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A2AAR antagonist 5

A2AAR antagonist 5

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SKU:QM-0013472

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  • Description

    A2AAR antagonist 5 is a selective A2AAR antagonist. A2AAR antagonist 5 inhibits NECA-stimulated adenylyl cyclase activity in hA2AAR-expressing CHO cells with an IC50 value of 1863 nM. A2AAR antagonist 5 possesses strong free radical scavenging activity, with an EC50 value of 22.21 μM in the DPPH assay. A2AAR antagonist 5 exerts notable neuroprotective effects in in vitro cerebral ischemia models. A2AAR antagonist 5 can be used for the study of cerebral ischemia[1].

  • Molecular Formula

    C23H20N8O3

  • Molecular Weight

    456.46

  • Smiles

    O=C(NC1=CC=C(C2=CN3C(C(N)=N2)=NN(C4=CC=CC=C4)C3=O)C=C1)CN5N=C(C)CC5=O

  • Target

    Adenosine Receptor

  • Isoform

    Adenosine A1 receptor (A1R) ; Adenosine A2A receptor (A2AR) ; Adenosine A2B receptor (A2BR) ; Adenosine A3 receptor (A3R)

  • Shipping Conditions

    Room temperature

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A2AAR antagonist 5

A2AAR antagonist 5 is a premium-grade research compound supplied by Quantimol for laboratory and scientific applications.