28 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Synthesis and binding profile of haloperidol-based bivalent ligands targeting dopamine D(2)-like receptors.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Click chemistry based synthesis of dopamine D4 selective receptor ligands for the selection of potential PET tracers.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Functionally selective dopamine D2/D3 receptor agonists comprising an enyne moiety.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Novel azulene derivatives for the treatment of erectile dysfunction.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Discovery of a dopamine D4 selective PET ligand candidate taking advantage of a click chemistry based REM linker.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Clinic of Nuclear Medicine
Synthesis, radiofluorination, and in vitro evaluation of pyrazolo[1,5-a]pyridine-based dopamine D4 receptor ligands: discovery of an inverse agonist radioligand for PET.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
trans-2,3-dihydroxy-6a,7,8,12b-tetrahydro-6H-chromeno[3,4-c]isoquinoline: synthesis, resolution, and preliminary pharmacological characterization of a new dopamine D1 receptor full agonist.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Purdue University
2-[(4-phenylpiperazin-1-yl)methyl]imidazo(di)azines as selective D4-ligands. Induction of penile erection by 2-[4-(2-methoxyphenyl)piperazin-1-ylmethyl]imidazo[1,2-a]pyridine (PIP3EA), a potent and selective D4 partial agonist.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Laboratoire De Chimie Th�Rapeutique
Pharmacophore-guided drug discovery investigations leading to bioactive 5-aminotetrahydropyrazolopyridines. Implications for the binding mode of heterocyclic dopamine D3 receptor agonists.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Fancy bioisosteres: metallocene-derived G-protein-coupled receptor ligands with subnanomolar binding affinity and novel selectivity profiles.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Bivalent molecular probes for dopamine D2-like receptors.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Evaluation of 18F-labeled benzodioxine piperazine-based dopamine D4 receptor ligands: lipophilicity as a determinate of nonspecific binding.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Forschungszentrum J£Lich
Bivalent dopamine D2 receptor ligands: synthesis and binding properties.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Aromatic ring functionalization of benzolactam derivatives: new potent dopamine D3 receptor ligands.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of Santiago De Compostela
Highly potent 5-aminotetrahydropyrazolopyridines: enantioselective dopamine D3 receptor binding, functional selectivity, and analysis of receptor-ligand interactions.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Synthesis, biological evaluation and radiolabelling by 18F-fluoroarylation of a dopamine D3-selective ligand as prospective imaging probe for PET.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander-UniversitäT Erlangen-NüRnberg
Novel pyridylmethylamines as highly selective 5-HT(1A) superagonists.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Bioisosteric replacement leading to biologically active [2.2]paracyclophanes with altered binding profiles for aminergic G-protein-coupled receptors.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
1,1'-Disubstituted ferrocenes as molecular hinges in mono- and bivalent dopamine receptor ligands.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Parallel synthesis of potent dopaminergic N-phenyltriazole carboxamides applying a novel click chemistry based phenol linker.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Novel D3 selective dopaminergics incorporating enyne units as nonaromatic catechol bioisosteres: synthesis, bioactivity, and mutagenesis studies.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Click chemistry based solid phase supported synthesis of dopaminergic phenylacetylenes.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
In vitro affinities of various halogenated benzamide derivatives as potential radioligands for non-invasive quantification of D(2)-like dopamine receptors.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Johannes Gutenberg University
Structure-selectivity investigations of D2-like receptor ligands by CoMFA and CoMSIA guiding the discovery of D3 selective PET radioligands.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Synthesis and biological investigations of dopaminergic partial agonists preferentially recognizing the D4 receptor subtype.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
Friedrich-Alexander University
Synthesis and evaluation of 18F-labeled dopamine D3 receptor ligands as potential PET imaging agents.![EBI](/images/logo_chembl.png)
![EBI](/images/logo_chembl.png)
University of Erlangen-Nuremberg