In vitro reactivation of tabun-inhibited acetylcholinesterase using new oximes--K027, K005, K033 and K048
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15141981
Knihovny.cz E-zdroje
- MeSH
- cholinesterasové inhibitory toxicita MeSH
- krysa rodu Rattus MeSH
- mozek enzymologie MeSH
- organofosfáty toxicita MeSH
- oximy chemická syntéza farmakologie toxicita MeSH
- pyridinové sloučeniny chemická syntéza farmakologie toxicita MeSH
- reaktivátory cholinesterázy chemická syntéza farmakologie MeSH
- techniky in vitro MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1-(4-hydroxyiminomethylpyridinium)-3-(carbamoylpyridinium) propane dibromide MeSH Prohlížeč
- 1,3-bis(2-hydroxyiminomethylpyridinium)propane MeSH Prohlížeč
- 1,4-bis(2-hydroxyiminomethylpyridinium)butane MeSH Prohlížeč
- cholinesterasové inhibitory MeSH
- organofosfáty MeSH
- oximy MeSH
- pyridinové sloučeniny MeSH
- reaktivátory cholinesterázy MeSH
- tabun MeSH Prohlížeč
Four new AChE oximes for reactivation of acetylcholinesterase inhibited with tabun - K027 [1-(4-hydroxyiminomethylpyridinium)-3-(4-carbamoylpyridinium) propane dibromide], K005 [1,3-bis(2-hydroxyiminomethylpyridinium) propane dibromide], K033 [1,4-bis(2-hydroxyiminomethylpyridinium) butane dibromide] and K048 [1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium) butane dibromide] were prepared. Their efficacies to reactivate tabun-inhibited acetylcholinesterase were studied and compared with the currently used acetylcholinesterase reactivators (pralidoxime, obidoxime and HI-6). Reactivator K048 seems to be promising reactivator of tabun-inhibited AChE. Its reactivation potency is significantly higher than the efficacy of HI-6 and pralidoxime, and comparable with the potency of the obidoxime at human relevant doses.
Experimental and Established Oximes as Pretreatment before Acute Exposure to Azinphos-Methyl
Combined Pre- and Posttreatment of Paraoxon Exposure
Reactivation of sarin-inhibited pig brain acetylcholinesterase using oxime antidotes