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  2. Soman - Wikipedia

    en.wikipedia.org/wiki/Soman

    No metabolic toxification reactions are known for soman. Soman can be hydrolyzed by a so-called A-esterase, more specific a diisopropylfluorophosphatase. This esterase, also called somanase, reacts with the anhydride bond between phosphorus and fluorine and accounts for the hydrolysis of the fluoride.

  3. Organophosphorus acid anhydrolase - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_acid_an...

    OPAA’s susbstrate-specificity to organophosphorus-containing compounds, especially fluoride-containing G-type nerve agents such as sarin, cyclosarin, tabun, and soman, [13] [14] have drawn the interest of the U.S. Army . That attention has resulted in the establishment of a biodegradation program in search of safe and effective means of ...

  4. Nerve agent - Wikipedia

    en.wikipedia.org/wiki/Nerve_agent

    The reaction product of the most important nerve agents, including Soman, Sarin, Tabun and VX, with acetylcholinesterase were solved by the U.S. Army using X-ray crystallography in the 1990s. [ 10 ] [ 11 ] The reaction products have been confirmed subsequently using different sources of acetylcholinesterase and the closely related target enzyme ...

  5. VX (nerve agent) - Wikipedia

    en.wikipedia.org/wiki/VX_(nerve_agent)

    However, compared with other highly toxic nerve agents like soman or sarin, VX undergoes relatively slow "aging". Aging is a time-dependent side reaction (loss of an alkoxyl group) that occurs on nerve agents after phosphorylation and renders the nerve agent-acetylcholinesterase complex highly resistant to regeneration by any known antidote.

  6. Dicyclohexyl phosphorofluoridate - Wikipedia

    en.wikipedia.org/wiki/Dicyclohexyl_phosphoro...

    It's a colorless liquid that is extremely resistant to hydrolysis. [3] DCFP can be produced by reaction of cyclohexanol with phosphoryl dichloride fluoride. [2] [3 ...

  7. Sarin - Wikipedia

    en.wikipedia.org/wiki/Sarin

    The most important chemical reactions of phosphoryl halides is the hydrolysis of the bond between phosphorus and the fluorine atom. This P-F bond is easily broken by nucleophilic agents, such as water and hydroxide. At high pH, sarin decomposes rapidly to nontoxic phosphonic acid derivatives.

  8. Butyrylcholinesterase - Wikipedia

    en.wikipedia.org/wiki/Butyrylcholinesterase

    590 12038 Ensembl ENSG00000114200 ENSMUSG00000027792 UniProt P06276 Q03311 RefSeq (mRNA) NM_000055 NM_009738 RefSeq (protein) NP_000046 NP_033868 Location (UCSC) Chr 3: 165.77 – 165.84 Mb Chr 3: 73.54 – 73.62 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Butyrylcholinesterase (HGNC symbol BCHE ; EC 3.1.1.8), also known as BChE, BuChE, BuChase, pseudocholinesterase, or plasma ...

  9. Pinacolyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Pinacolyl_alcohol

    This article about an alcohol is a stub. You can help Wikipedia by expanding it.