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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: Bioorg Med Chem. 2013 Mar 7;21(9):2503–2510. doi: 10.1016/j.bmc.2013.02.042

Figure 3.

Figure 3

Concentration response of compound 5 on SK1 activity. Substrates were 3 μM sphingosine and 250 μM ATP (n = 3, results expressed as mean inhibition +/− S.E.). The control is set at 100% and represents the SK1 activity against sphingosine alone.