Ki value

The equilibrium dissociation constant for receptor-ligand binding, reflecting affinity.

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Structure-activity relationships of arylbenzofuran H₃ receptor antagonists
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Antagonist Lipophilicity NMR spectroscopy Selectivity Derivatives Molecular docking Apoptosis Synthetic route Mass spectrometry (MS) IC50 Pharmacophore binding affinity Hydrogen bonding HPLC (high-performance liquid chromatography) NMR (nuclear magnetic resonance) Purification Docking Studies Structure-Activity Relationship (SAR) High-Throughput Screening (HTS) Breast Cancer Metabolic Stability π-π Stacking Cell Cycle Arrest Toxicity Profile In vitro assay SAR (Structure-Activity Relationship) H₃ receptor In vivo study Bioisostere Anti-tumor activity Xenograft model Western blot Electron-Donating Group (EDG) Electron-Withdrawing Group (EWG) Benzoxazepine MTT assay IC₅₀ QSAR (Quantitative SAR)

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