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Norbert Furtmann

University of Bonn

36

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527

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An end-to-end automated platform process for high-throughput engineering of next-generation multi-specific antibody therapeutics.

2021 mAbs
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Identification of New Chromenone Derivatives as Cholinesterase Inhibitors and Molecular Docking Studies

2018 Medicinal Chemistry
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Chalcone Isomerase from Eubacterium ramulus Catalyzes the Ring Contraction of Flavanonols

2016 Journal of Bacteriology
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En Route to New Therapeutic Options for Iron Overload Diseases: Matriptase-2 as a Target for Kunitz-Type Inhibitors.

2016 ChemBioChem
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Coumarin-thiazole and -oxadiazole derivatives: Synthesis, bioactivity and docking studies for aldose/aldehyde reductase inhibitors

2016 Bioorganic Chemistry
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Back Cover: Phosphono Bisbenzguanidines as Irreversible Dipeptidomimetic Inhibitors and Activity‐Based Probes of Matriptase‐2 (Chem. Eur. J. 25/2016)

2016 Chemistry: A European Journal
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Limiting the Number of Potential Binding Modes by Introducing Symmetry into Ligands: Structure‐Based Design of Inhibitors for Trypsin‐Like Serine Proteases

2016 Chemistry: A European Journal
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Cover Picture: En Route to New Therapeutic Options for Iron Overload Diseases: Matriptase‐2 as a Target for Kunitz‐Type Inhibitors (ChemBioChem 7/2016)

2016 ChemBioChem
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Phosphono Bisbenzguanidines as Irreversible Dipeptidomimetic Inhibitors and Activity‐Based Probes of Matriptase‐2

2016 Chemistry: A European Journal
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Oxidation of Disulfides to Taurine and Sulfanilic Acid Derivatives

2015 Synthesis
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