Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
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Peroxidase activity and structural transitions of cytochrome c bound to cardiolipin-containing membranesL-trans-Epoxysuccinyl-leucylamido(4-guanidino)butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and LComparison of methods for analyzing kinetic data from mechanism-based enzyme inactivation: application to nitric oxide synthaseMonoacylglycerol lipase - a target for drug development?Evaluation of a Brain Acetylcholinesterase Extraction Method and Kinetic Constants after Methyl-Paraoxon Inhibition in Three Brazilian Fish SpeciesStructural Basis for the Inactivation of Thermus thermophilus Proline Dehydrogenase by N- Propargylglycine † , ‡Probing the Active Center of Benzaldehyde Lyase with Substitutions and the Pseudosubstrate Analogue Benzoylphosphonic Acid Methyl Ester †The Structure of the Proline Utilization A Proline Dehydrogenase Domain Inactivated by N -Propargylglycine Provides Insight into Conformational Changes Induced by Substrate Binding and Flavin Reduction ,Inhibition of the PLP-dependent enzyme serine palmitoyltransferase by cycloserine: evidence for a novel decarboxylative mechanism of inactivationReaction of Cresyl Saligenin Phosphate, the Organophosphorus Agent Implicated in Aerotoxic Syndrome, with Human Cholinesterases: Mechanistic Studies Employing Kinetics, Mass Spectrometry, and X-ray Structure AnalysisStructural Framework for Covalent Inhibition of Clostridium botulinum Neurotoxin A by Targeting Cys165Piperidinols That Show Anti-Tubercular Activity as Inhibitors of Arylamine N-Acetyltransferase: An Essential Enzyme for Mycobacterial Survival Inside MacrophagesDiscovery of Novel Irreversible Inhibitors of Interleukin (IL)-2-inducible Tyrosine Kinase (Itk) by Targeting Cysteine 442 in the ATP PocketKinetic, Mutational, and Structural Studies of the Venezuelan Equine Encephalitis Virus Nonstructural Protein 2 Cysteine ProteaseCharacterization of a novel dithiocarbamate glutathione reductase inhibitor and its use as a tool to modulate intracellular glutathione.Key Targets for Multi-Target Ligands Designed to Combat NeurodegenerationSynthesis of chloromethyl ketone derivatives of fatty acids. Their use as specific inhibitors of acetoacetyl-coenzyme A thiolase, cholesterol biosynthesis and fatty acid synthesisSelective inhibition of cholesterol synthesis by cell-free preparations of rat liver by using inhibitors of cytoplasmic acetoacetyl-coenzyme A thiolaseThe irreversible binding of acetylcholine mustard to muscarinic receptors in intestinal smooth muscle of the guinea-pigA three-step kinetic mechanism for selective inhibition of cyclo-oxygenase-2 by diarylheterocyclic inhibitorsThe synthesis of lysylfluoromethanes and their properties as inhibitors of trypsin, plasmin and cathepsin BSynthesis and properties of peptidyl derivatives of arginylfluoromethanesCatalytic irreversible inhibition of bacterial and plant arginine decarboxylase activities by novel substrate and product analoguesActive-site directed inactivation of rat ovarian 20 alpha-hydroxysteroid dehydrogenaseThe synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinasesIrreversible inhibition of delta 5-3-oxosteroid isomerase by 2-substituted progesteronesInteraction of benzilylcholine mustard, benzilylcholine and lachesine with the histamine receptor in the longitudinal muscle of guinea-pig ileumN-(5'-phosphopyridoxyl)glutamic acid and N-(5'-phosphopyridoxyl)-2-oxopyrrolidine-5-carboxylic acid and their action on the apoenzyme of aspartate aminotransferaseMuscarinic receptors in rat sympathetic gangliaInactivation of delta 5-3-oxo steroid isomerase with active-site-directed acetylenic steroidsAlkyl selenosulphates (seleno Bunte salts). A new class of thiol-blocking reagentsOltipraz, an inhibitor of human immunodeficiency virus type 1 replicationThioredoxin glutathione reductase from Schistosoma mansoni: an essential parasite enzyme and a key drug targetBiochemical and mass spectrometric characterization of human N-acylethanolamine-hydrolyzing acid amidase inhibitionKinetic and mechanistic characterization of the glyceraldehyde 3-phosphate dehydrogenase from Mycobacterium tuberculosisCharacterization of the inactivation of rat fatty acid synthase by C75: inhibition of partial reactions and protection by substratesInhibition of chymotrypsin by heparin cofactor IILSD1 Histone Demethylase Assays and InhibitionCovalent Modifiers: A Chemical Perspective on the Reactivity of α,β-Unsaturated Carbonyls with Thiols via Hetero-Michael Addition ReactionsKinetics of the reaction of streptokinase-plasmin complex with purified human and mouse alpha 2-macroglobulin. Implications for mechanism.
P2860
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P2860
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
description
1962 nî lūn-bûn
@nan
1962 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1962 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1962年の論文
@ja
1962年論文
@yue
1962年論文
@zh-hant
1962年論文
@zh-hk
1962年論文
@zh-mo
1962年論文
@zh-tw
1962年论文
@wuu
name
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@ast
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@en
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@nl
type
label
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@ast
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@en
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@nl
prefLabel
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@ast
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@en
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase.
@nl
P1476
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase
@en
P2093
P304
P407
P577
1962-10-01T00:00:00Z