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Statements

Subject Item
n2:RIV%2F60162694%3AG38__%2F03%3A00000903%21RIV%2F2005%2FMO0%2FG38005%2FN
rdf:type
skos:Concept n12:Vysledek
dcterms:description
In this article, we have followed up the relationship between the ability to reactivate acetylcholinesterase inhibited by organophosphorus compounds and the length of linking chainbetween two 4-hydroxyiminomethylpyridinium rings of acetylcholinesterase reactivators. aw-bis(4-hydroxyiminomethylpyridinium) alkanes have been used as the tested acetylcholinesterase reactivators. These oximes differ in the number of methylene groups on the connecting chain. A three or four membered linking chain seems to bethe ideal length for the satisfactory reactivation potency with the exception of reactivators of cyclosarin-inhibited acetylcholinesterase. In this case, the most efficacious acetylcholinesterase reactivator has one methylene group on the connecting chain Reaktivace aktivity acetylcholinesterázy inhibované organofosfáty pomocí a,w-bis-(4-hydroxyiminomethylpyridinium)alkanes in vitro In this article, we have followed up the relationship between the ability to reactivate acetylcholinesterase inhibited by organophosphorus compounds and the length of linking chainbetween two 4-hydroxyiminomethylpyridinium rings of acetylcholinesterase reactivators. aw-bis(4-hydroxyiminomethylpyridinium) alkanes have been used as the tested acetylcholinesterase reactivators. These oximes differ in the number of methylene groups on the connecting chain. A three or four membered linking chain seems to bethe ideal length for the satisfactory reactivation potency with the exception of reactivators of cyclosarin-inhibited acetylcholinesterase. In this case, the most efficacious acetylcholinesterase reactivator has one methylene group on the connecting chain
dcterms:title
Reaktivace aktivity acetylcholinesterázy inhibované organofosfáty pomocí a,w-bis-(4-hydroxyiminomethylpyridinium)alkanes in vitro Reactivation of organophosphate inhibited acetylcholinesterase activity by a,w-bis-(4-hydroxyiminomethylpyridinium) alcanes in vitro Reactivation of organophosphate inhibited acetylcholinesterase activity by a,w-bis-(4-hydroxyiminomethylpyridinium) alcanes in vitro
skos:prefLabel
Reaktivace aktivity acetylcholinesterázy inhibované organofosfáty pomocí a,w-bis-(4-hydroxyiminomethylpyridinium)alkanes in vitro Reactivation of organophosphate inhibited acetylcholinesterase activity by a,w-bis-(4-hydroxyiminomethylpyridinium) alcanes in vitro Reactivation of organophosphate inhibited acetylcholinesterase activity by a,w-bis-(4-hydroxyiminomethylpyridinium) alcanes in vitro
skos:notation
RIV/60162694:G38__/03:00000903!RIV/2005/MO0/G38005/N
n5:strany
207-211
n5:aktivita
n18:P
n5:aktivity
P(OBVLAJEP20032), P(ON03021100001)
n5:cisloPeriodika
4
n5:dodaniDat
n6:2005
n5:domaciTvurceVysledku
n14:3691314 n14:6306888 n14:5211336
n5:druhVysledku
n17:J
n5:duvernostUdaju
n16:S
n5:entitaPredkladatele
n8:predkladatel
n5:idSjednocenehoVysledku
624635
n5:idVysledku
RIV/60162694:G38__/03:00000903
n5:jazykVysledku
n10:eng
n5:klicovaSlova
acetylcholinesterase;organophosporus compounds;tabun;sarin;cyclosarin;VX
n5:klicoveSlovo
n9:tabun n9:VX n9:acetylcholinesterase n9:cyclosarin n9:sarin n9:organophosporus%20compounds
n5:kodStatuVydavatele
CZ - Česká republika
n5:kontrolniKodProRIV
[46DDF41B2772]
n5:nazevZdroje
Journal of Applied Biomedicine
n5:obor
n7:FP
n5:pocetDomacichTvurcuVysledku
3
n5:pocetTvurcuVysledku
3
n5:projekt
n13:ON03021100001 n13:OBVLAJEP20032
n5:rokUplatneniVysledku
n6:2003
n5:svazekPeriodika
1
n5:tvurceVysledku
Patočka, Jiří Kuča, Kamil Cabal, Jiří
s:issn
1214-021X
s:numberOfPages
5
n15:organizacniJednotka
G38