[CAS NO. 215543-92-3]  SU5402

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PRODUCTS SPECIFICATIONS [215543-92-3]

Store
Catalog
SLK-S7667
Brand
Selleck
CAS
215543-92-3

DESCRIPTION [215543-92-3]

Overview

MDLMFCD08235144
Molecular Weight296.32
Molecular FormulaC17H16N2O3
SMILESC(=C1C=2C(NC1=O)=CC=CC2)C3=C(CCC(O)=O)C(C)=CN3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM3.3747 mL16.8737 mL33.7473 mL
5 mM0.6749 mL3.3747 mL6.7495 mL
10 mM0.3375 mL1.6874 mL3.3747 mL
50 mM0.0675 mL0.3375 mL0.6749 mL

Description

SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively.

Targets

VEGFR2 [1]
(Cell-free assay)
FGFR1 [1]
(Cell-free assay)
PDGFRβ [1]
(Cell-free assay)
20 nM30 nM510 nM

In vitro

SU5402 inhibits VEGF-, FGF-, PDGF- dependent cell proliferation with IC50 of 0.05 μM, 2.80μM, 28.4 μM, respectively. In HUVECs, SU5416 selectively inhibits VEGF-driven mitogenesis in a dose-dependent manner with IC50 of 0.04 μM. In nasopharyngeal epithelial cells, SU5402 attenuates LMP1-mediated aerobic glycolysis, cellular transformation, cell migration, and invasion. In mouse C3H10T1/2 cells, SU 5402 diminishes the effect of FGF23 on cell differentiation.

In vivo

In mice, SU5416 (25 mg/kg, i.p.) inhibits subcutaneous growth of a panel of tumor cell lines by inhibiting the angiogenic process associated with tumor growth.


Synonyms

1H-Pyrrole-3-propanoic acid, 2-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-4-methyl-
2-[(1,2-Dihydro-2-oxo-3H-indol-3-ylidene)methyl]-4-methyl-1H-pyrrole-3-propanoic acid
SU 5402
3-[3-(2-Carboxyethyl)-4-methylpyrrol-2-methylidenyl]-2-indolinone