Daniel Rauh
Affiliations: | 2003-2005 | Cellular and Molecular Pharmacology | University of California, San Francisco, San Francisco, CA |
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"Daniel Rauh"
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Publications
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Schulz T, Gontla R, Teuber A, et al. (2025) Design, Synthesis, and SAR of Covalent KIT and PDGFRA Inhibitors─Exploring Their Potential in Targeting GIST. Journal of Medicinal Chemistry |
Pervanidis KA, D'Angelo GD, Weisner J, et al. (2024) Akt Inhibitor Advancements: From Capivasertib Approval to Covalent-Allosteric Promises. Journal of Medicinal Chemistry. 67: 6052-6063 |
Grabe T, Jeyakumar K, Niggenaber J, et al. (2023) Addressing the Osimertinib Resistance Mutation EGFR-L858R/C797S with Reversible Aminopyrimidines. Acs Medicinal Chemistry Letters. 14: 591-598 |
Goebel L, Kirschner T, Koska S, et al. (2023) Targeting oncogenic KRasG13C with nucleotide-based covalent inhibitors. Elife. 12 |
Stehle J, Weisner J, Eichhorn L, et al. (2023) Insights into the Conformational Plasticity of the Protein Kinase Akt1 by Multi-Lateral Dipolar Spectroscopy. Chemistry (Weinheim An Der Bergstrasse, Germany). e202203959 |
Gehrtz P, Marom S, Bührmann M, et al. (2022) Optimization of Covalent MKK7 Inhibitors Crude Nanomole-Scale Libraries. Journal of Medicinal Chemistry |
Lategahn J, Tumbrink HL, Schultz-Fademrecht C, et al. (2022) Insight into Targeting Exon20 Insertion Mutations of the Epidermal Growth Factor Receptor with Wild Type-Sparing Inhibitors. Journal of Medicinal Chemistry |
van der Westhuizen L, Weisner J, Taher A, et al. (2022) Covalent allosteric inhibitors of Akt generated using a click fragment approach. Chemmedchem |
Quambusch L, Depta L, Landel I, et al. (2021) Cellular model system to dissect the isoform-selectivity of Akt inhibitors. Nature Communications. 12: 5297 |
Niggenaber J, Heyden L, Grabe T, et al. (2020) Complex Crystal Structures of EGFR with Third-Generation Kinase Inhibitors and Simultaneously Bound Allosteric Ligands. Acs Medicinal Chemistry Letters. 11: 2484-2490 |