Abstract
Nerve agents such as sarin, VX and tabun are organophosphorus compounds able to inhibit an enzyme acetylcholinesterase (AChE). AChE reactivators and anticholinergics are generally used as antidotes in the case of intoxication with these agents. None from the known AChE reactivators is able to reactivate AChE inhibited by all kinds of nerve agents. In this work, reactivation potency of seventeen structurally different AChE reactivators was tested in vitro and subsequently, relationship between their chemical structure and biological activity was outlined. VX was chosen as appropriate member of the nerve agent family.
Keywords: Nerve agent, VX, Reactivation, Acetylcholinesterase, Oxime.
Medicinal Chemistry
Title:Structure-Activity Relationship for the Reactivators of Acetylcholinesterase Inhibited by Nerve Agent VX
Volume: 9 Issue: 5
Author(s): Kamil Kuca, Kamil Musilek, Daniel Jun, Jana Karasova, Ondrej Soukup, Jaroslav Pejchal and Martina Hrabinova
Affiliation:
Keywords: Nerve agent, VX, Reactivation, Acetylcholinesterase, Oxime.
Abstract: Nerve agents such as sarin, VX and tabun are organophosphorus compounds able to inhibit an enzyme acetylcholinesterase (AChE). AChE reactivators and anticholinergics are generally used as antidotes in the case of intoxication with these agents. None from the known AChE reactivators is able to reactivate AChE inhibited by all kinds of nerve agents. In this work, reactivation potency of seventeen structurally different AChE reactivators was tested in vitro and subsequently, relationship between their chemical structure and biological activity was outlined. VX was chosen as appropriate member of the nerve agent family.
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Cite this article as:
Kuca Kamil, Musilek Kamil, Jun Daniel, Karasova Jana, Soukup Ondrej, Pejchal Jaroslav and Hrabinova Martina, Structure-Activity Relationship for the Reactivators of Acetylcholinesterase Inhibited by Nerve Agent VX, Medicinal Chemistry 2013; 9 (5) . https://dx.doi.org/10.2174/1573406411309050008
DOI https://dx.doi.org/10.2174/1573406411309050008 |
Print ISSN 1573-4064 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6638 |
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