SHP244 is a conformational inhibitor targeting the latch allosteric site (site 2) of the SHP2 protein with an IC50 value for SHP2WT of 60 µM. SHP244 has no significant effect on the level of p-ERK alone. SHP244 combined with RMC-4550 (HY-116009) (tunnel site site 1 inhibitor) can reduce p-ERK and inhibit the rebound of p-ERK, thereby reducing drug resistance. SHP244 can be used to study drug resistance in FGFR-driven cancers[1].
Molecular Weight:
432.86
CAS Number:
[902891-37-6]
Formula:
C23H17ClN4O3
Target:
SHP2
Application Notes:
MCE Product type: Reference compound
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