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. 2018 Aug 21;9:3165. doi: 10.1038/s41467-018-05613-7

Table 1.

IC50 for inhibition of ceramide synthases by P053

hCerS1 mCerS1 hCerS2 mCerS2 hCerS4 mCerS5 hCerS6
P053 [2] 0.54 ± 0.06 0.46 ± 0.08 28.6 ± 0.15 18.5 ± 0.12 17.2 ± 0.09 7.2 ± 0.10 11.4 ± 0.17
G024 [1] 6.0 ± 0.10 14.5 ± 0.09 18.0 ± 0.12 24.3 ± 0.22 8.5 ± 0.13
FTY720 9.9 ± 0.07 5.6 ± 0.05 19.1 ± 0.10 10.6 ± 0.13 26.0 ± 0.18 15.0 ± 0.07 5.8 ± 0.20
FB1 0.22 ± 0.05 0.15 ± 0.08 0.92 ± 0.06 0.50 ± 0.05 0.29 ± 0.05

Calculated IC50 values (μM) for inhibition of different human (h) or murine (m) CerS isoforms by P053, G024, FTY720, and FB1. IC50 values were calculated using an inhibitor range from 10 nM–100 μM, as shown in Fig. 1b