PMID

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Direct targeting ofß-catenin: Inhibition of protein-protein interactions for the inactivation of Wnt signaling.

Chemical Genomics Centre of The Max Planck Society

Structure-based design, synthesis and biological evaluation of N-pyrazole, N'-thiazole urea inhibitors of MAP kinase p38a.

Chemical Genomics Centre of The Max Planck Society

Synthesis and biological evaluation of 7-substituted-1-(3-bromophenylamino)isoquinoline-4-carbonitriles as inhibitors of myosin light chain kinase and epidermal growth factor receptor.

Chemical Genomics Centre of The Max Planck Society

Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor.

Chemical Genomics Centre of The Max Planck Society

Displacement assay for the detection of stabilizers of inactive kinase conformations.

Chemical Genomics Centre of The Max Planck Society

Structure-Based Design of Non-natural Macrocyclic Peptides That Inhibit Protein-Protein Interactions.

Chemical Genomics Centre of The Max Planck Society

2-pyridyloxy-4-ether orexin receptor antagonists

Merck Sharp & Dohme

Design of Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase with Improved Drug Resistance Properties. 1.

University of Oxford

Structural Insight into the Stereoselective Inhibition of MMP-8 by Enantiomeric Sulfonamide Phosphonates.

Istituto Di Cristallografia