M. Kohlmann

发表

Targeting DnaN for tuberculosis therapy using novel griselimycins

H. Matter, D. Heinz, R. Müller, 2015, Science.

Discovery and pharmacological characterization of SAR707 as novel and selective small molecule inhibitor of stearoyl-CoA desaturase (SCD1).

H. Matter, A. Herling, S. Keil, 2013, European journal of pharmacology.

Differential epitope identification of antibodies against intracellular domains of alzheimer's amyloid precursor protein using high resolution affinity-mass spectrometry.

M. Przybylski, Madalina Maftei, M. Kohlmann, 2007, Sub-cellular biochemistry.

Pharmacological Characterization of SAR407899, a Novel Rho-Kinase Inhibitor

A. Kannt, J. Herbert, H. Ruetten, 2009, Hypertension.

Mechanistic investigations of the liver toxicity of the free fatty acid receptor 1 agonist fasiglifam (TAK875) and its primary metabolites

Friedemann Schmidt, A. Dudda, D. Weitz, 2019, Journal of biochemical and molecular toxicology.

Identification and characterisation of carnostatine (SAN9812), a potent and selective carnosinase (CN1) inhibitor with in vivo activity

H. Hammes, M. Teufel, T. Albrecht, 2018, Diabetologie und Stoffwechsel.

End-organ protection in hypertension by the novel and selective Rho-kinase inhibitor, SAR407899.

A. Kannt, H. Ruetten, A. Schiffer, 2015, World journal of cardiology.

Novel Small Molecule Inhibitors of Activated Thrombin Activatable Fibrinolysis Inhibitor (TAFIa) from Natural Product Anabaenopeptin.

A. Evers, H. Schreuder, M. Kurz, 2015, Journal of medicinal chemistry.

Amphetamine and methamphetamine determination in urine by reversed-phase high-performance liquid chromatography with simultaneous sample clean-up and derivatization with 1,2-naphthoquinone 4-sulphonate on solid-phase cartridges.

P. Campíns-Falcó, C. Molins-Legua, M. Kohlmann, 1996, Journal of chromatography. B, Biomedical applications.

Identification of high-affinity P2Y₁₂ antagonists based on a phenylpyrazole glutamic acid piperazine backbone.

G. Hessler, A. Evers, Tilo Weiss, 2012, Journal of medicinal chemistry.

Identification and Structural Characterisation of Carboxy-Terminal Polypeptides and Antibody Epitopes of Alzheimer's Amyloid Precursor Protein Using High-Resolution Mass Spectrometry

P. S. St George-Hyslop, M. Ehrmann, J. McLaurin, 2005, European journal of mass spectrometry.

Small Macrocycles As Highly Active Integrin α2β1 Antagonists.

Christian Buning, C. Buning, M. Kohlmann, 2014, ACS medicinal chemistry letters.

"Affinity-proteomics": direct protein identification from biological material using mass spectrometric epitope mapping

S. Deininger, Eugen Damoc, M. Przybylski, 2004, Analytical and bioanalytical chemistry.

Additive efficacy of a bispecific anti–TNF/IL-6 nanobody compound in translational models of rheumatoid arthritis

M. Herrmann, Virginia Savova, F. Nestle, 2023, Science Translational Medicine.

Novel β-amino acid derivatives as inhibitors of cathepsin A.

C. Buning, G. Horstick, H. Schreuder, 2012, Journal of medicinal chemistry.

23. The Discovery of Cathepsin A Inhibitors: A Project-Adapted Fragment Approach Based on HTS Results

C. Buning, G. Horstick, H. Schreuder, 2016 .

Characterization of Non-Covalent Complexes of Synthetic Peptides of RNA Polymerase Subunit σ70 From Chlamydia trachomatis with Protein G by nanoESI-MS

Shuying Liu, Li Ma, M. Przybylski, 2015 .

An orally available small molecule that targets soluble TNF to deliver anti-TNF biologic-like efficacy in rheumatoid arthritis

M. Herrmann, Helen T Horsley, D. Weitz, 2022, Frontiers in Pharmacology.

Mass Spectrometric Analysis of Noncovalent Complexes Between Synthetic Peptides from Human Ribosomal Protein L7 and Protein G

U. Krawinkel, Shuying Liu, Li Ma, 2015 .

Absorption – in-vitro Tests – Non-Cell Based

M. Kohlmann, 2006 .

Benzimidazole-carboxamides as potent and bioavailable stearoyl-CoA desaturase (SCD1) inhibitors from ligand-based virtual screening and chemical optimization.

H. Matter, A. Herling, J. Sánchez-Arias, 2013, Bioorganic & medicinal chemistry letters.

Sulfamide as Zinc Binding Motif in Small Molecule Inhibitors of Activated Thrombin Activatable Fibrinolysis Inhibitor (TAFIa).

A. Evers, H. Schreuder, M. Follmann, 2016, Journal of medicinal chemistry.

Spectrophotometric assay for amidolytic activity of alkaline protease from Pseudomonas aeruginosa

J. Wallach, M. Kohlmann, D. Louis, 1997 .

Small Macrocycles As Highly Active Integrin α2β1 Antagonists.

C. Buning, M. Kohlmann, N. Halland, 2014, ACS medicinal chemistry letters.