29 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Structure-Based Identification of Novel Ligands Targeting Multiple Sites within a Chemokine-G-Protein-Coupled-Receptor Interface.
University of South Florida
Development of novel ACK1/TNK2 inhibitors using a fragment-based approach.
University of South Florida
2-aralkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor.
University of South Florida
Synthesis and structure-activity relationship studies of 1,3-disubstituted 2-propanols as BACE-1 inhibitors.
University of South Florida
Inhibition of the insulin-like growth factor-1 receptor (IGF1R) tyrosine kinase as a novel cancer therapy approach.
University of South Florida
2-(N'-aralkylidenehydrazino)adenosines: potent and selective coronary vasodilators.
University of South Florida
N6,9-disubstituted adenines: potent, selective antagonists at the A1 adenosine receptor.
University of South Florida
2-Alkoxyadenosines: potent and selective agonists at the coronary artery A2 adenosine receptor.
University of South Florida
Activity of N6-substituted 2-chloroadenosines at A1 and A2 adenosine receptors.
University of South Florida
CNS and antimalarial activity of synthetic meridianin and psammopemmin analogs.
University of South Florida
Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).
University of South Florida
Helical sulfonyl-γ-AApeptides for the inhibition of HIV-1 fusion and HIF-1α signaling.
University of South Florida
Rational Design of Sulfonyl-γ-AApeptides as Highly Potent HIV-1 Fusion Inhibitors with Broad-Spectrum Activity.
University of South Florida
The discovery of cyclic γ-AApeptides as the promising ligands targeting EP2.
University of South Florida
Tuaimenal A, a Meroterpene from the Irish Deep-Sea Soft Coral
University of South Florida
α/Sulfono-γ-AApeptide Hybrid Analogues of Glucagon with Enhanced Stability and Prolonged In Vivo Activity.
University of South Florida
Discovery of Cyclic Peptidomimetic Ligands Targeting the Extracellular Domain of EGFR.
University of South Florida
Rational Design of Right-Handed Heterogeneous Peptidomimetics as Inhibitors of Protein-Protein Interactions.
University of South Florida
α-Helix-Mimicking Sulfono-γ-AApeptide Inhibitors for p53-MDM2/MDMX Protein-Protein Interactions.
University of South Florida
Substituted 1,3-dipropylxanthines as irreversible antagonists of A1 adenosine receptors.
University of South Florida
Linear and proximal benzo-separated alkylated xanthines as adenosine-receptor antagonists.
University of South Florida
2-(N'-alkylidenehydrazino)adenosines: potent and selective coronary vasodilators.
University of South Florida
One-Bead-Two-Compound Thioether Bridged Macrocyclicγ-AApeptide Screening Library against EphA2.
University of South Florida
Flavanone derivatives, and preparation method and use thereof
Xuanwu Hospital of Capital Medical University
Ligand-directed functional heterogeneity of histamine H1 receptors: novel dual-function ligands selectively activate and block H1-mediated phospholipase C and adenylyl cyclase signaling.
University of North Carolina at Chapel Hill