In vitro comparison of the acetylcholinesterase inhibition caused by V- and A-series nerve agents' surrogates
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
37595776
DOI
10.1016/j.cbi.2023.110678
PII: S0009-2797(23)00345-9
Knihovny.cz E-zdroje
- Klíčová slova
- Acetylcholinesterase, Inhibitors, Organophosphorus surrogates, Reactivation,
- MeSH
- acetylcholinesterasa * MeSH
- nebezpečné látky MeSH
- nervová bojová látka * toxicita MeSH
- organofosforové sloučeniny toxicita MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- acetylcholinesterasa * MeSH
- nebezpečné látky MeSH
- nervová bojová látka * MeSH
- organofosforové sloučeniny MeSH
Nerve agents (NA) pose as a great risk in the modern world. NA from the V-series, such as VX, are currently recognized as the most toxic among those compounds. However, the emergence of new classes of toxicants recently included in the Chemical Weapons Convention (CWC), such as the A-series NA, a class of organophosphorus compounds related to phosphoramidates, pose a new source of concern due to the lack of information. In order advance in the investigation on the toxicity of such toxic chemicals, we performed in vitro studies to compare representatives of the V- and A-series using affordable surrogates. Results suggest a similar inhibition potency between both agents.
Institute of Chemical Biological Radiological and Nuclear Defense Rio de Janeiro Brazil
Laboratory of Molecular Modeling Applied to Chemical and Biological Defense Rio de Janeiro Brazil
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