Patrick Eidam
Affiliations: | 2001-2006 | Chemistry | University of Virginia, Charlottesville, VA |
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"Patrick Eidam"Mean distance: 8.62 | S | N | B | C | P |
Parents
Sign in to add mentor| James A. Marshall | grad student | 2001-2006 | UVA | |
| (The formal synthesis of ( - )-callipeltoside A and related studies) | ||||
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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 |
| 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 |
| 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 |
| Morales-Ramos ÃI, Li YH, Hilfiker M, et al. (2011) Structure-activity relationship studies of novel 3-oxazolidinedione-6-naphthyl-2-pyridinones as potent and orally bioavailable EP3 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 21: 2806-11 |
| Jin J, Morales-Ramos A, Eidam P, et al. (2010) Novel 3-Oxazolidinedione-6-aryl-pyridinones as Potent, Selective, and Orally Active EP3 Receptor Antagonists. Acs Medicinal Chemistry Letters. 1: 316-20 |
| Marshall JA, Eidam PM. (2008) A formal synthesis of the callipeltoside aglycone. Organic Letters. 10: 93-6 |
| Marshall J, Herold M, Eidam H, et al. (2007) Pd- and Cu-Catalyzed 1,4-Addition of Dialkylzinc Compounds to α,β-Enals Synfacts. 2007: 0197-0197 |
| Marshall JA, Eidam P, Eidam HS. (2007) Synthesis of 4‐Triisopropylsilyl‐3‐Butyn‐2‐ol by Asymmetric Transfer Hydrogenation Organic Syntheses. 120-128 |
| Marshall JA, Eidam P, Eidam HS. (2007) Synthesis of 4-triisopropylsilyl-3-butyn-2-ol by asymmetric transfer hydrogenation Organic Syntheses. 84: 120-128 |