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. 2015 Nov 30;3(6):e00193. doi: 10.1002/prp2.193

Figure 1.

Figure 1

Chemical structures and cellular activities of compound A. (A) Chemical structure of compound A. (B) Compound concentration‐dependent inhibition of TG synthesis in human intestinal epithelial HT‐29. Cells were preincubated with various concentrations of compound A for 30 min followed by [13C18]‐oleic acid incubation. A representative labeled TG species, TG‐[13C18]18:1‐[13C18]18:1‐[13C18]18:1, was used to represent TG levels in the presence of different concentrations of compound A. Results are expressed as mean ± SEM. IC50: 20 ± 0.3 nmol/L.