Search details
1.
Detoxification of V-Nerve Agents Assisted by a Microperoxidase: New Pathway Revealed by the Use of a Relevant VX Simulant.
Chembiochem
; : e202400137, 2024 Apr 09.
Article
in English
| MEDLINE | ID: mdl-38591336
2.
Rapid discovery and crystallography study of highly potent and selective butylcholinesterase inhibitors based on oxime-containing libraries and conformational restriction strategies.
Bioorg Chem
; 134: 106465, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36933339
3.
Grid-Type Quaternary Metallosupramolecular Compounds Inhibit Human Cholinesterases through Dynamic Multivalent Interactions.
Chembiochem
; 23(23): e202200456, 2022 12 05.
Article
in English
| MEDLINE | ID: mdl-36193860
4.
Diisopropylfluorophosphate-induced status epilepticus drives complex glial cell phenotypes in adult male mice.
Neurobiol Dis
; 152: 105276, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33529768
5.
Characterization of four BCHE mutations associated with prolonged effect of suxamethonium.
Pharmacogenomics J
; 21(2): 165-173, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33024248
6.
Enantioseparation, in vitro testing, and structural characterization of triple-binding reactivators of organophosphate-inhibited cholinesterases.
Biochem J
; 477(15): 2771-2790, 2020 08 14.
Article
in English
| MEDLINE | ID: mdl-32639532
7.
A Thermophilic Bacterial Esterase for Scavenging Nerve Agents: A Kinetic, Biophysical and Structural Study.
Molecules
; 26(3)2021 Jan 27.
Article
in English
| MEDLINE | ID: mdl-33513869
8.
Rapid discovery of a selective butyrylcholinesterase inhibitor using structure-based virtual screening.
Bioorg Med Chem Lett
; 30(24): 127609, 2020 12 15.
Article
in English
| MEDLINE | ID: mdl-33039562
9.
Development of potent reversible selective inhibitors of butyrylcholinesterase as fluorescent probes.
J Enzyme Inhib Med Chem
; 35(1): 498-505, 2020 Dec.
Article
in English
| MEDLINE | ID: mdl-31914836
10.
N-Propargylpiperidines with naphthalene-2-carboxamide or naphthalene-2-sulfonamide moieties: Potential multifunctional anti-Alzheimer's agents.
Bioorg Med Chem
; 25(2): 633-645, 2017 01 15.
Article
in English
| MEDLINE | ID: mdl-27908752
11.
Bacterial Expression of Human Butyrylcholinesterase as a Tool for Nerve Agent Bioscavengers Development.
Molecules
; 22(11)2017 Oct 27.
Article
in English
| MEDLINE | ID: mdl-29077024
12.
Comparison of the Binding of Reversible Inhibitors to Human Butyrylcholinesterase and Acetylcholinesterase: A Crystallographic, Kinetic and Calorimetric Study.
Molecules
; 22(12)2017 Nov 29.
Article
in English
| MEDLINE | ID: mdl-29186056
13.
Crystal structure of the vaccinia virus DNA polymerase holoenzyme subunit D4 in complex with the A20 N-terminal domain.
PLoS Pathog
; 10(3): e1003978, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24603707
14.
Structure-based development of nitroxoline derivatives as potential multifunctional anti-Alzheimer agents.
Bioorg Med Chem
; 23(15): 4442-4452, 2015 Aug 01.
Article
in English
| MEDLINE | ID: mdl-26116179
15.
Three conserved histidine residues contribute to mitochondrial iron transport through mitoferrins.
Biochem J
; 460(1): 79-89, 2014 May 15.
Article
in English
| MEDLINE | ID: mdl-24624902
16.
An EPR/HYSCORE, Mössbauer, and resonance Raman study of the hydrogenase maturation enzyme HydF: a model for N-coordination to [4Fe-4S] clusters.
J Biol Inorg Chem
; 19(1): 75-84, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24240692
17.
Warfare Nerve Agents and Paraoxonase-1 as a Potential Prophylactic Therapy against Intoxication.
Protein Pept Lett
; 2024 May 03.
Article
in English
| MEDLINE | ID: mdl-38706353
18.
Inhibition of Human Cholinesterases and inâ vitro ß-Amyloid Aggregation by Rationally Designed Peptides.
ChemMedChem
; 18(12): e202200691, 2023 06 15.
Article
in English
| MEDLINE | ID: mdl-36995341
19.
Pseudo-irreversible butyrylcholinesterase inhibitors: Structure-activity relationships, computational and crystallographic study of the N-dialkyl O-arylcarbamate warhead.
Eur J Med Chem
; 247: 115048, 2023 Feb 05.
Article
in English
| MEDLINE | ID: mdl-36586299
20.
Discovery of new, highly potent and selective inhibitors of BuChE - design, synthesis, in vitro and in vivo evaluation and crystallography studies.
Eur J Med Chem
; 249: 115135, 2023 Mar 05.
Article
in English
| MEDLINE | ID: mdl-36696766