17 articles for JL Kristensen
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Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites.

University of Copenhagen
Synthesis and pharmacological evaluation of N-benzyl substituted 4-bromo-2,5-dimethoxyphenethylamines as 5-HT2A/2C partial agonists.

University of Copenhagen
Tying up Nicotine: New Selective Competitive Antagonist of the Neuronal Nicotinic Acetylcholine Receptors.

University of Copenhagen
Design, synthesis, and biological evaluation of Erythrina alkaloid analogues as neuronal nicotinic acetylcholine receptor antagonists.

University of Copenhagen
Synthesis and SAR study of a novel series of dopamine receptor agonists.

University of Copenhagen
Inhibitor scaffold for the histone lysine demethylase KDM4C (JMJD2C).

University of Copenhagen
Novel 4-(piperidin-4-yl)-1-hydroxypyrazoles as gamma-aminobutyric acid(A) receptor ligands: synthesis, pharmacology, and structure-activity relationships.

University of Copenhagen
N-Hydroxypyrazolyl glycine derivatives as selective N-methyl-D-aspartic acid receptor ligands.

University of Copenhagen
Inhibitors of histone demethylases.

University of Copenhagen
Exploring the neuroleptic substituent in octoclothepin: potential ligands for positron emission tomography with subnanomolar affinity fora(1)-adrenoceptors.

University of Copenhagen
Discovery and Structure-Activity Relationships of 2,5-Dimethoxyphenylpiperidines as Selective Serotonin 5-HT2A Receptor Agonists.

University of Copenhagen
Introducing Conformational Restraints on 25CN-NBOH: A Selective 5-HT

University of Copenhagen
The Alkaloids from

University of Copenhagen
Discovery of β-Arrestin-Biased 25CN-NBOH-Derived 5-HT

University of Copenhagen
Synthesis and Pharmacological Evaluation of DHβE Analogues as Neuronal Nicotinic Acetylcholine Receptor Antagonists.

University of Copenhagen
Dual Nicotinic Acetylcholine Receptor α4β2 Antagonists/α7 Agonists: Synthesis, Docking Studies, and Pharmacological Evaluation of Tetrahydroisoquinolines and Tetrahydroisoquinolinium Salts.

University of Copenhagen
6-aryl-4-morpholin-1-ylpyridone compounds useful for the treatment of cancer and diabetes

Sprint Bioscience