LC-SF-14 is a selective dual inhibitor of SHP2 and FGFR (IC50 values are 71.6 and 8.9 nM, respectively). LC-SF-14 inhibits FGFR2-FRS2alpha-SHP2-MAPK signaling and ERK phosphorylation. LC-SF-14 inhibits the proliferation of KATOIII cancer cells (IC50: 9.2 nM). LC-SF-14 has antitumor activity in the SNU-16 xenograft mouse model. LC-SF-14 can be used in FGFR2-driven gastric cancer research[1].
Molekulargewicht:
979.38
Formel:
C44H50Cl3N13O5S
Target-Kategorie:
ERK,FGFR,p38 MAPK,SHP2
Anwendungsbeschreibung:
MCE Product type: Reference compound
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