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  • UniPR500: A Comprehensive Technical Guide to its Chemical Structure . . .
    UniPR500 was developed to improve upon the pharmacokinetic profile of its parent compound, exhibiting enhanced metabolic stability and oral bioavailability This technical guide provides a detailed overview of the chemical structure, physicochemical properties, and biological activity of UniPR500 , along with the experimental protocols for its
  • Eph antagonist UniPR500 | C36H51N3O4 | CID 172031705 - PubChem
    Eph antagonist UniPR500 | C36H51N3O4 | CID 172031705 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
  • UniPR500 | EphA2 Receptor Antagonist | MedChemExpress
    UniPR500, a UniPR129 derivative, is a competitive EphA2 receptor antagonist with a K of 0 78 μM UniPR500 dose-dependently reduces binding of biotinylated ephrin-A1 to EphA2 with an IC50 value of 1 1 μM
  • Unipr500|CAS |DC Chemicals
    NCGC00685960 is a Nicotinamide N-methyltransferase (NNMT) inhibitor with an IC50 < 10 nM NCGC00685960 has potent antitumor activity NCGC00685960 increases H3K27 trimethylation levels in ovarian cancer cells and inhibits α-SMA expression in NNMT-expressing ovarian fibroblasts
  • UniPR500_TargetMol
    UniPR500, a derivative of UniPR129, is a competitive antagonist for the EphA2 receptor, with a Ki of 0 78 μM It reduces the binding of biotinylated Ephrin-A1 to EphA2 in a dose-dependent manner, exhibiting an IC50 value of 1 1 μM
  • UniPR500 - prefix CAS No. 2085767-98-0 | Aladdin Scientific
    Home Small Molecules Compound Libraries Signaling Pathways Protein Tyrosine Kinase RTK Ephrin Receptor UniPR500 , CAS No 2085767-98-0 Skip to the end of the images gallery Skip to the beginning of the images gallery
  • Welcome to Hodoodo Chemicals
    Description: UniPR500 is a novel eph antagonist, inhibiting eph ephrin interactions, enhancing glucose-stimulated insulin secretion (gsis), and acting as a hypoglycemic agent
  • UniPR500: A Technical Guide to a Novel EphA5 Receptor Antagonist
    This document details the mechanism of action, binding affinity, and in vitro and in vivo effects of UniPR500, supported by quantitative data, detailed experimental protocols, and visual representations of key biological pathways and experimental workflows
  • UniPR500, AMS. T204989-50-MG | Amsbio
    UniPR500, a derivative of UniPR129, is a competitive antagonist for the EphA2 receptor, with a Ki of 0 78 μM It reduces the binding of biotinylated Ephrin-A1 to EphA2 in a dose-dependent manner, exhibiting an IC50 value of 1 1 μM





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