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Vatalanib, Free Base

A potent inhibitor of the VEGFR tyrosine kinases
Catalog #: 2026
SKU-Size Size Price Qty
2026-5 5 mg
$70.00
2026-25 25 mg
$235.00
More Sizes Get Quote

Product Details

Alternate Name CGP-79787; PTK 787; ZK222584
Appearance Off-white solid
CAS # 212141-54-3
Molecular Formula C₂₀H₁₅ClN₄
Molecular Weight 346.81
Purity ≥98% by HPLC
Solubility DMSO (25 mg/ml) or EtOH (~ 6 mg/ml)
SMILES C1=CC=C2C(=C1)C(=NN=C2NC3=CC=C(C=C3)Cl)CC4=CC=NC=C4
InChi InChI=1S/C20H15ClN4/c21-15-5-7-16(8-6-15)23-20-18-4-2-1-3-17(18)19(24-25-20)13-14-9-11-22-12-10-14/h1-12H,13H2,(H,23,25)
InChi Key YCOYDOIWSSHVCK-UHFFFAOYSA-N
PubChem CID 151194
MDL Number MFCD08458963
Handling Protect from air and moisture
Storage Conditions -20°C
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.

Details

Cell-permeable. An inhibitor of the VEGFR tyrosine kinases VEGFR-1 (Flt-1, IC₅₀ = 77 nM) and VEGFR-2 (FLK-1/KDR, IC₅₀ = 37 nM), with slightly higher potency against the latter. At higher concentrations, other tyrosine kinases are also inhibited, including PDGFR-β (IC₅₀ = 580 nM), c-KIT (IC₅₀ = 730 nM), FLT-4 (IC₅₀ = 660 nM) and c-FMS (IC₅₀ = 1.4 µM). On the other hand, vatalanib is not active against the EGFR, c-SRC, v-ABL, and protein kinase Cα (IC₅₀ > 10 µM).


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