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Cat. No. Product Name Information
PC-45537

Erdafitinib

FGFR inhibitor

Erdafitinib (JNJ-42756493) is a highly potent and selective, small-molecule inhibitor of FGFR family with IC50s of 1.2/2.5/3/5.7 nM for FGFR1/2/3/4.
PC-42406

FGF-401

FGFR4 inhibitor

FGF-401 (NVP-FGF401, Roblitinib, FGF401) is a first-in-class, potent, highly selective FGFR4 inhibitor with IC50 of 1.1 nM.
PC-28678

CYY292

FGFR1 inhibitor

CYY292 is a potent and selective FGFR1 inhibitor with IC50 of 28, 28, and 78 nM for FGFR1, FGFR2, and FGFR3, does not inhibit FGFR4, alters FGFR1 phosphorylation both exogenously and endogenously through the negative feedback effect of Ser777.
PC-26972

KNT-0919

FGFR2/3 inhibitor

KNT-0919 is a potent, selective and covalent FGFR2/3 inhibitor, potently suppresses FGFR2- and FGFR3-driven Ba/F3 cells with IC50 of 1.1 nM and 0.20 nM respectively.
PC-26356

SOMCL-286

FGFR/VEGFR inhibitor

SOMCL-286 (Compound 25a) is a highly potent dual FGFR/VEGFR inhibitor with IC50 of 1.0 nM against FGFR1, shows nearly equally high potency against FGFR1, FGFR2 and VEGFR-2 with IC50 values of 1.0, 4.5 and 2.9 nM, respectively.
PC-26355

SOMCL-085

FGFR inhibitor

SOMCL-085 is a potent multi-targeted FGFR inhibitor with IC50 of 1.8, 1.9 and 6.9 nM for FGFR1-3, simultaneously inhibits VEGFR and PDGFR.
PC-26084

FGFR3 covalent inhibitor 10s

FGFR3 inhibitor

FGFR3 covalent inhibitor 10s is a selective, covalent FGFR3 inhibitor with IC50 of 6.8 nM, has 5-60-fold selectivity over FGFR1/2/4.
PC-25243

TCB-32

bFGF mimic, FGFR1 activator

TCB-32 is an agonistic small molecules that mimic binding of basic fibroblast growth factor (bFGF), shows a strong proliferative effect in NIH 3T3 cells, activates the same FGFR1-signaling pathway as bFGF.
PC-22625

FGF trap compound 57

FGF trap inhibitor

FGF trap compound 57 is a non-steroidal NSC12 derivative as FGF trap small molecule, shows anti-myeloma activity.

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