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Pregled bibliografske jedinice broj: 633287

Efficiency of novel heterocyclic oximes in reactivation of paraoxon-inhibited cholinesterases


Morasi Piperčić, Sara; Makarić , Sandro; Baumann, Krešimir; Primožič , Ines; Tomić-Pisarović , Srđanka
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, Njemačka, 2013. str. 61-61 (poster, međunarodna recenzija, sažetak, znanstveni)


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, Njemačka, 2013, 61-61

Skup
14th Medical Chemical Defence Conference 2013

Mjesto i datum
München, Njemačka, 23.-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


Projekt / tema
119-1191344-3121 - Sinteze i enzimske transformacije biološki aktivnih spojeva (Srđanka Tomić-Pisarović, )

Ustanove
Prirodoslovno-matematički fakultet, Zagreb