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ABT 702

Axon 2289
Based on 54 publications in PubMed
CAS:  214697-26-4
Purity:  99%
  • Soluble in 0.1N HCl(aq) and DMSO
  • MF:  C22H19BrN6O
  • MW:  463.33

Description

ABT 702 is a potent, non-nucleoside adenosine kinase (ADK) inhibitor with IC50 values of 2 nM in cytosolic assays and 50 nM in intact-cell assays. It is orally active in animal models of pain and inflammation and is used to study pharmacological elevation of endogenous adenosine tone.

Adenosine kinase regulates intracellular and extracellular adenosine availability, influencing purinergic signaling, inflammation and nociception. ABT 702 is useful for exploring ADK-dependent analgesic and anti-inflammatory mechanisms.

Key Features

  • Potent non-nucleoside ADK inhibitor
  • IC50: 2 nM in cytosolic assays
  • Orally active in pain and inflammation models
  • Increases adenosine pathway signaling by ADK inhibition

Applications

  • Adenosine metabolism research
  • Pain and inflammation model studies
  • Purinergic signaling assays
  • ADK inhibitor pharmacology

More Information

Certificate of Analysis

Material Safety Data Sheet

Parent CAS No. 214697-26-4
Chemical Name 5-(3-bromophenyl)-7-(6-morpholinopyridin-3-yl)pyrido[2,3-d]pyrimidin-4-amine
SMILES C1=NC(N)=C2C(C3=CC=CC(Br)=C3)=CC(C3=CC=C(N4CCOCC4)N=C3)=NC2=N1
MFCD MFCD05861333
InChi InChI=1S/C22H19BrN6O/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)
InChiKey RQCXKDWOCUJWQZ-UHFFFAOYSA-N
CID 1973
Short Description ADK inhibitor

References

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