User profiles for D. Felsing

Dennis Felsing

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Verified email at felsing.org
Cited by 161

Automating regression verification

D Felsing, S Grebing, V Klebanov, P Rümmer… - Proceedings of the 29th …, 2014 - dl.acm.org
… 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. …

Advances in dopamine D1 receptor ligands for neurotherapeutics

DE Felsing, MK Jain, JA Allen - Current topics in medicinal …, 2019 - ingentaconnect.com
The dopamine D1 receptor (D1R) is essential for neurotransmission in various brain pathways
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

CE Canal, DE Felsing, Y Liu, W Zhu… - ACS chemical …, 2015 - ACS Publications
… 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 …

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 …

[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 …

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 …

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-…

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 …

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 …

Synthesis of novel 5-substituted-2-aminotetralin analogs: 5-HT1A and 5-HT7 G protein-coupled receptor affinity, 3D-QSAR and molecular modeling

CK Perry, AB Casey, DE Felsing, R Vemula… - Bioorganic & Medicinal …, 2020 - Elsevier
… 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 (…