Publikationen von Daniel Rauh
Alle Typen
Zeitschriftenartikel (50)
1.
Zeitschriftenartikel
17 (11), S. 990 - 994 (2016)
Monitoring Conformational Changes in the Receptor Tyrosine Kinase EGFR. ChemBioChem: A European Journal of Chemical Biology 2.
Zeitschriftenartikel
10 (1), S. 279 - 288 (2015)
Discovery of Inter-Domain Stabilizers-A Novel Assay System for Allosteric Akt Inhibitors. ACS Chemical Biology 3.
Zeitschriftenartikel
57 (10), S. 4252 - 4262 (2014)
Identification of Type II and III DDR2 Inhibitors. Journal of Medicinal Chemistry 4.
Zeitschriftenartikel
56 (14), 1, S. 5757 - 5772 (2013)
Targeting Gain of Function and Resistance Mutations in Abl and KIT by Hybrid Compound Design. Journal of Medicinal Chemistry 5.
Zeitschriftenartikel
135 (22), 1, S. 8400 - 8408 (2013)
Overcoming Compound Fluorescence in the FLiK Screening Assay with Red-Shifted Fluorophores. Journal of the American Chemical Society 6.
Zeitschriftenartikel
135 (18), 1, S. 6838 - 6841 (2013)
Selective Detection of Allosteric Phosphatase Inhibitors. Journal of the American Chemical Society 7.
Zeitschriftenartikel
5 (1), 1, S. 21 - 28 (2013)
Natural-product-derived fragments for fragment-based ligand discovery. Nature Chemistry 8.
Zeitschriftenartikel
109 (42), 1, S. 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 9.
Zeitschriftenartikel
7 (7), 1, S. e39713-1 - e39713-10 (2012)
Fluorophore Labeled Kinase Detects Ligands That Bind within the MAPK Insert of p38α Kinase. PLoS ONE 10.
Zeitschriftenartikel
134 (22), 1, S. 9138 - 9141 (2012)
Direct Binding Assay for the Detection of Type IV Allosteric Inhibitors of Abl. Journal of the American Chemical Society 11.
Zeitschriftenartikel
7 (7), 1, S. 1257 - 1267 (2012)
Targeting GSK3 from Ustilago maydis: Type-II Kinase Inhibitors as Potential Antifungals. ACS Chemical Biology 12.
Zeitschriftenartikel
7 (4), 1, S. 723 - 731 (2012)
A Chemical Genetic Approach for Covalent Inhibition of Analogue-Sensitive Aurora Kinase. ACS Chemical Biology 13.
Zeitschriftenartikel
67 (52), 1, S. 10195 - 10202 (2011)
Enantioselective synthesis of the spirotryprostatin A scaffold. Tetrahedron 14.
Zeitschriftenartikel
67 (35), 1, S. 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 15.
Zeitschriftenartikel
6 (9), 1, S. 926 - 933 (2011)
Identification of Ustilago maydis Aurora Kinase As a Novel Antifungal Target. Asc Chemical Biology 16.
Zeitschriftenartikel
19 (1), 1, S. 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 17.
Zeitschriftenartikel
19 (7), 1, S. 2145 - 2155 (2011)
Using small molecules to target protein phosphatases. Bioorganic & Medicinal Chemistry 18.
Zeitschriftenartikel
11 (18), 1, S. 2557 - 2566 (2010)
Characterization of Irreversible Kinase Inhibitors by Directly Detecting Covalent Bond Formation: A Tool for Dissecting Kinase Drug Resistance. ChemBioChem 19.
Zeitschriftenartikel
11 (12), 1, S. 1645 - 1648 (2010)
RAF Kinase Inhibitors in Cancer Treatment: Like a Bull in a China Shop? ChemBioChem 20.
Zeitschriftenartikel
122 (34), 1, S. 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