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Paper Text
Almenares-Lopez_2019_Chem.Biol.Interact_13ChEPon_308_252 Copper(II)-dependent hydrolysis of trichloronate by turkey serum albumin
Antonijevic_2019_Chem.Biol.Interact_13ChEPon_308_385 Comparison of oximes K203 and K027 based on Benchmark dose analysis of rat diaphragmal acetylcholinesterase reactivation
Bigley_2019_Chem.Biol.Interact_13ChEPon_308_80 The evolution of phosphotriesterase for decontamination and detoxification of organophosphorus chemical warfare agents
Bosak_2019_Chem.Biol.Interact_13ChEPon_308_101 Structural aspects of 4-aminoquinolines as reversible inhibitors of human acetylcholinesterase and butyrylcholinesterase
Cai_2019_Chem.Biol.Interact_13ChEPon_310_108756 Dimerization of human butyrylcholinesterase expressed in bacterium for development of a thermally stable bioscavenger of organophosphorus compounds
Cavalcante_2019_Chem.Biol.Interact_13ChEPon_309_108682 Synthesis and in vitro evaluation of neutral aryloximes as reactivators of Electrophorus eel acetylcholinesterase inhibited by NEMP, a VX surrogate
Chandar_2019_Chem.Biol.Interact_13ChEPon_310_108715 Molecular dynamics simulations of the interaction of Mouse and Torpedo acetylcholinesterase with covalent inhibitors explain their differential reactivity: Implications for drug design
Chatonnet_2019_Chem.Biol.Interact_13ChEPon_308_179 An evolutionary perspective on the first disulfide bond in members of the cholinesterase-carboxylesterase (COesterase) family: Possible outcomes for cholinesterase expression in prokaryotes
Chen_2019_Chem.Biol.Interact_13ChEPon_306_89 Development of a long-acting Fc-fused cocaine hydrolase with improved yield of protein expression
da Silva_2019_Chem.Biol.Interact_13ChEPon_307_195 Molecular modelling studies on the interactions of 7-methoxytacrine-4-pyridinealdoxime with VX-inhibited human acetylcholinesterase. A near attack approach to assess different spacer-lengths
de Almeida_2019_Chem.Biol.Interact_13ChEPon_308_113 Surface screening, molecular modeling and in vitro studies on the interactions of aflatoxin M1 and human enzymes acetyl- and butyrylcholinesterase
Gerlits_2019_Chem.Biol.Interact_13ChEPon_ A new crystal form of human acetylcholinesterase for exploratory room-temperature crystallography studies
Grigorenko_2019_Chem.Biol.Interact_13ChEPon_306_138 Computer-designed active human butyrylcholinesterase double mutant with a new catalytic triad
Iqbal_2019_Chem.Biol.Interact_13ChEPon_310_108735 Reactivation potency of two novel oximes (K456 and K733) against paraoxon-inhibited acetyl and butyrylcholinesterase: In silico and in vitro models
Jacevic_2019_Chem.Biol.Interact_13ChEPon_308_312 Interspecies and intergender differences in acute toxicity of K-oximes drug candidates
Jasiecki_2019_Chem.Biol.Interact_13ChEPon_307_154 Haplotypes of butyrylcholinesterase K-variant and their influence on the enzyme activity
Javed_2019_Chem.Biol.Interact_13ChEPon_308_130 Association of status of acetylcholinesterase and ACHE gene 3' UTR variants (rs17228602, rs17228616) with drug addiction vulnerability in pakistani population
Liu_2019_Chem.Biol.Interact_13ChEPon_306_147 Activation of G protein-coupled receptor 30 by flavonoids leads to expression of acetylcholinesterase in cultured PC12cells
Luo_2019_Chem.Biol.Interact_13ChEPon_308_164 Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on acetylcholinesterase during myogenic differentiation of contractile rat primary skeletal muscle cells
