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A cell-permeable adenosine analog that acts a potent non-selective agonist of adenosine receptors (Ki = 14 nM, 20 nM
The Adenosine Deaminase Inhibitor, DCF, also referenced under CAS 53910-25-1, controls the biological activity of Adenosine Deaminase.
A key regulator of many cellular reactions.
A blood-brain barrier permeable xanthine derivative that acts as a highly selective antagonist of Adenosine A1 receptor (A1R; Ki
An adenosine analog that acts as a selective, high affinity agonist for Adenosine A1 receptor (A1R) (Ki = 800 pM
A potent and selective agonist of adenosine A1 receptor (A1R) (Ki
A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).
A highly potent and selective antagonist of adenosine A2A receptor (Ki = 6
A xanthin derivative that acts as a potent agonist of adenosine A2A receptors (Ki =
A cell-permeable and reversible inhibitor of protein kinase A (Ki = 11 μM).
Cell-permeable cAMP analog that has greater resistance to phosphodiesterases than cAMP.
This Dibutyryl-cAMP, CAS 16980-89-5, is a cell-permeable cAMP analog that preferentially activates PKA.
A highly selective agonist of adenosine A3 receptor (Ki = 330 pM).
Cell-permeable cAMP analog that activates both protein kinase A and protein kinase G.
A potent, cell-permeable, and reversible metabolically-stable cAMP antagonist that inhibits cAMP-dependent protein kinase and shows preference for PKA type I.