Pregled bibliografske jedinice broj: 633287
Efficiency of novel heterocyclic oximes in reactivation of paraoxon-inhibited cholinesterases
Efficiency of novel heterocyclic oximes in reactivation of paraoxon-inhibited cholinesterases // 14th Medical Chemical Defence Conference 2013: Translation of experimental research for improved treatment of chemical warfare agent poisoning
München, 2013. str. 61-61 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 633287 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Efficiency of novel heterocyclic oximes in
reactivation of paraoxon-inhibited cholinesterases
Autori
Morasi Piperčić, Sara ; Makarić , Sandro ; Baumann, Krešimir ; Primožič , Ines ; Tomić- Pisarović , Srđanka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
14th Medical Chemical Defence Conference 2013: Translation of experimental research for improved treatment of chemical warfare agent poisoning
/ - München, 2013, 61-61
Skup
14th Medical Chemical Defence Conference 2013
Mjesto i datum
München, Njemačka, 23.04.2013. - 25.04.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
oxime ; cholinesterase ; antidote
Sažetak
Toxic cholinesterase inhibiting compounds like organophosphates (OP) and carbamates are intensively used and produced troughout the world and continue to be responsible for poisoning and deaths.Chemical warfare agents are of outmost concern due to their possible use in wars and terrorist attacks. Since there is still no single, broad-spectrum compound suitable for the antidotal treatment of poisoning with all OP agents a series of novel aliphatic and aromatic quaternary salts of N- alkyl/aryl imidazol- and benzimidazole-2- aldoximes have been prepared as potential reactivators of inhibited butyrylcholinesterase. N-alkylations of commercially available heterocyclic azoles resulted in their N-alkyl/aryl derivatives. N- alkyl/aryl imidazoles and benzimidazoles were converted to the appropriate 2-carbaldehydes by using modified Ivesen-Lund method and then to 2-aldoximes. Reaction of the oximes with the alkyl/aryl halogenides resulted in a desired quaternary salts. Structures of prepared compounds were deduced from IR, one- and twodimensional NMR and MS spectra. Ellmans method and acetylthiocholine as substrate will be used to test inhibitory properties of prepared compounds and their reactivation efficiency of Paraoxon™ inhibited HuAChE and HuBChE, as well as lyophilised EqBChE and RSBChE. Structural characteristics of an efficient oxime reactivator will be discussed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-119-1191344-3121 - Sinteze i enzimske transformacije biološki aktivnih spojeva (Tomić-Pisarović, Srđanka, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Sara Morasi Pipercic (autor)
Krešimir Baumann (autor)
Srđanka Tomić-Pisarović (autor)
Ines Primožič (autor)