Publications of Daniel Rauh
All genres
Journal Article (50)
Journal Article
17 (11), pp. 990 - 994 (2016)
Monitoring Conformational Changes in the Receptor Tyrosine Kinase EGFR. ChemBioChem: A European Journal of Chemical Biology
Journal Article
10 (1), pp. 279 - 288 (2015)
Discovery of Inter-Domain Stabilizers-A Novel Assay System for Allosteric Akt Inhibitors. ACS Chemical Biology
Journal Article
57 (10), pp. 4252 - 4262 (2014)
Identification of Type II and III DDR2 Inhibitors. Journal of Medicinal Chemistry
Journal Article
56 (14), 1, pp. 5757 - 5772 (2013)
Targeting Gain of Function and Resistance Mutations in Abl and KIT by Hybrid Compound Design. Journal of Medicinal Chemistry
Journal Article
135 (22), 1, pp. 8400 - 8408 (2013)
Overcoming Compound Fluorescence in the FLiK Screening Assay with Red-Shifted Fluorophores. Journal of the American Chemical Society
Journal Article
135 (18), 1, pp. 6838 - 6841 (2013)
Selective Detection of Allosteric Phosphatase Inhibitors. Journal of the American Chemical Society
Journal Article
5 (1), 1, pp. 21 - 28 (2013)
Natural-product-derived fragments for fragment-based ligand discovery. Nature Chemistry
Journal Article
109 (42), 1, pp. 17034 - 17039 (2012)
A framework for identification of actionable cancer genome dependencies in small cell lung cancer. Proceedings of the National Academy of Sciences of the United States of America
Journal Article
7 (7), 1, pp. e39713-1 - e39713-10 (2012)
Fluorophore Labeled Kinase Detects Ligands That Bind within the MAPK Insert of p38α Kinase. PLoS ONE
Journal Article
134 (22), 1, pp. 9138 - 9141 (2012)
Direct Binding Assay for the Detection of Type IV Allosteric Inhibitors of Abl. Journal of the American Chemical Society
Journal Article
7 (7), 1, pp. 1257 - 1267 (2012)
Targeting GSK3 from Ustilago maydis: Type-II Kinase Inhibitors as Potential Antifungals. ACS Chemical Biology
Journal Article
7 (4), 1, pp. 723 - 731 (2012)
A Chemical Genetic Approach for Covalent Inhibition of Analogue-Sensitive Aurora Kinase. ACS Chemical Biology
Journal Article
67 (52), 1, pp. 10195 - 10202 (2011)
Enantioselective synthesis of the spirotryprostatin A scaffold. Tetrahedron
Journal Article
67 (35), 1, pp. 6713 - 6729 (2011)
Identification and further development of thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B. Tetrahedron
Journal Article
6 (9), 1, pp. 926 - 933 (2011)
Identification of Ustilago maydis Aurora Kinase As a Novel Antifungal Target. Asc Chemical Biology
Journal Article
19 (1), 1, pp. 429 - 439 (2011)
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. Bioorganic & Medicinal Chemistry
Journal Article
19 (7), 1, pp. 2145 - 2155 (2011)
Using small molecules to target protein phosphatases. Bioorganic & Medicinal Chemistry
Journal Article
11 (18), 1, pp. 2557 - 2566 (2010)
Characterization of Irreversible Kinase Inhibitors by Directly Detecting Covalent Bond Formation: A Tool for Dissecting Kinase Drug Resistance. ChemBioChem
Journal Article
11 (12), 1, pp. 1645 - 1648 (2010)
RAF Kinase Inhibitors in Cancer Treatment: Like a Bull in a China Shop? ChemBioChem
Journal Article
122 (34), 1, pp. 6038 - 6041 (2010)
Identification of Thiazolidinones Spiro-Fused to Indolin-2-ones as Potent and Selective Inhibitors of the Mycobacterium tuberculosis Protein Tyrosine Phosphatase B. Angewandte Chemie