14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and evaluation of novel tropane derivatives as potential PET imaging agents for the dopamine transporter.

Beijing Normal University
Structure-Activity Relationships of Cyano-substituted Indole Derivatives as Ligands for α-Synuclein Aggregates.

Beijing Normal University
Design and Characterization of Squaramic Acid-Based Prostate-Specific Membrane Antigen Inhibitors for Prostate Cancer.

Beijing Normal University
Positron Emission Tomography (PET) Imaging Tracers for Serotonin Receptors.

Beijing Normal University
Novel quinazoline derivatives bearing various 6-benzamide moieties as highly selective and potent EGFR inhibitors.

Beijing Normal University
Synthesis and evaluation of novel radioiodinated PSMA targeting ligands for potential radiotherapy of prostate cancer.

Beijing Normal University
Novel natural compounds from endophytic fungi with anticancer activity.

Beijing Normal University
Novel promising 4-anilinoquinazoline-based derivatives as multi-target RTKs inhibitors: Design, molecular docking, synthesis, and antitumor activities in vitro and vivo.

Beijing Normal University
Preliminary evaluation of fluoro-pegylated benzyloxybenzenes for quantification of β-amyloid plaques by positron emission tomography.

Beijing Normal University
Radioiodinated benzyloxybenzene derivatives: a class of flexible ligands target to β-amyloid plaques in Alzheimer's brains.

Beijing Normal University
Synthesis and biological evaluation of 18F-labled 2-phenylindole derivatives as PET imaging probes for β-amyloid plaques.

Beijing Normal University
Novel anilinophthalimide derivatives as potential probes for beta-amyloid plaque in the brain.

Beijing Normal University
A highly potent CDK4/6 inhibitor was rationally designed to overcome blood brain barrier in gliobastoma therapy.

Beijing Normal University
Development of a series of novel 4-anlinoquinazoline derivatives possessing quinazoline skeleton: Design, synthesis, EGFR kinase inhibitory efficacy, and evaluation of anticancer activities in vitro.

Beijing Normal University