Hannelore Stockhausen
Grünenthal Group (Germany)(DE)
Publications by Year
Research Areas
Ion Channels and Receptors, Pain Mechanisms and Treatments, Phytochemicals and Antioxidant Activities, Ion channel regulation and function, Biochemical Analysis and Sensing Techniques
Most-Cited Works
- → Reduction of myocardial reperfusion injury by an inhibitor of poly (ADP-ribose) synthetase in the pig(1998)46 cited
- → 2-(3-Fluoro-4-methylsulfonylaminophenyl)propanamides as Potent Transient Receptor Potential Vanilloid 1 (TRPV1) Antagonists: Structure–Activity Relationships of 2-Amino Derivatives in theN-(6-Trifluoromethylpyridin-3-ylmethyl) C-Region(2012)40 cited
- → Inhibition by N‐acetyl‐5‐hydroxytryptamine of nitric oxide synthase expression in cultured cells and in the anaesthetized rat(1995)28 cited
- → Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists(2017)21 cited
- → In vitro characterization of the thermoneutral transient receptor potential vanilloid-1 (TRPV1) inhibitor GRTE16523(2020)17 cited
- → Pyridine C-region analogs of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists(2015)15 cited
- → 2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists(2014)14 cited
- → Discovery of indane propanamides as potent and selective TRPV1 antagonists(2019)14 cited
- → Discovery of 1-(1H-indazol-4-yl)-3-((1-phenyl-1H-pyrazol-5-yl)methyl) ureas as potent and thermoneutral TRPV1 antagonists(2020)11 cited
- → α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists(2015)11 cited