Peder Svensson
Goeteborg, O 41346, Sweden
Last Updated: 09/26/2026
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Found 17 publications
Estimation of Dopamine D1 Receptor Agonist Binding Kinetics Using Time-Resolved Functional Assays: Relation to Agonist-Induced Receptor Internalization by Investigational Antiparkinsonian Therapeutics.
Journal: ACS chemical neuroscience
Published: June 19, 2025
Neurophysiological treatment effects of mesdopetam, pimavanserin and clozapine in a rodent model of Parkinson's disease psychosis.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: December 08, 2023
Rational antibody design for undruggable targets using kinetically controlled biomolecular probes.
Journal: Science advances
Published: September 03, 2020
Preclinical Pharmacology of [2-(3-Fluoro-5-Methanesulfonyl-phenoxy)Ethyl](Propyl)amine (IRL790), a Novel Dopamine Transmission Modulator for the Treatment of Motor and Psychiatric Complications in Parkinson Disease.
Journal: The Journal of pharmacology and experimental therapeutics
Published: December 18, 2019
Hip To Be Square: Oxetanes as Design Elements To Alter Metabolic Pathways.
Journal: Journal of medicinal chemistry
Published: July 17, 2019
Oxetane Substrates of Human Microsomal Epoxide Hydrolase.
Journal: Drug metabolism and disposition: the biological fate of chemicals
Published: April 24, 2017
In Vivo Systems Response Profiling and Multivariate Classification of CNS Active Compounds: A Structured Tool for CNS Drug Discovery.
Journal: ACS chemical neuroscience
Published: December 21, 2016
Behavioral Analysis of Dopaminergic Activation in Zebrafish and Rats Reveals Similar Phenotypes.
Journal: ACS chemical neuroscience
Published: March 08, 2016
State of affairs: Design and structure-activity relationships of reversible P2Y12 receptor antagonists.
Journal: Bioorganic & medicinal chemistry letters
Published: February 03, 2016
Structural and functional characterization of a specific antidote for ticagrelor.
Journal: Blood
Published: January 16, 2015
A novel series of 6-substituted 3-(pyrrolidin-1-ylmethyl)chromen-2-ones as selective monoamine oxidase (MAO) A inhibitors.
Journal: European journal of medicinal chemistry
Published: June 23, 2013
Structure-activity relationship of 5-chloro-2-methyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole analogues as 5-HT(6) receptor agonists.
Journal: European journal of medicinal chemistry
Published: December 12, 2012
Last Updated: 09/26/2026