Paul Erdman
AbbVie (United States)(US)BioTheryX (United States)(US)
Publications by Year
Research Areas
Cytokine Signaling Pathways and Interactions, Synthesis and biological activity, Protein Degradation and Inhibitors, Multiple Myeloma Research and Treatments, NF-κB Signaling Pathways
Most-Cited Works
- → Small Molecules Co-targeting CKIα and the Transcriptional Kinases CDK7/9 Control AML in Preclinical Models(2018)148 cited
- → Discovery of Antibacterial Biotin Carboxylase Inhibitors by Virtual Screening and Fragment-Based Approaches(2009)105 cited
- → Inhibitors of NF-κB and AP-1 Gene Expression: SAR Studies on the Pyrimidine Portion of 2-Chloro-4-trifluoromethylpyrimidine-5-[N-(3‘,5‘-bis(trifluoromethyl)phenyl)carboxamide](2000)80 cited
- → The Discovery of a Dual TTK Protein Kinase/CDC2-Like Kinase (CLK2) Inhibitor for the Treatment of Triple Negative Breast Cancer Initiated from a Phenotypic Screen(2017)59 cited
- → Structure–Activity Relationship Studies of Ethyl 2-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-4-(trifluoromethyl)pyrimidine-5-carboxylate: An Inhibitor of AP-1 and NF-κB Mediated Gene Expression(2002)45 cited
- → 2-Chloro-4-(trifluoromethyl)pyrimidine-5-N-(3‘,5‘-bis(trifluoromethyl)phenyl)- carboxamide: A Potent Inhibitor of NF-κB- and AP-1-Mediated Gene Expression Identified Using Solution-Phase Combinatorial Chemistry(1998)44 cited
- → The design and synthesis of novel orally active inhibitors of AP-1 and NF-κB mediated transcriptional activation. SAR of In vitro and In vivo studies(2003)41 cited
- → Discovery of the c-Jun N-Terminal Kinase Inhibitor CC-90001(2021)37 cited
- → Design and Synthesis of Pyrrolidine-based Fragments That Sample Three-dimensional Molecular Space(2019)33 cited
- → Novel inhibitors of AP-1 and NF-κB mediated gene expression: structure–activity relationship studies of ethyl 4-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate(2000)31 cited