Search Results - "Ashani, Y"
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Stereo-specific synthesis of analogs of nerve agents and their utilization for selection and characterization of paraoxonase (PON1) catalytic scavengers
Published in Chemico-biological interactions (06-09-2010)“…Fluorogenic organophosphate inhibitors of acetylcholinesterase (AChE) homologous in structure to nerve agents provide useful probes for high throughput…”
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Laboratory Setup for Long-Term Monitoring of the Volatilization of Hazardous Materials: Preliminary Tests of O-Ethyl S-2-(N,N-Diisopropylamino)ethyl Methylphosphonothiolate on Asphalt
Published in Environmental science & technology (01-04-2004)“…Contrary to commonly used pesticides, the rate of volatilization of extremely toxic chemicals such as the nerve agent O-ethyl S-2-(N,N-diisopropylamino)ethyl…”
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The impact of molecular variants, crystallization conditions and space group on the structure-based drug design field
Published in Acta crystallographica. Section A, Foundations and advances (22-08-2023)“…Abstract only…”
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Prevention of soman-induced cognitive deficits by pretreatment with human butyrylcholinesterase in rats
Published in Pharmacology, biochemistry and behavior (01-12-1993)“…This study examined the ability of pretreatment with human serum butyrylcholinesterase (HuBChE) to prevent soman-induced cognitive impairments. Behavioral…”
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Role of tyrosine 337 in the binding of huperzine A to the active site of human acetylcholinesterase
Published in Molecular pharmacology (01-03-1994)“…Huperzine A (HUP), a natural, potent, 'slow,' reversible inhibitor of antiacetylcholinesterase (AChE), has been suggested to be superior to…”
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Estimation of the Upper Limit of Human Butyrylcholinesterase Dose Required for Protection against Organophosphates Toxicity: a Mathematically Based Toxicokinetic Model
Published in Toxicological sciences (01-02-2004)“…Human butyrylcholinesterase (HuBChE) is a drug candidate for protection against organophosphates (OP) intoxication. A mathematically based model was validated…”
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Refined crystal structures of "aged" and "non-aged" organophosphoryl conjugates of gamma-chymotrypsin
Published in Journal of molecular biology (05-10-1991)“…"Aged" organophosphoryl conjugates of serine hydrolases differ from the corresponding "non-aged" conjugates in their striking resistance to nucleophilic…”
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Inhibition of cholinesterases with cationic phosphonyl oximes highlights distinctive properties of the charged pyridine groups of quaternary oxime reactivators
Published in Biochemical pharmacology (15-07-2003)“…Oxime-induced reactivation of phosphonylated cholinesterases (ChEs) produces charged phosphonyl pyridine oxime intermediates (POXs) that are most potent…”
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Direct observation and elucidation of the structures of aged and nonaged phosphorylated cholinesterases by phosphorus-31 NMR spectroscopy
Published in Biochemistry (Easton) (01-12-1993)Get full text
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Conformational differences between aged and nonaged pyrenebutyl-containing organophosphoryl conjugates of chymotrypsin as detected by optical spectroscopy
Published in Biochemistry (Easton) (07-02-1989)“…Homologous aged and nonaged fluorescent organophosphorus conjugates of alpha-chymotrypsin (Cht) were used in a comparative spectroscopic study of the…”
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Prospective of human butyrylcholinesterase as a detoxifying antidote and potential regulator of controlled-release drugs
Published in Drug development research (01-07-2000)“…Butyrylcholinesterase from human plasma (HuBChE) is a potential drug candidate that can be employed in several therapeutic fields. This is attributed to the…”
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The Stoichiometry of Protection against Soman and VX Toxicity in Monkeys Pretreated with Human Butyrylcholinesterase
Published in Toxicology and applied pharmacology (01-07-1997)“…Bioscavengers of organophophates (OP) have been examined as potential substitutes for the currently approved drug treatment against OP toxicity. The present…”
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Design, expression and characterization of mutants of fasciculin optimized for interaction with its target, acetylcholinesterase
Published in Protein engineering, design and selection (01-10-2009)“…Predicting mutations that enhance protein–protein affinity remains a challenging task, especially for high-affinity complexes. To test our capability to…”
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Tritium labeling of a powerful methylphosphonate inhibitor of cholinesterase: synthesis and biological applications
Published in Analytical biochemistry (15-02-1988)“…7-(Methylethoxy phosphinyloxy)-1-methyl-quinolinium iodide (MEPQ), a powerful anti-cholinesterase methylphosphonate ester, was labeled with tritium (9 Ci/mmol)…”
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Formation of an unstable covalent intermediate during the inhibition of electric-eel acetylcholinesterase with 1,3,2-dioxaphosphorinane 2-oxides
Published in Biochemical journal (01-03-1979)“…The kinetics of interaction of eel acetylcholinesterase (EC 3.1.1.7) with 1,3,2-dioxaphosphorinane 2-oxides were investigated. It was demonstrated that the…”
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In vitro and in vivo protection of acetylcholinesterase against organophosphate poisoning by pretreatment with a novel derivative of 1,3,2-dioxaphosphorinane 2-oxide
Published in Journal of medicinal chemistry (01-02-1983)“…Covalent molecular combinations of a cyclic phosphate (dioxaphosphorinane) and a potential leaving group, such as 3-(trimethylammonio)phenol iodide (TMPH),…”
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Laboratory setup for long-term monitoring of the volatilization of hazardous materials
Published in Environmental science & technology (01-04-2004)“…Contrary to commonly used pesticides, the rate of volatilization of extremely toxic chemicals such as the nerve agent O-ethyl S-2-(N,N-diisopropylamino) ethyl…”
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Prophylaxis against Soman Inhalation Toxicity in Guinea Pigs by Pretreatment Alone with Human Serum Butyrylcholinesterase
Published in Toxicological sciences (01-06-1998)“…Human butyrylcholinesterase (HuBChE) has previously been shown to protect mice, rats, and monkeys against multiple lethal toxic doses of organophosphorus (OP)…”
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