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FGFR-IN-11

FGFR-IN-11
FGFR-IN-11 (compound I-5) is an orally active, covalent inhibitor of FGFR, with IC50 values of 9.9 nM (FGFR1), 3.1 nM (FGFR2), 16 nM (FGFR3), and 1.8 nM (FGFR4). This compound demonstrates nanomolar potency in inhibiting the proliferation of various cancer cells and significantly hinders tumor growth in xenograft mouse models [1].
Catalog No. T79257Cas No. 2658488-68-5

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FGFR-IN-11

Catalog No. T79257Cas No. 2658488-68-5

FGFR-IN-11 (compound I-5) is an orally active, covalent inhibitor of FGFR, with IC50 values of 9.9 nM (FGFR1), 3.1 nM (FGFR2), 16 nM (FGFR3), and 1.8 nM (FGFR4). This compound demonstrates nanomolar potency in inhibiting the proliferation of various cancer cells and significantly hinders tumor growth in xenograft mouse models [1].
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Pack SizePriceAvailabilityQuantity
25 mg$1,8208-10 weeks
50 mg$2,3808-10 weeks
100 mg$3,1008-10 weeks
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Product Introduction

Bioactivity
Description
FGFR-IN-11 (compound I-5) is an orally active, covalent inhibitor of FGFR, with IC50 values of 9.9 nM (FGFR1), 3.1 nM (FGFR2), 16 nM (FGFR3), and 1.8 nM (FGFR4). This compound demonstrates nanomolar potency in inhibiting the proliferation of various cancer cells and significantly hinders tumor growth in xenograft mouse models [1].
Targets&IC50
FGFR4:1.8 nM, FGFR3:16 nM, FGFR2:3.1 nM, FGFR1:9.9 nM
In vitro
FGFR-IN-11, at concentrations ranging from 0.3 nM to 20 μM over a 72-hour period, effectively inhibits the growth of various cancer cell lines [1].
In vivo
FGFR-IN-11, administered orally at a dose of 60 mg/kg daily for 21 days, significantly inhibited tumor growth in female nude mouse xenograft models of Huh-7 or NCI-H1581 without affecting the mouse body weight. [1]
Chemical Properties
Molecular Weight521.01
FormulaC28H29ClN4O4
Cas No.2658488-68-5
Storage & Solubility Information
StorageShipping with blue ice.

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