P2L-003 is a selective PAR2 antagonist with an IC 50 of 0.62 μM in HT-29 cells. P2L-003 blocks PAR2 -mediated Ca 2+ mobilization without affecting PAR1 , PAR4 , or ATP -mediated signaling and dose-dependently suppresses the downstream MAPK signaling cascades, including ERK1/2 and p38 phosphorylation. P2L-003 can be used for colon cancer research.
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