Pregled bibliografske jedinice broj: 447095
Synthesis and evaluation of novel analogues of vitamin B6 as reactivators of tabun and paraoxon inhibited acetylcholinesterase
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)
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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
Profili:
Valentina Bušić
(autor)
Maja Katalinić
(autor)
Dajana Gašo-Sokač
(autor)
Zrinka Kovarik
(autor)
Spomenka Kovač
(autor)
Citiraj ovu publikaciju:
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