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Detoxification of V‐Nerve Agents Assisted by a Microperoxidase: New Pathway Revealed by the Use of a Relevant VX Simulant.
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- ChemBioChem, 2024, v. 25, n. 15, p. 1, doi. 10.1002/cbic.202400137
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Front Cover: Detoxification of V‐Nerve Agents Assisted by a Microperoxidase: New Pathway Revealed by the Use of a Relevant VX Simulant (ChemBioChem 15/2024).
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- ChemBioChem, 2024, v. 25, n. 15, p. 1, doi. 10.1002/cbic.202481501
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- Article
Detoxification of Chemical Warfare Agents by a Zr‐Based MOF with High Recycling Ability at Physiological pH.
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- ChemNanoMat, 2024, v. 10, n. 8, p. 1, doi. 10.1002/cnma.202400132
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Inhibition of Human Cholinesterases and in vitro β‐Amyloid Aggregation by Rationally Designed Peptides.
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- ChemMedChem, 2023, v. 18, n. 12, p. 1, doi. 10.1002/cmdc.202200691
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Front Cover: Inhibition of Human Cholinesterases and in vitro β‐Amyloid Aggregation by Rationally Designed Peptides (ChemMedChem 12/2023).
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- ChemMedChem, 2023, v. 18, n. 12, p. 1, doi. 10.1002/cmdc.202300289
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Grid‐Type Quaternary Metallosupramolecular Compounds Inhibit Human Cholinesterases through Dynamic Multivalent Interactions.
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- ChemBioChem, 2022, v. 23, n. 23, p. 1, doi. 10.1002/cbic.202200456
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Cover Image.
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- Chemical Biology & Drug Design, 2021, v. 97, n. 5, p. i, doi. 10.1111/cbdd.13717
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Discovery of drug‐like acetylcholinesterase inhibitors by rapid virtual screening of a 6.9 million compound database.
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- Chemical Biology & Drug Design, 2021, v. 97, n. 5, p. 1048, doi. 10.1111/cbdd.13825
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Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases.
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- Antioxidants, 2021, v. 10, n. 2, p. 329, doi. 10.3390/antiox10020329
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A Thermophilic Bacterial Esterase for Scavenging Nerve Agents: A Kinetic, Biophysical and Structural Study.
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- Molecules, 2021, v. 26, n. 3, p. 657, doi. 10.3390/molecules26030657
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Enantioseparation, in vitro testing, and structural characterization of triple-binding reactivators of organophosphate-inhibited cholinesterases.
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- Biochemical Journal, 2020, v. 477, n. 15, p. 2771, doi. 10.1042/BCJ20200192
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Efficacy Assessment of an Uncharged Reactivator of NOP-Inhibited Acetylcholinesterase Based on Tetrahydroacridine Pyridine-Aldoxime Hybrid in Mouse Compared to Pralidoxime.
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- Biomolecules (2218-273X), 2020, v. 10, n. 6, p. 858, doi. 10.3390/biom10060858
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Rivastigmine and metabolite analogues with putative Alzheimer's disease-modifying properties in a Caenorhabditis elegans model.
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- Communications Chemistry, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42004-019-0133-4
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RECIPES TO DESIGN SPECIFIC LIGANDS OF HUMAN BUTYRYLCHOLINESTERASE.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 8
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PROKARYOTIC EXPRESSION OF HUMAN BUTYRYLCHOLINESTERASE AS A TOOL FOR CATALYTIC BIOSCAVENGER DEVELOPMENT.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 37
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CRYSTAL STRUCTURES OF HUMAN CHOLINESTERASES IN COMPLEX WITH SUPRAMOLECULAR LIGANDS.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 50
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EVOLUTION OF THE FIRST DISULFIDE BOND IN THE CHOLINESTERASE- CARBOXYLESTERASE (COESTERASE) FAMILY: POSSIBLE CONSEQUENCES FOR CHOLINESTERASE EXPRESSION IN PROKARYOTES.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 55
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BUTYRYLCHOLINESTERASE INHIBITORS GRAFTED WITH ANTIOXIDANT AND NEUROPROTECTIVE ACTIVITIES: NOVEL MULTIFUNCTIONAL LIGANDS FOR ALZHEIMER'S DISEASE.
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- Military Medical Science Letters / Vojenské zdravotnické Listy, 2018, v. 87, p. 127
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Comparison of the Binding of Reversible Inhibitors to Human Butyrylcholinesterase and Acetylcholinesterase: A Crystallographic, Kinetic and Calorimetric Study.
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- Molecules, 2017, v. 22, n. 12, p. 2098, doi. 10.3390/molecules22122098
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Bacterial Expression of Human Butyrylcholinesterase as a Tool for Nerve Agent Bioscavengers Development.
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- Molecules, 2017, v. 22, n. 11, p. 1828, doi. 10.3390/molecules22111828
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Development of an in-vivo active reversible butyrylcholinesterase inhibitor.
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- Scientific Reports, 2016, p. 39495, doi. 10.1038/srep39495
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Structural analysis of point mutations at the Vaccinia virus A20/D4 interface.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2016, v. 72, n. 9, p. 687, doi. 10.1107/S2053230X16011778
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Three conserved histidine residues contribute to mitochondrial iron transport through mitoferrins.
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- Biochemical Journal, 2014, v. 460, n. 1, p. 79, doi. 10.1042/BJ20140107
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Crystal Structure of the Vaccinia Virus DNA Polymerase Holoenzyme Subunit D4 in Complex with the A20 N-Terminal Domain.
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- PLoS Pathogens, 2014, v. 10, n. 3, p. 1, doi. 10.1371/journal.ppat.1003978
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An EPR/HYSCORE, Mössbauer, and resonance Raman study of the hydrogenase maturation enzyme HydF: a model for N-coordination to [4Fe-4S] clusters.
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- Journal of Biological Inorganic Chemistry (JBIC), 2014, v. 19, n. 1, p. 75, doi. 10.1007/s00775-013-1062-9
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Human butyrylcholinesterase produced in insect cells: huprine-based affinity purification and crystal structure.
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- FEBS Journal, 2012, v. 279, n. 16, p. 2905, doi. 10.1111/j.1742-4658.2012.08672.x
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Biochemical characterization of the HydE and HydG iron-only hydrogenase maturation enzymes from Thermatoga maritima
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- FEBS Letters, 2005, v. 579, n. 22, p. 5055, doi. 10.1016/j.febslet.2005.07.092
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Genetic ablations of iron regulatory proteins 1 and 2 reveal why iron regulatory protein 2 dominates iron homeostastis.
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- EMBO Journal, 2004, v. 23, n. 2, p. 386, doi. 10.1038/sj.emboj.7600041
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