№ files_lp_3_process_9_63219
Supplementary scientific data tables presenting measured solubility values of R406 in multiple buffer systems and its in vitro pharmacological activity profile across diverse non-kinase molecular targets using binding and enzyme assays.
Document type: Supplemental data tables
Subject: R406 solubility and in vitro pharmacological profiling
Compound: R406
Experimental context: Pharmacological profiling experiments
Assay types: Radioligand binding assays; isolated enzyme activity assays
Measured parameters: Solubility (µM); pIC50; pKi
Timepoints: 3 hour; 24 hour
Solvent conditions: 0.1%, 0.3%, and 1% DMSO
Buffer systems: Non-kinase buffers; kinase binding buffer; isolated kinase buffers; phosphate-buffered saline
Target scope: Non-kinase targets across enzyme, receptor, ion channel, and transporter classes
Definitions provided: Inactivity threshold defined as pIC50 of 3.5 (<50% inhibition at 10 µM or non-reproducible activity)
Price: 8 / 10 USD
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