18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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A potent and selective inhibitor for the UBLCP1 proteasome phosphatase.

Indiana University
Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors.

Indiana University
Design, synthesis, biochemical studies, cellular characterization, and structure-based computational studies of small molecules targeting the urokinase receptor.

Indiana University
Bicyclic benzofuran and indole-based salicylic acids as protein tyrosine phosphatase inhibitors.

Indiana University
A new glucagon and GLP-1 co-agonist eliminates obesity in rodents.

Indiana University
Amino- and guanidinoacylryanodines: basic ryanodine esters with enhanced affinity for the sarcoplasmic reticulum Ca(2+)-release channel.

Indiana University
Small molecule inhibitors of SHP2 tyrosine phosphatase discovered by virtual screening.

Indiana University
Comprehensive in vitro analysis of voriconazole inhibition of eight cytochrome P450 (CYP) enzymes: major effect on CYPs 2B6, 2C9, 2C19, and 3A.

Indiana University
Structure-Activity Relationship Study of Cannabidiol-Based Analogs as Negative Allosteric Modulators of the μ-Opioid Receptor.

Indiana University
Small-Molecule Cyanamide Pan-TEAD·YAP1 Covalent Antagonists.

Indiana University
Optimization of Truncated Glucagon Peptides to Achieve Selective, High Potency, Full Antagonists.

Indiana University
Pyridyl-alanine as a Hydrophilic, Aromatic Element in Peptide Structural Optimization.

Indiana University
Targeting the HSP60/10 chaperonin systems of Trypanosoma brucei as a strategy for treating African sleeping sickness.

Indiana University
GroEL/ES inhibitors as potential antibiotics.

Indiana University
A biochemical screen for GroEL/GroES inhibitors.

Indiana University
Screening serine/threonine and tyrosine kinase inhibitors for histidine kinase inhibition.

Indiana University
Hydroxamic Acid Compound Having ENPP1 Inhibitory Activity and Use Thereof

Haihe Biopharma
Systems-based design of bi-ligand inhibitors of oxidoreductases: filling the chemical proteomic toolbox.

Triad Therapeutics