Martin Neuenschwander

Berlin, BE, Germany

Last Updated: 09/26/2026

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Found 48 publications

Novel Deiodinase 2-Selective Inhibitors-Possible Reference Substances for Regulatory In Vitro Tests for Endocrine Disruptors and Drugs Targeting T3-Dependent Processes.

Novel Deiodinase 2-Selective Inhibitors-Possible Reference Substances for Regulatory In Vitro Tests for Endocrine Disruptors and Drugs Targeting T3-Dependent Processes.

Journal: Thyroid : official journal of the American Thyroid Association
Published: March 13, 2026

Discovery and characterization of a novel class of cyclic peptidic compounds inhibiting the subunit interaction of the protein kinase CK2α2β2 holoenzyme.

Discovery and characterization of a novel class of cyclic peptidic compounds inhibiting the subunit interaction of the protein kinase CK2α2β2 holoenzyme.

Journal: RSC chemical biology
Published: March 12, 2026

DFT guided design of novel quinone bioisosteres as inhibitors of the clathrin N-terminal domain-amphiphysin protein-protein interaction. Dihydroquinazolin-4(1H)-ones and quinazolin-3(4H)-ones.

DFT guided design of novel quinone bioisosteres as inhibitors of the clathrin N-terminal domain-amphiphysin protein-protein interaction. Dihydroquinazolin-4(1H)-ones and quinazolin-3(4H)-ones.

Journal: European journal of medicinal chemistry
Published: January 15, 2026

Cell Painting Protocol to Characterize Morphological Profiles of Large Compound Collections Using the EU-OPENSCREEN Library.

Cell Painting Protocol to Characterize Morphological Profiles of Large Compound Collections Using the EU-OPENSCREEN Library.

Journal: Methods in molecular biology (Clifton, N.J.)
Published: January 01, 2026

Targeting the Membrane-Embedded Rhomboid Protease GlpG: A Multimodal Strategy for Inhibitor Discovery and Mechanistic Insight.

Targeting the Membrane-Embedded Rhomboid Protease GlpG: A Multimodal Strategy for Inhibitor Discovery and Mechanistic Insight.

Journal: Angewandte Chemie (International ed. in English)
Published: June 27, 2025

Inhibition of the Clathrin Terminal Domain-Amphiphysin Protein-Protein Interaction. Probing the Pitstop 2 Aromatic Moiety.

Inhibition of the Clathrin Terminal Domain-Amphiphysin Protein-Protein Interaction. Probing the Pitstop 2 Aromatic Moiety.

Journal: ChemMedChem
Published: April 27, 2025

Identification and Characterization of Highly Potent and Isoenzyme-Selective Inhibitors of Deiodinase Type I via a Nonradioactive High-Throughput Screening Method.

Identification and Characterization of Highly Potent and Isoenzyme-Selective Inhibitors of Deiodinase Type I via a Nonradioactive High-Throughput Screening Method.

Journal: Thyroid : official journal of the American Thyroid Association
Published: April 02, 2025

Morphological profiling data resource enables prediction of chemical compound properties.

Morphological profiling data resource enables prediction of chemical compound properties.

Journal: iScience
Published: October 07, 2024

7,8-Dihydroxyflavone is a direct inhibitor of human and murine pyridoxal phosphatase.

7,8-Dihydroxyflavone is a direct inhibitor of human and murine pyridoxal phosphatase.

Journal: eLife
Published: June 10, 2024

Identification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4.

Identification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4.

Journal: PloS one
Published: April 09, 2024

An unconventional gatekeeper mutation sensitizes inositol hexakisphosphate kinases to an allosteric inhibitor.

An unconventional gatekeeper mutation sensitizes inositol hexakisphosphate kinases to an allosteric inhibitor.

Journal: eLife
Published: October 16, 2023

Structural Basis for Highly Selective Class II Alpha Phosphoinositide-3-Kinase Inhibition.

Structural Basis for Highly Selective Class II Alpha Phosphoinositide-3-Kinase Inhibition.

Journal: Journal of medicinal chemistry
Published: October 11, 2023
Showing 1-12 of 48

Last Updated: 09/26/2026