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Statements

Subject Item
n2:RIV%2F60162694%3AG38__%2F04%3A00001076%21RIV%2F2005%2FMO0%2FG38005%2FN
rdf:type
skos:Concept n17:Vysledek
dcterms:description
Syntéza biskvartérních symetrickéch - c,d-Bis(2-Hydroxyiminomethylpyridinium)alkán dibromidů a jejich reaktivace cyklosarinam-inhibované acetylcholinesterázy Preparations of the symmetric bisquaternary oximes - 1,4-bis(2-hydroxyiminomethypyridinium)butane dibromide and 1,3-bis(2-hydroxyiminomethypyridinium)propane dibromide, and their abilities to reactivate cyclosarin-inhibited acetylcholinesterase are described. Common reactivator (pralidoxime) was used as a standard for comparison of the reactivation efficacy. The first oxime seems to be very good reactivator of cyclosarin-inhibited acetylcholinesterase. Preparations of the symmetric bisquaternary oximes - 1,4-bis(2-hydroxyiminomethypyridinium)butane dibromide and 1,3-bis(2-hydroxyiminomethypyridinium)propane dibromide, and their abilities to reactivate cyclosarin-inhibited acetylcholinesterase are described. Common reactivator (pralidoxime) was used as a standard for comparison of the reactivation efficacy. The first oxime seems to be very good reactivator of cyclosarin-inhibited acetylcholinesterase.
dcterms:title
Synthesis of bisquaternary symmetric - c,d-bis(2-hydroxyiminomethylpyridinium)alkane dibromides and their reactivation of cyclosarin-inhibited acetylcholinesterase Synthesis of bisquaternary symmetric - c,d-bis(2-hydroxyiminomethylpyridinium)alkane dibromides and their reactivation of cyclosarin-inhibited acetylcholinesterase Syntéza biskvartérních symetrickéch - c,d-Bis(2-Hydroxyiminomethylpyridinium)alkán dibromidů a jejich reaktivace cyklosarinam-inhibované acetylcholinesterázy
skos:prefLabel
Syntéza biskvartérních symetrickéch - c,d-Bis(2-Hydroxyiminomethylpyridinium)alkán dibromidů a jejich reaktivace cyklosarinam-inhibované acetylcholinesterázy Synthesis of bisquaternary symmetric - c,d-bis(2-hydroxyiminomethylpyridinium)alkane dibromides and their reactivation of cyclosarin-inhibited acetylcholinesterase Synthesis of bisquaternary symmetric - c,d-bis(2-hydroxyiminomethylpyridinium)alkane dibromides and their reactivation of cyclosarin-inhibited acetylcholinesterase
skos:notation
RIV/60162694:G38__/04:00001076!RIV/2005/MO0/G38005/N
n3:strany
84-86
n3:aktivita
n18:P
n3:aktivity
P(ONVLAJEP20031)
n3:cisloPeriodika
1
n3:dodaniDat
n10:2005
n3:domaciTvurceVysledku
n8:5211336 n8:3691314 n8:2182262 n8:6306888
n3:druhVysledku
n5:J
n3:duvernostUdaju
n14:S
n3:entitaPredkladatele
n16:predkladatel
n3:idSjednocenehoVysledku
589341
n3:idVysledku
RIV/60162694:G38__/04:00001076
n3:jazykVysledku
n4:eng
n3:klicovaSlova
oximes;reactivation;acetylcholinesterase;cyclosarin;in vitro
n3:klicoveSlovo
n11:reactivation n11:oximes n11:in%20vitro n11:cyclosarin n11:acetylcholinesterase
n3:kodStatuVydavatele
AE - Stát Spojené arabské emiráty
n3:kontrolniKodProRIV
[508CDF57715B]
n3:nazevZdroje
Letters in Organic Chemistry
n3:obor
n9:FP
n3:pocetDomacichTvurcuVysledku
4
n3:pocetTvurcuVysledku
4
n3:projekt
n15:ONVLAJEP20031
n3:rokUplatneniVysledku
n10:2004
n3:svazekPeriodika
1
n3:tvurceVysledku
Kuča, Kamil Kassa, Jiří Patočka, Jiří Cabal, Jiří
s:issn
1570-1786
s:numberOfPages
3
n12:organizacniJednotka
G38