PharmaOnco™ SU5402

CAT#: ITS-0622-YT176
Product Type: Inhibitor
Species: Human, Mouse, Rat, Non-Human Primate, Other
Product Overview
SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively. Additionally, SU5402 has been observed to inhibit IL-1 beta-induced MAPK activity.
Applications
Cell Maintenance
Size
1 mg
Chemical Name
2-[(1,2-Dihydro-2-oxo-3H-indol-3-ylidene)methyl]-4-methyl-1H-pyrrole-3-propanoic acid
Cell Type
Cancer Cells and Cell Lines, Hybridomas, Pluripotent Stem Cells
Species
Human, Mouse, Rat, Non-Human Primate, Other
Subtype
FGFR and VEGFR inhibitor
Limitation
Restrictions for research use only. Intended for use by laboratory professionals.
Shelf Life
Stable as supplied until expiry date on label.
Storage
Store at -20°C
Molecular Weight
296.3 g/mol
Format
Solid
For Research Use Only | Not For Clinical Use
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