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Development of an in-vivo active reversible butyrylcholinesterase inhibitor

Scientific reports, 2016-12, Vol.6 (1), p.39495-39495, Article 39495

2016

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Synthesis and Biochemical Evaluation of Warhead-Decorated Psoralens as (Immuno)Proteasome Inhibitors

Molecules (Basel, Switzerland), 2021-01, Vol.26 (2), p.356

2021

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Glycosaminoglycans as Tools to Decipher the Platelet Tumor Cell Interaction: A Focus on P-Selectin

Molecules (Basel, Switzerland), 2020-02, Vol.25 (5), p.1039

2020

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Assessment of Tractable Cysteines for Covalent Targeting by Screening Covalent Fragments

Chembiochem : a European journal of chemical biology, 2021-02, Vol.22 (4), p.743-753

2021

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Nonpeptidic Selective Inhibitors of the Chymotrypsin-Like (β5 i) Subunit of the Immunoproteasome

Angewandte Chemie International Edition, 2016-05, Vol.55 (19), p.5745-5748

International ed. in English, 2016

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Design and synthesis of amino-substituted N-arylpiperidinyl-based inhibitors of the (immuno)proteasome

Acta Pharmaceutica, 2023-09, Vol.73 (3), p.441-456

2023

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Inhibition of O-GlcNAc Transferase Alters the Differentiation and Maturation Process of Human Monocyte Derived Dendritic Cells

Cells (Basel, Switzerland), 2021-11, Vol.10 (12), p.3312

2021

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Editorial: The Role of Platelets in Cancer Progression and Malignancy

Frontiers in oncology, 2021-12, Vol.11, p.814006-814006

2021

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Discovery of Immunoproteasome Inhibitors Using Large-Scale Covalent Virtual Screening

Molecules (Basel, Switzerland), 2019-07, Vol.24 (14), p.2590

2019

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Intracellular Hydrolysis of Small-Molecule O -Linked N -Acetylglucosamine Transferase Inhibitors Differs among Cells and Is Not Required for Its Inhibition

Molecules (Basel, Switzerland), 2020-07, Vol.25 (15), p.3381

2020

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Structure-Activity Relationships of Benzothiazole-Based Hsp90 C-Terminal-Domain Inhibitors

Pharmaceutics, 2021-08, Vol.13 (8), p.1283

2021

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In Silico Discovery and Optimisation of a Novel Structural Class of Hsp90 C-Terminal Domain Inhibitors

Biomolecules (Basel, Switzerland), 2022-06, Vol.12 (7), p.884

2022

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Discovery of a New Drug-like Series of OGT Inhibitors by Virtual Screening

Molecules (Basel, Switzerland), 2022-03, Vol.27 (6), p.1996

2022

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Selective cytotoxicity of amidinopiperidine based compounds towards Burkitt's lymphoma cells involves proteasome inhibition

PloS one, 2012-07, Vol.7 (7), p.e41961-e41961

2012

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Fragment-Sized and Bidentate (Immuno)Proteasome Inhibitors Derived from Cysteine and Threonine Targeting Warheads

Cells (Basel, Switzerland), 2021-12, Vol.10 (12), p.3431

2021

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New Quinolinone O-GlcNAc Transferase Inhibitors Based on Fragment Growth

Frontiers in chemistry, 2021-04, Vol.9, p.666122-666122

2021

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Halogenation of common phenolic household and personal care product ingredients enhances their AhR-modulating capacity

Chemosphere (Oxford), 2024-02, Vol.350, p.141116-141116, Article 141116

2024

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Modulating Immune Responses: The Double-Edged Sword of Platelet CD40L

Seminars in thrombosis and hemostasis, 2024-10

2024

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Discovery of novel small-molecule compounds with selective cytotoxicity for Burkitt's lymphoma cells using 3D ligand-based virtual screening

Molecules (Basel, Switzerland), 2014-11, Vol.19 (11), p.19209-19219

2014

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Halogenated ingredients of household and personal care products as emerging endocrine disruptors

