44 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 35526478 | Halogen substituents enhance oxime nucleophilicity for reactivation of cholinesterases inhibited by nerve agents. | 2022 Aug 5 | 1 |
2 | 32305437 | Structural and kinetic evidence of aging after organophosphate inhibition of human Cathepsin A. | 2020 Jul | 1 |
3 | 32454005 | Synthesis and in vitro evaluation of novel non-oximes for the reactivation of nerve agent inhibited human acetylcholinesterase. | 2020 Aug 1 | 1 |
4 | 32583098 | Targeting organophosphorus compounds poisoning by novel quinuclidine-3 oximes: development of butyrylcholinesterase-based bioscavengers. | 2020 Sep | 1 |
5 | 30858091 | The arrhythmogenic potential of nerve agents and a cardiac safety profile of antidotes - A proof-of-concept study using human induced pluripotent stem cells derived cardiomyocytes (hiPSC-CM). | 2019 Jun 15 | 1 |
6 | 30096649 | Discovery of a potent non-oxime reactivator of nerve agent inhibited human acetylcholinesterase. | 2018 Sep 5 | 2 |
7 | 30312685 | Interactions between acetylcholinesterase, toxic organophosphorus compounds and a short series of structurally related non-oxime reactivators: Analysis of reactivation and inhibition kinetics in vitro. | 2018 Dec 15 | 1 |
8 | 30383374 | Pyridinium Oximes with Ortho-Positioned Chlorine Moiety Exhibit Improved Physicochemical Properties and Efficient Reactivation of Human Acetylcholinesterase Inhibited by Several Nerve Agents. | 2018 Dec 13 | 1 |
9 | 26210933 | Investigation of the reactivation kinetics of a large series of bispyridinium oximes with organophosphate-inhibited human acetylcholinesterase. | 2016 Feb 26 | 1 |
10 | 27238725 | Design and synthesis of N-substituted-2-hydroxyiminoacetamides and interactions with cholinesterases. | 2016 Nov 25 | 1 |
11 | 25522658 | Effect of reversible ligands on oxime-induced reactivation of sarin- and cyclosarin-inhibited human acetylcholinesterase. | 2015 Feb 3 | 1 |
12 | 24443939 | Exploring the physicochemical properties of oxime-reactivation therapeutics for cyclosarin, sarin, tabun, and VX inactivated acetylcholinesterase. | 2014 Jan 21 | 2 |
13 | 24630558 | Design, synthesis, and characterization of novel, nonquaternary reactivators of GF-inhibited human acetylcholinesterase. | 2014 Apr 1 | 2 |
14 | 22975155 | Mechanism of interaction of novel uncharged, centrally active reactivators with OP-hAChE conjugates. | 2013 Mar 25 | 1 |
15 | 22982773 | A common mechanism for resistance to oxime reactivation of acetylcholinesterase inhibited by organophosphorus compounds. | 2013 Mar 25 | 2 |
16 | 23376121 | Catalytic-site conformational equilibrium in nerve-agent adducts of acetylcholinesterase: possible implications for the HI-6 antidote substrate specificity. | 2013 May 1 | 2 |
17 | 23789829 | In silico pharmacophore modeling on known pyridinium oxime reactivators of cyclosarin (GF) inhibited AChE to Aid discovery of potential, more efficacious novel non-oxime reactivators. | 2013 Sep | 2 |
18 | 22343626 | Refinement of structural leads for centrally acting oxime reactivators of phosphylated cholinesterases. | 2012 Apr 6 | 1 |
19 | 22520752 | Evolved stereoselective hydrolases for broad-spectrum G-type nerve agent detoxification. | 2012 Apr 20 | 1 |
20 | 22561105 | Kinetic interactions of a homologous series of bispyridinium monooximes (HGG oximes) with native and phosphonylated human acetylcholinesterase. | 2012 Jul 7 | 1 |
21 | 21217689 | Directed evolution of hydrolases for prevention of G-type nerve agent intoxication. | 2011 Feb | 1 |
22 | 21930118 | Reactivation of organophosphate-inhibited human acetylcholinesterase by isonitrosoacetone (MINA): a kinetic analysis. | 2011 Nov 15 | 1 |
