SU5402

CAS No. 215543-92-3

SU5402( SU5402 | SU-5402 | SU 5402 )

Catalog No. M17435 CAS No. 215543-92-3

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.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 62 In Stock
5MG 56 In Stock
10MG 86 In Stock
25MG 161 In Stock
50MG 262 In Stock
100MG 368 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SU5402
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    SU5402 is a potent and selective vascular endothelial growth factor receptor (VEGFR) and fibroblast growth factor receptor (FGFR) inhibitor (IC50 values are 0.02, 0.03, 0.51 and > 100 μ M at VEGFR2, FGFR1, PDGFR β and EGFR respectively).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SU5402 | SU-5402 | SU 5402
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    FGFR1| PDGFRβ| VEGFR2
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    215543-92-3
  • Formula Weight
    296.32
  • Molecular Formula
    C17H16N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 30 mg/mL; 101.24 mM
  • SMILES
    CC1=CNC(=C1CCC(=O)O)/C=C\2/C3=CC=CC=C3NC2=O
  • Chemical Name
    (Z)-3-(4-methyl-2-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoic acid.

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

molnova catalog
related products
  • UNC0631

    UNC0631 is a effectvie histone methyltransferase G9a inhibitor (IC50=4 nM).

  • Dihydroberberine

    Dihydroberberine has anti-atherosclerotic anti-inflammatory hypolipidemic and antitumor activities. It inhibits human ether-a-go-go-related gene (hERG) channels and remarkably reduces Hsp90 expression and its interaction with hERG.

  • Benidipine hydrochlo...

    Benidipine HCl is a hydrochloride salt form of benidipine which is a dihydropyridine calcium channel blocker.