Makhaeva_2019_Chem.Biol.Interact_13ChEPon_308_224 Overview of novel multifunctional agents based on conjugates of gamma-carbolines, carbazoles, tetrahydrocarbazoles, phenothiazines, and aminoadamantanes for treatment of Alzheimer's disease
Monroy-Noyola_2019_Chem.Biol.Interact_13ChEPon_310_108727 O-hexyl O-2,5-dichlorophenyl phosphoramidate as a substrate for domestic and sea bird serum A-esterases: Hydrolysis levels, Cu(2+)- and Zn(2+)-dependence and stereoselectivity
Myers_2019_Chem.Biol.Interact_13ChEPon_308_170 Human plasma-derived butyrylcholinesterase is behaviorally safe and effective in cynomolgus macaques (Macaca fascicularis) challenged with soman
Novichkova_2019_Chem.Biol.Interact_13ChEPon_309_108699 The four-helix bundle in cholinesterase dimers: Structural and energetic determinants of stability
Pashirova_2019_Chem.Biol.Interact_13ChEPon_310_108753 Delivery nanosystems based on sterically hindered phenol derivatives containing a quaternary ammonium moiety: Synthesis, cholinesterase inhibition and antioxidant activity
Pereira_2019_Chem.Biol.Interact_13ChEPon_308_323 Development of technologies applied to the biodegradation of warfare nerve agents: Theoretical evidence for asymmetric homogeneous catalysis
Poirier_2019_Chem.Biol.Interact_13ChEPon_306_96 Evaluation of a robust engineered enzyme towards organophosphorus insecticide bioremediation using planarians as biosensors
Polisel_2019_Chem.Biol.Interact_13ChEPon_309_108671 Slight difference in the isomeric oximes K206 and K203 makes huge difference for the reactivation of organophosphorus-inhibited AChE: Theoretical and experimental aspects
Rosenberry_2019_Chem.Biol.Interact_13ChEPon_ Rate-limiting step in the decarbamoylation of acetylcholinesterases with large carbamoyl groups
Sha_2019_Chem.Biol.Interact_13ChEPon_309_108686 Effects of astrocyte conditioned medium on neuronal AChE expression upon 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure
Sinko_2019_Chem.Biol.Interact_13ChEPon_308_216 Assessment of scoring functions and in silico parameters for AChE-ligand interactions as a tool for predicting inhibition potency
Song_2019_Chem.Biol.Interact_13ChEPon_308_339 Inhibition of human carboxylesterases by magnolol: Kinetic analyses and mechanism
Stojan_2019_Chem.Biol.Interact_13ChEPon_308_350 The mechanism and benefit of human butyrylcholinesterase activation by what would otherwise be inhibitors
Taylor_2019_Chem.Biol.Interact_13ChEPon_308_194 Assessment of ionizable, zwitterionic oximes as reactivating antidotal agents for organophosphate exposure
Tekes_2019_Chem.Biol.Interact_13ChEPon_310_108737 Pharmacokinetics of K117 and K127, two novel antidote candidates to treat Tabun poisoning
Vitorovic-Todorovic_2019_Chem.Biol.Interact_13ChEPon_309_108714 The in vitro protective effects of the three novel nanomolar reversible inhibitors of human cholinesterases against irreversible inhibition by organophosphorous chemical warfare agents
Xu_2019_Chem.Biol.Interact_13ChEPon_308_317 Differentiation of erythroblast requires the dimeric form of acetylcholinesterase: Interference with erythropoietin receptor
Zhou_2019_Chem.Biol.Interact_13ChEPon_308_372 Structure-based virtual screening leading to discovery of highly selective butyrylcholinesterase inhibitors with solanaceous alkaloid scaffolds
Zorbaz_2019_Chem.Biol.Interact_13ChEPon_307_16 Butyrylcholinesterase inhibited by nerve agents is efficiently reactivated with chlorinated pyridinium oximes

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