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BW710

BW710 is a potent and selective oral inhibitor of FGFR2, with an IC50 of 2.8 nM in cellular assays. It demonstrates promising oral bioavailability (29% in mice) and is a valuable tool for investigating FGFR2-driven oncogenesis in both in vitro and in vivo cancer research models.

Product Specifications

Field of Research

Cardiovascular Research, Signal Transduction

Molecular Formula

C28H29FN6O2S

Molecular Weight

532.63

Storage Conditions

-20°C

Notes

For research use only.

Available Sizes

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