Journal of Medicinal Chemistry p. 7034 - 7042 (2018)
Update date:2022-08-11
Topics:
Zhuang, Qinggeng
Franjesevic, Andrew J.
Corrigan, Thomas S.
Coldren, William H.
Dicken, Rachel
Sillart, Sydney
Deyong, Ashley
Yoshino, Nathan
Smith, Justin
Fabry, Stephanie
Fitzpatrick, Keegan
Blanton, Travis G.
Joseph, Jojo
Yoder, Ryan J.
McElroy, Craig A.
Ekici, ?zlem Dogan
Callam, Christopher S.
Hadad, Christopher M.
After the inhibition of acetylcholinesterase (AChE) by organophosphorus (OP) nerve agents, a dealkylation reaction of the phosphylated serine, referred to as aging, can occur. When aged, known reactivators of OP-inhibited AChE are no longer effective. Realkylation of aged AChE may provide a route to reversing aging. We designed and synthesized a library of quinone methide precursors (QMPs) as proposed realkylators of aged AChE. Our lead compound (C8) from an in vitro screen successfully resurrected 32.7 and 20.4% of the activity of methylphosphonate-aged and isopropyl phosphate-aged electric-eel AChE, respectively, after 4 days. C8 displays properties of both resurrection (recovery from the aged to the native state) and reactivation (recovery from the inhibited to the native state). Resurrection of methylphosphonate-aged AChE by C8 was significantly pH-dependent, recovering 21% of activity at 4 mM and pH 9 after only 1 day. C8 is also effective against isopropyl phosphate-aged human AChE.
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