23 | 22238531 | Highly efficient cyclosarin degradation mediated by a β-cyclodextrin derivative containing an oxime-derived substituent. | 2011 | 1 |
24 | 20192902 | Oxime K027: novel low-toxic candidate for the universal reactivator of nerve agent- and pesticide-inhibited acetylcholinesterase. | 2010 Aug | 1 |
25 | 20510679 | Kinetic analysis of interactions between alkylene-linked bis-pyridiniumaldoximes and human acetylcholinesterases inhibited by various organophosphorus compounds. | 2010 Sep 15 | 3 |
26 | 20888357 | Reactivation of organophosphate-inhibited human, Cynomolgus monkey, swine and guinea pig acetylcholinesterase by MMB-4: a modified kinetic approach. | 2010 Dec 15 | 1 |
27 | 18565503 | Reactivation of DFP- and paraoxon-inhibited acetylcholinesterases by pyridinium oximes. | 2008 Sep 25 | 2 |
28 | 18588863 | Characterization of asymmetric fluorogenic phosphonates as probes for developing organophosphorus hydrolases with broader stereoselectivity. | 2008 Sep 25 | 1 |
29 | 20020898 | In Vitro Comparison of Two Most Promising H-Oximes (HI-6 and HLö-7) and Currently Commercially Available Reactivators Pralidoxime and Obidoxime in Reactivation of Cyclosarin-Inhibited Human Cholinesterases. | 2008 | 1 |
30 | 17112559 | Recent advances in evaluation of oxime efficacy in nerve agent poisoning by in vitro analysis. | 2007 Mar | 1 |
31 | 17370251 | Reactivation of organophosphate-inhibited human AChE by combinations of obidoxime and HI 6 in vitro. | 2007 Nov-Dec | 1 |
32 | 17503257 | Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin. | 2007 Jun-Aug | 2 |
33 | 17960099 | Targeted synthesis of 1-(4-hydroxyiminomethylpyridinium)-3-pyridiniumpropane dibromide--a new nerve agent reactivator. | 2007 Aug 20 | 2 |
34 | 18045198 | Structural factors influencing potency of currently used acetylcholinesterase reactivators for treatment of cyclosarin intoxications. | 2007 | 3 |
35 | 17194020 | New group of xylene linker-containing acetylcholinesterase reactivators as antidotes against the nerve agent cyclosarin. | 2006 Oct | 5 |
36 | 17438836 | Reactivation potency of new group of acetylcholinesterase reactivators and their comparison with currently available oximes. | 2006 | 3 |
37 | 15911280 | Design and synthesis of new bis-pyridinium oxime reactivators for acetylcholinesterase inhibited by organophosphorous nerve agents. | 2005 Jun 2 | 1 |
38 | 16429489 | Comparison of the potency of newly developed and currently available oximes to reactivate nerve agent-inhibited acetylcholinesterase in vitro and in vivo. | 2005 Dec 15 | 1 |
39 | 14985944 | Effect of organophosphorus hydrolysing enzymes on obidoxime-induced reactivation of organophosphate-inhibited human acetylcholinesterase. | 2004 Jun | 1 |
40 | 15544060 | A comparison of the efficacy of a bispyridinium oxime--1,4-bis-(2-hydroxyiminomethylpyridinium) butane dibromide and currently used oximes to reactivate sarin, tabun or cyclosarin-inhibited acetylcholinesterase by in vitro methods. | 2004 Oct | 1 |
41 | 15568733 | 1,3-Bis(2-hydroxyiminomethylpyridinium) propane as the potential reactivator of the acetylcholinesterase inhibited by nerve agents. | 2004 | 2 |
42 | 12373455 | Equipotent cholinesterase reactivation in vitro by the nerve agent antidotes HI 6 dichloride and HI 6 dimethanesulfonate. | 2002 Oct | 1 |
43 | 9587020 | Reactivating potency of obidoxime, pralidoxime, HI 6 and HLö 7 in human erythrocyte acetylcholinesterase inhibited by highly toxic organophosphorus compounds. | 1998 Mar | 2 |
44 | 9806430 | Inhibition, reactivation and aging kinetics of cyclohexylmethylphosphonofluoridate-inhibited human cholinesterases. | 1998 Sep | 1 |