نتایج جستجو برای: reactivators

تعداد نتایج: 133  

Journal: :Epilepsy & Behavior 2017
Alison L. Althaus Hilary S. McCarren Aymen Alqazzaz Cecelia Jackson John H. McDonough Carl D. Smith Ethan Hoffman Rebecca S. Hammond Albert J. Robichaud James J. Doherty

Organophosphorus nerve agents (OPNAs) are irreversible inhibitors of acetylcholinesterase that pose a serious threat to public health because of their use as chemical weapons. Exposure to high doses of OPNAs can dramatically potentiate cholinergic synaptic activity and cause status epilepticus (SE). Current standard of care for OPNA exposure involves treatment with cholinergic antagonists, oxim...

Journal: :Molecules 2017
Maja Katalinić Antonio Zandona Alma Ramić Tamara Zorbaz Ines Primožič Zrinka Kovarik

For the last six decades, researchers have been focused on finding efficient reactivators of organophosphorus compound (OP)-inhibited acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). In this study, we have focused our research on a new oxime scaffold based on the Cinchona structure since it was proven to fit the cholinesterases active site and reversibly inhibit their activity. Thr...

Journal: :Bioengineering & translational medicine 2023

A promising strategy to cure HIV-infected individuals is use latency reversing agents (LRAs) reactivate latent viruses, followed by host clearance of infected reservoir cells. However, reactivation proviruses within cells heterogeneous and often incomplete. This fact limits strategies HIV which may require complete elimination viable virus from all cellular reservoirs. For this reason, understa...

Journal: :The Journal of biological chemistry 2012
Zoran Radić Rakesh K Sit Zrinka Kovarik Suzana Berend Edzna Garcia Limin Zhang Gabriel Amitai Carol Green Bozica Radić Valery V Fokin K Barry Sharpless Palmer Taylor

We present a systematic structural optimization of uncharged but ionizable N-substituted 2-hydroxyiminoacetamido alkylamine reactivators of phosphylated human acetylcholinesterase (hAChE) intended to catalyze the hydrolysis of organophosphate (OP)-inhibited hAChE in the CNS. Starting with the initial lead oxime RS41A identified in our earlier study and extending to the azepine analog RS194B, re...

Journal: :Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2005
Lucie Bartosová Kamil Kuca Gabriela Kunesová

The present study was performed to assess and compare a therapeutic efficacy of obidoxime, HI-6, BI-6 and HS-6 administered in equimolar doses and combined with atropine in cyclosarin-poisoned mice and rats. It was demonstrated that all the therapeutic regimens tested, were able to decrease the cyclosarin-induced toxicity significantly - at least 1.5 times. Higher therapeutic ratios, almost thr...

2011
Miroslav Pohanka Martina Hrabinova Kamil Kuca Jean-Pierre Simonato

Assay of acetylcholinesterase (AChE) activity plays an important role in diagnostic, detection of pesticides and nerve agents, in vitro characterization of toxins and drugs including potential treatments for Alzheimer's disease. These experiments were done in order to determine whether indoxylacetate could be an adequate chromogenic reactant for AChE assay evaluation. Moreover, the results were...

Journal: :Chemico-biological interactions 2013
Donald M Maxwell Karen M Brecht Richard E Sweeney

Administration of oxime therapy is currently the standard approach used to reverse the acute toxicity of organophosphorus (OP) compounds, which is usually attributed to OP inhibition of acetylcholinesterase (AChE). Rate constants for reactivation of OP-inhibited AChE by even the best oximes, such as HI-6 and obidoxime, can vary >100-fold between OP-AChE conjugates that are easily reactivated an...

Journal: :Arhiv za higijenu rada i toksikologiju 2015
Maja Katalinić Nikolina Maček Hrvat Jana Žďárová Karasová Jan Misik Zrinka Kovarik

Even if organophosphorus (OP) nerve agents were banned entirely, their presence would remain a problem as weapons of terror (like in Syria). Oxime antidotes currently used in medical practice still fall short of their therapeutic purpose, as they fail to fully restore the activity of cholinesterases, the main target for OPs. As orphan drugs, these antidotes are tested too seldom for anybody's b...

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