl)pyridinium bromide (6). However, tested oximes were not efficient in reactivation of either tabun or paraoxon inhibited AChE. The maximum restored enzyme activity in 24 h was below 25%. Therefore, this class of compounds cannot be considered as potential improvement in a search for new and more efficient antidotes against OP poisoning.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

Napomena
Rad je prezentiran na skupu 10th International Meeting on Cholinesterases ; Elsa Reiner, Jean Massoulié, Terrone Rosenberry, Peter Eyer, Gabi Amitai, Zoran Radić, Zrinka Kovarik (ur.).



POVEZANOST RADA


Projekti:
022-0222148-2889 - Interakcije organofosfata, karbamata i određenih liganada s esterazama (Kovarik, Zrinka, MZOS ) ( CroRIS)
291-0580000-0169 - Kemijski senzori za primjenu u biomedicini, hrani i zaštiti okoliša (Sak-Bosnar, Milan, MZOS ) ( CroRIS)

Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb,
Prehrambeno-tehnološki fakultet, Osijek,
Sveučilište u Osijeku - Odjel za kemiju

Citiraj ovu publikaciju:

Gašo-Sokač, Dajana; Katalinić, Maja; Kovarik, Zrinka; Bušić, Valentina; Kovač, Spomenka
Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase // Chemico-biological interactions, 187 (2010), 1/3; 234-237 doi:10.1016/j.cbi.2010.02.004 (međunarodna recenzija, članak, znanstveni)
Gašo-Sokač, D., Katalinić, M., Kovarik, Z., Bušić, V. & Kovač, S. (2010) Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase. Chemico-biological interactions, 187 (1/3), 234-237 doi:10.1016/j.cbi.2010.02.004.
@article{article, author = {Ga\v{s}o-Soka\v{c}, Dajana and Katalini\'{c}, Maja and Kovarik, Zrinka and Bu\v{s}i\'{c}, Valentina and Kova\v{c}, Spomenka}, year = {2010}, pages = {234-237}, DOI = {10.1016/j.cbi.2010.02.004}, keywords = {acetylcholinesterase, tabun, paraoxon, pyridoxal oxime, reactivation}, journal = {Chemico-biological interactions}, doi = {10.1016/j.cbi.2010.02.004}, volume = {187}, number = {1/3}, issn = {0009-2797}, title = {Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase}, keyword = {acetylcholinesterase, tabun, paraoxon, pyridoxal oxime, reactivation} }
@article{article, author = {Ga\v{s}o-Soka\v{c}, Dajana and Katalini\'{c}, Maja and Kovarik, Zrinka and Bu\v{s}i\'{c}, Valentina and Kova\v{c}, Spomenka}, year = {2010}, pages = {234-237}, DOI = {10.1016/j.cbi.2010.02.004}, keywords = {acetylcholinesterase, tabun, paraoxon, pyridoxal oxime, reactivation}, journal = {Chemico-biological interactions}, doi = {10.1016/j.cbi.2010.02.004}, volume = {187}, number = {1/3}, issn = {0009-2797}, title = {Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase}, keyword = {acetylcholinesterase, tabun, paraoxon, pyridoxal oxime, reactivation} }

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


Citati:





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