Stephan Röver

Synthesis and Biochemical Evaluation of<i>N</i>-(4-Phenylthiazol-2-yl)benzenesulfonamides as High-Affinity Inhibitors of Kynurenine 3-Hydroxylase

Stephan Röver, Andrea M. Cesura, Philipp Huguenin et al. · Journal of Medicinal Chemistry · 1997 · 208 citations · Full text

Medicinal Chemistry, Pharmacological Study, Biochemistry +14

High-Affinity, Non-Peptide Agonists for the ORL1 (Orphanin FQ/Nociceptin) Receptor

Stephan Röver, Geo Adam, Andrea M. Cesura et al. · Journal of Medicinal Chemistry · 2000 · 82 citations · Full text

Drug Target, Pain Medicine, Immunology +18

Synthesis and applications of fluorous silyl protecting groups with improved acid stability

Stephan Röver, Peter Wipf · Tetrahedron Letters · 1999 · 68 citations

Chemical Engineering, Engineering, Improved Acid Stability +4

8-Acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonists

J. Wichmann, Geo Adam, Stephan Röver et al. · Bioorganic & Medicinal Chemistry Letters · 1999 · 61 citations · Full text

Functional Selectivity, Medicine, Mechanism Of Action +4

Novel Triazolopyrimidine‐Derived Cannabinoid Receptor 2 Agonists as Potential Treatment for Inflammatory Kidney Diseases

Matthias Nettekoven, Jean‐Michel Adam, Stefanie Bendels et al. · ChemMedChem · 2015 · 56 citations

Renal Inflammation, Pharmacotherapy, Cannabinoid Pharmacology +20