Mechanism of interaction of novel uncharged, centrally active reactivators with OP-hAChE conjugates.
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P. Taylor | V. Fokin | Z. Kovarik | Z. Radić | Rakesh K. Sit | G. Amitai | S. Berend | Edzna S Garcia | Limin Zhang | K. Barry Sharpless
[1] P. Taylor,et al. Refinement of Structural Leads for Centrally Acting Oxime Reactivators of Phosphylated Cholinesterases* , 2012, The Journal of Biological Chemistry.
[2] J. Cashman,et al. Nonquaternary reactivators for organophosphate-inhibited cholinesterases. , 2012, Journal of medicinal chemistry.
[3] D. Noort,et al. Peripheral site ligand conjugation to a non-quaternary oxime enhances reactivation of nerve agent-inhibited human acetylcholinesterase. , 2011, Toxicology letters.
[4] P. Renard,et al. First efficient uncharged reactivators for the dephosphylation of poisoned human acetylcholinesterase. , 2011, Chemical communications.
[5] J. Cashman,et al. Amidine-oximes: reactivators for organophosphate exposure. , 2011, Journal of medicinal chemistry.
[6] P. Taylor,et al. New Structural Scaffolds for Centrally Acting Oxime Reactivators of Phosphylated Cholinesterases* , 2011, The Journal of Biological Chemistry.
[7] R. K. Gordon,et al. Pro-2-PAM therapy for central and peripheral cholinesterases. , 2010, Chemico-biological interactions.
[8] J. Olson,et al. Novel oximes as blood-brain barrier penetrating cholinesterase reactivators. , 2010, Chemico-biological interactions.
[9] G. Amitai,et al. Asymmetric fluorogenic organophosphates for the development of active organophosphate hydrolases with reversed stereoselectivity. , 2007, Toxicology.