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. 2003 Aug;14(8):3254–3265. doi: 10.1091/mbc.E02-12-0809

Table 2.

Inhibition of various chain length BODIPY-LacCer analogs in rat fibroblasts

% Inhibition
BODIPY-SL analogs Nystatin CPZ
C12 So, C5-BODIPY-LacCer 78.7 ± 11.2 9.8 ± 0.9
C16 So, C5-BODIPY-LacCer 80.8 ± 10.2 10.3 ± 1.1
C18 So, C5-BODIPY-LacCer 75.2 ± 8.9 9.3 ± 1.2
C20 So, C5-BODIPY-LacCer 75.9 ± 6.8 8.2 ± 1.2
C18 So, C3-BODIPY-LacCer 84.3 ± 9.4 5.4 ± 0.3

Cells were pretreated with or without the indicated inhibitor (see MATERIALS AND METHODS) and subsequently incubated with the indicated BODIPY-SL (see Figure 1 for structures) as described in Table 1. Values are mean ± SD of at least 10 cells in each of the three independent experiments. so, sphingosine.