Chemosphere (Oxford), 2022-09, Vol.303 (Pt 1), p.134824-134824, Article 134824

2022

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In vitro investigation of immunomodulatory activities of selected UV-filters

Food and chemical toxicology, 2023-04, Vol.174, p.113684-113684, Article 113684

2023

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Environmental contamination status with common ingredients of household and personal care products exhibiting endocrine-disrupting potential

Environmental science and pollution research international, 2022-10, Vol.29 (49), p.73648-73674

2022

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Structural characterization and biological evaluation of a clioquinol-ruthenium complex with copper-independent antileukaemic activity

Dalton transactions : an international journal of inorganic chemistry, 2014-06, Vol.43 (24), p.9045-9051

2014

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Targeting the deubiquitinase USP7 for degradation with PROTACs

Chemical communications (Cambridge, England), 2022-08, Vol.58 (63), p.8858-8861

2022

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Optimisation of pyrazolo[1,5-a]pyrimidin-7(4H)-one derivatives as novel Hsp90 C-terminal domain inhibitors against Ewing sarcoma

Bioorganic chemistry, 2023-02, Vol.131, p.106311-106311, Article 106311

2023

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Development of an in-vivo active reversible butyrylcholinesterase inhibitor

Synthesis and Biochemical Evaluation of Warhead-Decorated Psoralens as (Immuno)Proteasome Inhibitors

Glycosaminoglycans as Tools to Decipher the Platelet Tumor Cell Interaction: A Focus on P-Selectin

Assessment of Tractable Cysteines for Covalent Targeting by Screening Covalent Fragments

Nonpeptidic Selective Inhibitors of the Chymotrypsin-Like (β5 i) Subunit of the Immunoproteasome

Design and synthesis of amino-substituted N-arylpiperidinyl-based inhibitors of the (immuno)proteasome

Inhibition of O-GlcNAc Transferase Alters the Differentiation and Maturation Process of Human Monocyte Derived Dendritic Cells

Editorial: The Role of Platelets in Cancer Progression and Malignancy

Discovery of Immunoproteasome Inhibitors Using Large-Scale Covalent Virtual Screening

Intracellular Hydrolysis of Small-Molecule O -Linked N -Acetylglucosamine Transferase Inhibitors Differs among Cells and Is Not Required for Its Inhibition

Structure-Activity Relationships of Benzothiazole-Based Hsp90 C-Terminal-Domain Inhibitors

In Silico Discovery and Optimisation of a Novel Structural Class of Hsp90 C-Terminal Domain Inhibitors

Discovery of a New Drug-like Series of OGT Inhibitors by Virtual Screening

Selective cytotoxicity of amidinopiperidine based compounds towards Burkitt's lymphoma cells involves proteasome inhibition

Fragment-Sized and Bidentate (Immuno)Proteasome Inhibitors Derived from Cysteine and Threonine Targeting Warheads

New Quinolinone O-GlcNAc Transferase Inhibitors Based on Fragment Growth

Halogenation of common phenolic household and personal care product ingredients enhances their AhR-modulating capacity

Modulating Immune Responses: The Double-Edged Sword of Platelet CD40L

Discovery of novel small-molecule compounds with selective cytotoxicity for Burkitt's lymphoma cells using 3D ligand-based virtual screening

Halogenated ingredients of household and personal care products as emerging endocrine disruptors

In vitro investigation of immunomodulatory activities of selected UV-filters

Environmental contamination status with common ingredients of household and personal care products exhibiting endocrine-disrupting potential

Structural characterization and biological evaluation of a clioquinol-ruthenium complex with copper-independent antileukaemic activity

Targeting the deubiquitinase USP7 for degradation with PROTACs

Optimisation of pyrazolo[1,5-a]pyrimidin-7(4H)-one derivatives as novel Hsp90 C-terminal domain inhibitors against Ewing sarcoma

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