Clark Sehon

Affiliations: 
1997 University of Virginia, Charlottesville, VA 
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"Clark Sehon"
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Harris PA, Faucher N, George N, et al. (2019) Discovery and Lead-optimization of 4,5-Dihydropyrazoles as Mono-Kinase Selective, Orally Bioavailable and Efficacious Inhibitors of Receptor Interacting Protein 1 (RIP1) Kinase. Journal of Medicinal Chemistry
Harris PA, Berger SB, Jeong JU, et al. (2017) Discovery of a First-in-Class Receptor Interacting Protein 1 (RIP1) Kinase Specific Clinical Candidate (GSK2982772) for the Treatment of Inflammatory Diseases. Journal of Medicinal Chemistry
Mandal P, Berger SB, Pillay S, et al. (2014) RIP3 induces apoptosis independent of pronecrotic kinase activity. Molecular Cell. 56: 481-95
Rickard DJ, Sehon CA, Kasparcova V, et al. (2014) Identification of selective small molecule inhibitors of the nucleotide-binding oligomerization domain 1 (NOD1) signaling pathway. Plos One. 9: e96737
Kaiser WJ, Sridharan H, Huang C, et al. (2013) Toll-like receptor 3-mediated necrosis via TRIF, RIP3, and MLKL. The Journal of Biological Chemistry. 288: 31268-79
Rickard DJ, Sehon CA, Kasparcova V, et al. (2013) Identification of benzimidazole diamides as selective inhibitors of the nucleotide-binding oligomerization domain 2 (NOD2) signaling pathway. Plos One. 8: e69619
Gatheral T, Reed DM, Moreno L, et al. (2012) A key role for the endothelium in NOD1 mediated vascular inflammation: comparison to TLR4 responses. Plos One. 7: e42386
Wang GZ, Haile PA, Daniel T, et al. (2011) CCR2 receptor antagonists: optimization of biaryl sulfonamides to increase activity in whole blood. Bioorganic & Medicinal Chemistry Letters. 21: 7291-4
Mapes CM, Mani NS, Deng X, et al. (2010) Practical and scalable synthesis of a selective CCK1 receptor antagonist. The Journal of Organic Chemistry. 75: 7950-3
Behm DJ, Aiyar NV, Olzinski AR, et al. (2010) GSK1562590, a slowly dissociating urotensin-II receptor antagonist, exhibits prolonged pharmacodynamic activity ex vivo. British Journal of Pharmacology. 161: 207-28
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