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Merck
CN

572631

SU5402

InSolution, ≥95%, Inhibits the tyrosine kinase activity of FGFR1

别名:

InSolution SU5402, SU5402

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关于此项目

线性分子式:
C17H16N2O3
NACRES:
NA.77
UNSPSC Code:
12352200
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产品名称

SU5402, InSolution, ≥95%, Inhibits the tyrosine kinase activity of FGFR1

assay

≥95% (HPLC)

form

liquid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)
protect from light

storage temp.

−70°C

Quality Level

Disclaimer

Toxicity: Irritant (B)

General description

Inhibits the tyrosine kinase activity of FGFR1 (IC50 = 10-20 µM in the presence of 1 mM ATP) by interacting with the catalytic domain of FGFR1. Also inhibits aFGF-induced phosphorylation of ERK1 and ERK2 (IC50 = 10-20 µM). In contrast to SU4984, it acts only as a weak inhibitor of tyrosine phosphorylation of the PDGF receptor. Does not inhibit the phosphorylation of insulin receptor and exhibits no inhibitory effect on EGF receptor kinase.

Legal Information

Not available for sale in the United States.
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Other Notes

Mohammadi, M., et al. 1997. Science 276, 955.

Packaging

Packaged under inert gas

Physical form

A 10 mM (500 µg/169 µl) solution of SU5402 (Cat. No. 572630) in DMSO.

Preparation Note

Following initial thaw, aliquot and freeze (-70°C).

存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

188.6 °F - (refers to pure substance)

flash_point_c

87 °C - (refers to pure substance)


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Lydvina Meister et al.
Development (Cambridge, England), 149(10) (2022-05-17)
The fibroblast growth factor (FGF) signalling pathway plays various roles during vertebrate embryogenesis, from mesoderm formation to brain patterning. This diversity of functions relies on the fact that vertebrates possess the largest FGF gene complement among metazoans. In the cephalochordate

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