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rdf:type
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Description
| - Reactivators of acetylcholinesterase (AChE; EC 3.1.1.7) are compounds, which are able to treat intoxication with organophosphorus compounds, especially with pesticides or nerve agents. Owing to the fact that there exist no universal %22broad-spectrum%22 reactivator of oranophosphates-inhibited AChE, many laboratories from the world synthesize new AChE reactivators. In our work, there were synthesized five new and three already known quaternary monopyridinium oximes as potential reactivators of AChE inhibited by nerve agents. Potencies to cleave p-nitrophenyl acetate (PNPA), which is commonly used as model substrate of the nerve agents, were measured. Their cleaving potencies were compared with 4-PAM (4-hydroxyiminomethyl-1-methylpyridinium iodide), which is derived from the structure of the currently used AChE-reactivator 2-PAM (2-hydroxyiminomethyl-1-methylpyridinium iodide). Three newly synthesized oximes achieved similar nuclephilicity at the similar pKa according to 4-PAM, what is very promi
- Reactivators of acetylcholinesterase (AChE; EC 3.1.1.7) are compounds, which are able to treat intoxication with organophosphorus compounds, especially with pesticides or nerve agents. Owing to the fact that there exist no universal %22broad-spectrum%22 reactivator of oranophosphates-inhibited AChE, many laboratories from the world synthesize new AChE reactivators. In our work, there were synthesized five new and three already known quaternary monopyridinium oximes as potential reactivators of AChE inhibited by nerve agents. Potencies to cleave p-nitrophenyl acetate (PNPA), which is commonly used as model substrate of the nerve agents, were measured. Their cleaving potencies were compared with 4-PAM (4-hydroxyiminomethyl-1-methylpyridinium iodide), which is derived from the structure of the currently used AChE-reactivator 2-PAM (2-hydroxyiminomethyl-1-methylpyridinium iodide). Three newly synthesized oximes achieved similar nuclephilicity at the similar pKa according to 4-PAM, what is very promi (en)
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Title
| - New group of monoquaternary reactivators of the acetylcholinesterase inhibited by nerve agents
- New group of monoquaternary reactivators of the acetylcholinesterase inhibited by nerve agents (en)
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skos:prefLabel
| - New group of monoquaternary reactivators of the acetylcholinesterase inhibited by nerve agents
- New group of monoquaternary reactivators of the acetylcholinesterase inhibited by nerve agents (en)
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skos:notation
| - RIV/60162694:G44__/05:00001349!RIV10-MO0-G44_____
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/60162694:G44__/05:00001349
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - Acetylcholinesterase; Reactivator; PNPA; Reactivation; Nerve agents; Inhibition (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - GB - Spojené království Velké Británie a Severního Irska
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Journal of Enzyme Inhibition and Medicinal Chemistry
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Cabal, Jiří
- Kuča, Kamil
- Liška, F.
- Kohout, M.
- Pícha, J.
- Kivala, M.
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http://linked.open...ain/vavai/riv/wos
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issn
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number of pages
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http://localhost/t...ganizacniJednotka
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