ABT-702 0.1μM R06 exp260

Inhibits adenosine kinase (ADK)

  • Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Compound References

  • PubChem Name: Adenosine Kinase Inhibitor
  • Synonyms: N/A
  • CAS #: 1188890-28-9
  • PubChem CID: 16760265
  • IUPAC: 5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-amine;dihydrochloride
  • INCHI Name: InChI=1S/C22H19BrN6O.2ClH/c23-16-3-1-2-14(10-16)17-11-18(28-22-20(17)21(24)26-13-27-22)15-4-5-19(25-12-15)29-6-8-30-9-7-29;;/h1-5,10-13H,6-9H2,(H2,24,26,27,28);2*1H
  • INCHI Key: OOXNYFKPOPJIOT-UHFFFAOYSA-N
  • Molecular Weight: 536.2
  • Canonical SMILES: C1COCCN1C2=NC=C(C=C2)C3=NC4=NC=NC(=C4C(=C3)C5=CC(=CC=C5)Br)N.Cl.Cl
  • Isomeric SMILES: N/A
  • Molecular Formula: C22H21BrCl2N6O

Compound Supplier

  • Supplier Name: Tocris Bioscience
  • Catalog #: 2372
  • Lot #: 1B/195137

Compound Characterization

  • HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C22H19BrN6O 463.08765; found 463.08744

Dose Response Curve

  • Platform ID: ABT-702
  • Min: -17.1478; Max: 50.6783





IC Concentration (µM)
IC10 N/A
IC20 27.2987
IC30 35.4200
IC40 43.8496
IC50 N/A
IC60 N/A
IC70 N/A
IC80 N/A
IC90 N/A


  • Round: 06
  • Dose: 100nM
  • Days of incubation: 8
  • Doublings: 7.2
  • Numbers of reads: 7476948
Sensitive/Resistant hits (FDR<0.05)CRANKSScore PlotTop 30 GenesScreen SimilarityTop 30 Sensitive GO termsTop 30 Resistant GO terms
0/0ScoresViewViewViewViewView

  • Last modified: 2026/01/15 21:36
  • by 127.0.0.1