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Characteristics
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A cell-permeable, potent, and selective human A3 adenosine receptor antagonist (Ki = 0.66 µM) and an aurora kinase inhibitor (IC50's of 30-550 nM for blast colony formation assay). Induces dedifferentiation in murine C2C12 myoblasts. The cells were also shown to regain multipluripotency following removal of the compound.
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