Soluble in DMSO (~7-10 mg/ml)
A cell-permeable, potent, and selective human A adenosine receptor antagonist (K= 0.66M) and an aurora kinase inhibitor (IC of 30-550 nM for blast colony formation assay). Induces dedifferentiation in murine C2C12 myoblasts. Thye cells were also shown to regain multipluripotency following removal of the compound.
Research or further manufacturing use only, not for food or drug use.