Infigratinib

TargetMol
Product Code: TAR-T1975
Supplier: TargetMol
CodeSizePrice
TAR-T1975-5mg5mg£102.00
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TAR-T1975-1mL1 mL * 10 mM (in DMSO)£105.00
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TAR-T1975-10mg10mg£115.00
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TAR-T1975-25mg25mg£136.00
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TAR-T1975-50mg50mg£148.00
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TAR-T1975-100mg100mg£195.00
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TAR-T1975-200mg200mg£302.00
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TAR-T1975-500mg500mg£460.00
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Infigratinib (BGJ398) is an orally bioavailable pan FGFR inhibitor (IC50: 0.9/1.4/1 nM for FGFR1/2/3), >40-fold selective for FGFR versus FGFR4 and VEGFR2.
CAS:
872511-34-7
Formula:
C26H31Cl2N7O3
Molecular Weight:
560.48
Pathway:
Angiogenesis; Tyrosine Kinase/Adaptors; Apoptosis
Purity:
0.9846
SMILES:
CCN1CCN(CC1)c1ccc(Nc2cc(ncn2)N(C)C(=O)Nc2c(Cl)c(OC)cc(OC)c2Cl)cc1
Target:
Apoptosis; FGFR

References

1. Guagnano V, et al. Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase. J Med Chem. 2011 Oct 27;54(20):7066-83. 2. Guagnano V, et al. FGFR genetic alterations predict for sensitivity to NVP-BGJ398, a selective pan-FGFR inhibitor. Cancer Discov. 2012 Dec;2(12):1118-33. 3. Konecny GE, et al. Activity of the fibroblast growth factor receptor inhibitors dovitinib (TKI258) and NVP-BGJ398 in human endometrial cancer cells. Mol Cancer Ther. 2013 May;12(5):632-42. 4. Lin H, Lu P, Zhou M, et al. Purification of recombinant human fibroblast growth factor 13 in E. coli and its molecular mechanism of mitogenesis[J]. Applied microbiology and biotechnology. 2019: 1-11. 5. Pu X, Ye Q, Cai J, et al. Typing FGFR2 translocation determines the response to targeted therapy of intrahepatic cholangiocarcinomas[J]. Cell death & disease. 2021, 12(3): 1-14.