PMID

Data

Article Title

Organization

Cupriphilic compounds to aid in proteasome inhibition.

University of South Florida

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

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

Antiviral enantiomeric preference for 5'-noraristeromycin.

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

Inhibitors of cysteine proteases and methods of use thereof

Pardes Biosciences

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

Ligand specificity of nicotinic acetylcholine receptors in rat spinal cord: studies with nicotine and cytisine.

University of California