DCP Logo
  • Home
  • About
    • DCP program
    • DCP program history
    • Structural Genomic Consortium
    • Probe contributions
  • Show Probes
    • All
    • Kinase
    • GPCR
    • Ion channel
    • Epigenetics
    • Other enzymes
    • Other targets
  • Order set
  • Download
  • Information
    • FAQ
    • Probe resources
    • Donate probes
    • Contact
    • Funding
    • Update history
All probes Probe criteria Further information Usage Order Properties Structure Compound analysis Potency Selectivity Data download
  • Probe criteria
  • Further information
  • Usage
  • Order
  • Properties
  • Structure
  • Compound analysis
  • Potency
  • Selectivity
  • Data download

Potency data for probe (R)-9s and control (S)-9s


In vitro potency


Target name Target information Species Assay description (R)-9s (S)-9s Publication of assay conditions
ADRA1D Homo sapiens Binding assay (ADRA1D) Ki = 1.6 nM (n=3) Ki = 130 nM (n=3) PMID: 26954848
ADRA1A Homo sapiens Binding assay (ADRA1A) Ki > 2700 nM (n=3) PMID: 26954848
ADRA1B Homo sapiens Binding assay (ADRA1B) Ki > 1200 nM (n=3) PMID: 26954848


In cell potency


Target name Target information Species Assay description (R)-9s (S)-9s Publication of assay conditions
rat bladder strips Rattus sp. Inhibition of phenylephrine-induced contractions in bladder strips from rats with bladder outlet obstruction IC30 = 15 nM PMID: 26954848