A3AR antagonist 4
A3AR antagonist 4 (Compd 1) is an A3AR antagonist, with Ki values of 30.8 nM (hA3) and 203 nM (hA1), repectively. A3AR antagonist 4 (Compd 1) can be used for the study of cerebral ischemia[1].
Product Specifications
CAS Number
[109740-09-2]
UNSPSC
12352005
Hazard Statement
H302, H315, H320, H335
Target
Adenosine Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/a3ar-antagonist-4.html
Purity
99.98
Solubility
10 mM in DMSO
Smiles
O=C1NC2=C(C=CC=C2)C3=CN(C4=CC=CC=C4)N=C13
Molecular Formula
C16H11N3O
Molecular Weight
261.28
Precautions
H302, H315, H320, H335
References & Citations
[1]Vittoria Colotta, et al. New 2-arylpyrazolo[3,4-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonists. Synthesis, pharmacological evaluation, and ligand-receptor modeling studies. J Med Chem. 2007 Aug 23;50 (17) :4061-74.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Available Sizes
Curated Selection
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