Page last updated: 2024-08-23

vx and echothiophate iodide

vx has been researched along with echothiophate iodide in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eldefrawi, AT; Eldefrawi, ME; Silveira, CL1
Broomfield, CA; Lockridge, O; Millard, CB1
Barak, D; Pittel, Z; Segall, Y1
Carletti, E; Lockridge, O; Masson, P; Nachon, F; Nicolet, Y; Schopfer, LM; Wandhammer, M1

Other Studies

4 other study(ies) available for vx and echothiophate iodide

ArticleYear
Putative M2 muscarinic receptors of rat heart have high affinity for organophosphorus anticholinesterases.
    Toxicology and applied pharmacology, 1990, Volume: 103, Issue:3

    Topics: Animals; Cholinesterase Inhibitors; Dioxolanes; Dose-Response Relationship, Drug; Echothiophate Iodide; Insecticides; Male; Myocardium; Organophosphates; Organophosphorus Compounds; Organothiophosphorus Compounds; Paraoxon; Parasympathomimetics; Rats; Rats, Inbred Strains; Receptors, Muscarinic; Sarin; Soman; Tritium

1990
Protein engineering of a human enzyme that hydrolyzes V and G nerve agents: design, construction and characterization.
    Chemico-biological interactions, 1999, May-14, Volume: 119-120

    Topics: Animals; Benzoylcholine; Binding Sites; Butyrylcholinesterase; Butyrylthiocholine; Cephamycins; Chemical Warfare Agents; Cholinesterase Inhibitors; Drug Design; Echothiophate Iodide; Humans; Hydrolysis; Inactivation, Metabolic; Kinetics; Mutagenesis, Site-Directed; Organophosphates; Organothiophosphorus Compounds; Protein Engineering; Sarin; Soman; Torpedo

1999
Function-specific blockage of M(1) and M(3) muscarinic acetylcholine receptors by VX and echothiophate.
    Brain research, 2006, Apr-26, Volume: 1085, Issue:1

    Topics: Animals; Atropine; CHO Cells; Cholinesterase Inhibitors; Colforsin; Cricetinae; Cyclic AMP; Dose-Response Relationship, Drug; Drug Interactions; Echothiophate Iodide; Muscarinic Agonists; Muscarinic Antagonists; N-Methylscopolamine; Organothiophosphorus Compounds; Oxotremorine; Phosphatidylinositols; Protein Binding; Receptor, Muscarinic M1; Receptor, Muscarinic M3; Transfection; Tritium

2006
X-ray crystallographic snapshots of reaction intermediates in the G117H mutant of human butyrylcholinesterase, a nerve agent target engineered into a catalytic bioscavenger.
    The Biochemical journal, 2011, Feb-15, Volume: 434, Issue:1

    Topics: Amino Acid Substitution; Butyrylcholinesterase; Catalytic Domain; Crystallography, X-Ray; Echothiophate Iodide; Gene Expression Regulation, Enzymologic; Humans; Models, Molecular; Molecular Structure; Mutagenesis, Site-Directed; Organophosphorus Compounds; Organothiophosphorus Compounds; Protein Engineering; Receptors, Fc

2011