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An Oral Sphingosine 1‑Phosphate Receptor 1 (S1P1) Antagonist Prodrug with Efficacy in Vivo: Discovery, Synthesis, and Evaluation
American Chemical Society | 2012| -
An Oral Sphingosine 1-Phosphate Receptor 1 (S1P1) Antagonist Prodrug with Efficacy in Vivo: Discovery, Synthesis, and Evaluation
Online Contents | 2012|Contributors: Janser, Philipp -
A Potent and Selective S1P1 Antagonist with Efficacy in Experimental Autoimmune Encephalomyelitis
Online Contents | 2012|Contributors: Janser, Philipp -
Design and preparation of 2-benzamido-pyrimidines as inhibitors of IKK
Online Contents | 2006|Contributors: Janser, Philipp -
Design of Potent and Selective Covalent Inhibitors of Bruton’s Tyrosine Kinase Targeting an Inactive Conformation
American Chemical Society | 2019| -
Discovery of LOU064 (Remibrutinib), a Potent and Highly Selective Covalent Inhibitor of Bruton’s Tyrosine Kinase
American Chemical Society | 2020| -
Discovery of Potent, Orally Bioavailable, Tricyclic NLRP3 Inhibitors
American Chemical Society | 2024| -
Gold and silver hydrides: synthesis of heterobimetallic iridium-M (M = gold, silver) complexes and x-ray crystal structures of [(PPh3)Au(.mu.-H)IrH2(PPh3)3](BF4) and [(PPh3)Ag(.mu.-H)IrH2(PPh3)3](CF3SO3)
National licenceAmerican Chemical Society | 1989| -
Highly diastereoselective Lewis acid promoted Claisen-Ireland rearrangement
Online Contents | 2002|Contributors: Janser, Philipp
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