User profiles for D. Felsing
Dennis FelsingMaterialize Verified email at felsing.org Cited by 161 |
Automating regression verification
… Dennis Felsing† dennis.felsing@student.kit.edu Sarah Grebing† sarah.grebing@kit.edu …
Hähnle, and D. Sands. A theorem proving approach to analysis of secure information flow. …
Hähnle, and D. Sands. A theorem proving approach to analysis of secure information flow. …
Advances in dopamine D1 receptor ligands for neurotherapeutics
The dopamine D1 receptor (D1R) is essential for neurotransmission in various brain pathways
where it modulates key functions including voluntary movement, memory, attention and …
where it modulates key functions including voluntary movement, memory, attention and …
An Orally Active Phenylaminotetralin-Chemotype Serotonin 5-HT7 and 5-HT1A Receptor Partial Agonist That Corrects Motor Stereotypy in Mouse Models
… Given the poor affinity of (+)-5-FPT at D 2 receptors and our observations that (+)-5-FPT (5.6
mg/kg) did not significantly decrease hyperlocomotion elicited by amphetamine or affect …
mg/kg) did not significantly decrease hyperlocomotion elicited by amphetamine or affect …
Maternal opioid exposure culminates in perturbed murine neurodevelopment and hyperactive phenotype in adolescence
CR Schlagal, TJ Dunn, P Xu, DE Felsing, CR Merritt… - Neuroscience, 2021 - Elsevier
Opioid use by women during pregnancy has risen dramatically since 2004, accompanied by
a striking increase in the prevalence of neonatal opioid withdrawal syndrome (NOWS) and …
a striking increase in the prevalence of neonatal opioid withdrawal syndrome (NOWS) and …
[HTML][HTML] Biophysical validation of serotonin 5-HT2A and 5-HT2C receptor interaction
DE Felsing, NC Anastasio, JM Miszkiel, SR Gilbertson… - PLoS …, 2018 - journals.plos.org
… ligand affinity, by statistically comparing receptor affinity values (K d ). Data from saturation
binding isotherms are presented as B MAX and K d values (mean ± SEM), as computed by …
binding isotherms are presented as B MAX and K d values (mean ± SEM), as computed by …
Synthesis and pharmacological evaluation of noncatechol G protein biased and unbiased dopamine D1 receptor agonists
P Wang, DE Felsing, H Chen, SR Raval… - ACS Medicinal …, 2019 - ACS Publications
Noncatechol heterocycles have recently been discovered as potent and selective G protein
biased dopamine 1 receptor (D1R) agonists with superior pharmacokinetic properties. To …
biased dopamine 1 receptor (D1R) agonists with superior pharmacokinetic properties. To …
Discovery of potent and brain-penetrant GPR52 agonist that suppresses psychostimulant behavior
P Wang, DE Felsing, H Chen, SJ Stutz… - Journal of medicinal …, 2020 - ACS Publications
The G protein-coupled receptor 52 (GPR52) is an orphan receptor that is selectively
expressed in the striatum and regulates various brain functions through activation of cAMP-…
expressed in the striatum and regulates various brain functions through activation of cAMP-…
A novel aminotetralin-type serotonin (5-HT) 2C receptor-specific agonist and 5-HT2A competitive antagonist/5-HT2B inverse agonist with preclinical efficacy for …
CE Canal, D Morgan, D Felsing, K Kondabolu… - … of Pharmacology and …, 2014 - ASPET
Development of 5-HT 2C agonists for treatment of neuropsychiatric disorders, including
psychoses, substance abuse, and obesity, has been fraught with difficulties, because the vast …
psychoses, substance abuse, and obesity, has been fraught with difficulties, because the vast …
Evaluation of lorcaserin as an anticonvulsant in juvenile Fmr1 knockout mice
TS Saraf, DE Felsing, JL Armstrong, RG Booth… - Epilepsy research, 2021 - Elsevier
… K d and K i values report ligand affinities, or how tight a ligand binds to a target, but they are
obtained through different experimental methods; though K d and K i values of a ligand are …
obtained through different experimental methods; though K d and K i values of a ligand are …
Synthesis of novel 5-substituted-2-aminotetralin analogs: 5-HT1A and 5-HT7 G protein-coupled receptor affinity, 3D-QSAR and molecular modeling
… The 5-substituted-2-tetralone analogs 7a-d and 7h-t underwent reductive amination 22 with
dimethylamine to give the racemic 5-SAT analogs 8a-d and 8h-t. Preparative chiral HPLC (…
dimethylamine to give the racemic 5-SAT analogs 8a-d and 8h-t. Preparative chiral HPLC (…