A pan-FGFR inhibitor
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LY2874455

Item No. 20843

Technical Information
Formal Name
4-[(1E)-2-[5-[(1R)-1-(3,5-dichloro-4-pyridinyl)ethoxy]-1H-indazol-3-yl]ethenyl]-1H-pyrazole-1-ethanol
CAS Number
1254473-64-7
Molecular Formula
C21H19Cl2N5O2
Formula Weight
Purity
≥98%
A crystalline solid
λmax
222, 279, 333 nm
SMILES
ClC1=C([C@@H](C)OC2=CC(C(/C=C/C3=CN(CCO)N=C3)=NN4)=C4C=C2)C(Cl)=CN=C1
InChi Code
InChI=1S/C21H19Cl2N5O2/c1-13(21-17(22)10-24-11-18(21)23)30-15-3-5-20-16(8-15)19(26-27-20)4-2-14-9-25-28(12-14)6-7-29/h2-5,8-13,29H,6-7H2,1H3,(H,26,27)/b4-2+/t13-/m1/s1
InChi Key
GKJCVYLDJWTWQU-CXLRFSCWSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    LY2874455 is a pan-inhibitor of fibroblast growth factor receptor (FGFR) tyrosine kinases with IC50 values of 2.8, 2.6, 6.4, 6, and 7 nM for FGFR1, FGFR2, FGFR3, FGFR4, and VEGFR2, respectively.1 It has been shown to inhibit proliferation of KMS-11, OPM-2, SNU-16, and KATO-III cancer cells in vitro and in tumor xenografts in mice.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Zhao, G., Li, W.-y., Chen, D., et alA novel, selective inhibitor of fibroblast growth factor receptors that shows a potent broad spectrum of antitumor activity in several tumor xenograft models. Mol. Cancer Ther. 10(11), 2200-2210 (2011).