Abstract
Two promising uncharged reactivators for inhibited human BChE and AChE have been described. These compounds show an ability to reactivate VX-inhibited BChE largely superior to those of known pyridinium aldoximes. Moreover, these oximes also exhibit a good ability to reactivate VX-, tabun- and paraoxon-inhibited human AChE.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylcholinesterase / metabolism*
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Butyrylcholinesterase / metabolism*
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Carbolines / chemical synthesis
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Carbolines / chemistry
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Carbolines / pharmacology*
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Cholinesterase Inhibitors / chemical synthesis
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Cholinesterase Inhibitors / chemistry
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Cholinesterase Inhibitors / pharmacology*
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Humans
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Molecular Structure
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Oximes / chemical synthesis
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Oximes / chemistry
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Oximes / pharmacology*
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Phosphorylation / drug effects
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Structure-Activity Relationship
Substances
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Carbolines
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Cholinesterase Inhibitors
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Oximes
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Acetylcholinesterase
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Butyrylcholinesterase