Summary:
The ability of the oxime HS-6 [1-(4-hydroxyiminomethylpyridinium)-3-(4-carbamoylpyridinium)-2-
-oxa-propane dichloride] to reactive in vitro the enzyme acetylcholinesterase inhibited by the nerve
agent sarin [O-isopropylmethylfluorophosphonate] was evaluated. The reactivators 2-PAM [2-hydroxyiminomethyl-
1-methylpyridinium chloride], toxogonin [1,3-bis(4-hydroxyiminomethylpyridinium)-
2-oxa-propane dichloride] and H-oxime HI-6 [1-(2-hydroxyiminomethylpyridinium)-
-3-(4-carbamoylpyridinium)-2-oxa-propane dichloride] were chosen for comparison. The oxime HS-6
was an effective reactivator of sarin-inhibited AChE. It is not as effective as the H-oxime HI-6, but
it is better than 2-PAM and obidoxime.
Key words:
acetylcholinesterase – sarin – HS-6 – HI-6 – obidoxime – 2-PAM – in vitro
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