Product Variations
Product # | Price | Quantity | |
---|---|---|---|
VD-AM-0056-0010-10mg | $140 | ||
VD-AM-0056-0050-50mg | $500 |
$140.00 – $500.00
Orange-red solid
5812-07-7
VD-AM-0056
C17H16N2O
264.32
≥98% (HPLC)
Soluble to 30 mg/mL in DMSO
-20°C. Air and light sensitive.
DMBI; 3-[[4-(dimethylamino)phenyl] methylene]-1,3-dihydro-2H-indol-2-one
10mg, 50mg
Product # | Price | Quantity | |
---|---|---|---|
VD-AM-0056-0010-10mg | $140 | ||
VD-AM-0056-0050-50mg | $500 |
SU 4312 (CAS 5812-07-7) is a cell-permeable, reversible, ATP-competitive, and potent inhibitor of the tyrosine kinase activities of the PDGF β-receptor (β-PDGFR; IC50 = 4 µM in PAC-1 cells) and FGFR1 (IC50 = 5 µM for inhibition of tyrosine phosphorylation of p90). Does not inhibit EGFR or c-Src tyrosine kinases, even at concentrations greater than 100 µM.
1. Zaman et al (1998) Biochem.Pharmacol. 57 57.
2. Sun et al (1998) J.Med.Chem. 41 2588.
3. Kendall et al (1999) J.Biol.Chem. 274 6453.
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