Influence of the distance between quaternary nitrogen and oxime group on the reactivation ability of oximes - antidotes against nerve agents
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F13%3A43874790" target="_blank" >RIV/60162694:G44__/13:43874790 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.stmconnect.com/sites/default/files/41-43%20%20JEIT-D-12-00014.pdf" target="_blank" >http://www.stmconnect.com/sites/default/files/41-43%20%20JEIT-D-12-00014.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.7178/jeit.16" target="_blank" >10.7178/jeit.16</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Influence of the distance between quaternary nitrogen and oxime group on the reactivation ability of oximes - antidotes against nerve agents
Popis výsledku v původním jazyce
Cholinesterase reactivators are a group of drugs originally developed as antidotes for treatment of nerve agent intoxications. Although there are five commercially available members of this group, none is considered to be a universal solution for treatment of intoxication caused by all nerve agents. Due to this, novel drug candidates are searched. To find the most promising antidotes, structure activity studies are conducted. In this contribution, distance between quaternary nitrogen and aldoxime (called oxime) group responsible for the reactivation process is discussed. For this purpose, three structurally different oxime reactivators were tested for their potency to reactivate tabun, sarin, cyclosarin and VX agent-inhibited acetylcholinesterase (AC hE; EC 3.1.1.7). As resulted, only "standard" oxime reactivators with oxime group connected to the heteroaromatic ring could be considered as promising AC hE reactivators. Those with oxime group on other aromatic ring or those with quatern
Název v anglickém jazyce
Influence of the distance between quaternary nitrogen and oxime group on the reactivation ability of oximes - antidotes against nerve agents
Popis výsledku anglicky
Cholinesterase reactivators are a group of drugs originally developed as antidotes for treatment of nerve agent intoxications. Although there are five commercially available members of this group, none is considered to be a universal solution for treatment of intoxication caused by all nerve agents. Due to this, novel drug candidates are searched. To find the most promising antidotes, structure activity studies are conducted. In this contribution, distance between quaternary nitrogen and aldoxime (called oxime) group responsible for the reactivation process is discussed. For this purpose, three structurally different oxime reactivators were tested for their potency to reactivate tabun, sarin, cyclosarin and VX agent-inhibited acetylcholinesterase (AC hE; EC 3.1.1.7). As resulted, only "standard" oxime reactivators with oxime group connected to the heteroaromatic ring could be considered as promising AC hE reactivators. Those with oxime group on other aromatic ring or those with quatern
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FR - Farmakologie a lékárnická chemie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/NT12062" target="_blank" >NT12062: Příprava a hodnocení účinnosti nových terapeutik proti otravám pesticidy</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2013
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Environmental Immunology and Toxicology
ISSN
2225-1219
e-ISSN
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Svazek periodika
1
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
3
Strana od-do
41-43
Kód UT WoS článku
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EID výsledku v databázi Scopus
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