16 articles for B Capuano
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Proof of concept study for designed multiple ligands targeting the dopamine D2, serotonin 5-HT2A, and muscarinic M1 acetylcholine receptors.
Monash University (Parkville Campus)
Synthesis and pharmacological evaluation of dual acting ligands targeting the adenosine A2A and dopamine D2 receptors for the potential treatment of Parkinson's disease.
Monash University (Parkville Campus)
Structure-activity relationships of privileged structures lead to the discovery of novel biased ligands at the dopamine D2 receptor.
Monash University
Synthesis and pharmacological evaluation of analogues of benzyl quinolone carboxylic acid (BQCA) designed to bind irreversibly to an allosteric site of the M1 muscarinic acetylcholine receptor.
Monash University (Parkville Campus)
A structure-activity analysis of biased agonism at the dopamine D2 receptor.
Monash University (Parkville Campus)
Homobivalent ligands of the atypical antipsychotic clozapine: design, synthesis, and pharmacological evaluation.
Monash University (Parkville Campus)
Synthesis and SAR study of 4-arylpiperidines and 4-aryl-1,2,3,6-tetrahydropyridines as 5-HT2C agonists.
Monash University (Parkville Campus)
The design, synthesis and biological evaluation of novel URB602 analogues as potential monoacylglycerol lipase inhibitors.
Monash University (Parkville Campus)
Rapid Elaboration of Fragments into Leads Applied to Bromodomain-3 Extra-Terminal Domain.
Monash University (Parkville Campus)
The Design, Synthesis, and Evaluation of Novel 9-Arylxanthenedione-Based Allosteric Modulators for the δ
Monash University (Parkville Campus)
Rapid Elaboration of Fragments into Leads by X-ray Crystallographic Screening of Parallel Chemical Libraries (REFiL
Monash University (Parkville Campus)
Structure-Kinetic Profiling of Haloperidol Analogues at the Human Dopamine D
University of Nottingham
Probing structural requirements of positive allosteric modulators of the M4 muscarinic receptor.
Monash University
Synthesis and pharmacological profiling of analogues of benzyl quinolone carboxylic acid (BQCA) as allosteric modulators of the M1 muscarinic receptor.
Monash University
Novel adenosine A(2A) receptor ligands: a synthetic, functional and computational investigation of selected literature adenosine A(2A) receptor antagonists for extending into extracellular space.
Monash University (Parkville Campus)