An inhibitor of VEGFR2
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VEGFR2 Kinase Inhibitor IV

Item No. 45474

Technical Information
Formal Name
6-(4-methoxyphenyl)-3-(3-thienyl)-pyrazolo[1,5-a]pyrimidine
CAS Number
216661-57-3
Synonyms
  • Vascular Endothelial Growth Factor Receptor 2 Kinase Inhibitor IV
Molecular Formula
C17H13N3OS
Formula Weight
Purity
≥98%
A solid
DMSO: Slightly soluble: 0.1-1 mg/mlMethanol:Chloroform (1:1): Sparingly soluble: 1-10 mg/ml
SMILES
COC1=CC=C(C=C1)C2=CN3N=CC(C4=CSC=C4)=C3N=C2
InChi Code
InChI=1S/C17H13N3OS/c1-21-15-4-2-12(3-5-15)14-8-18-17-16(9-19-20(17)10-14)13-6-7-22-11-13/h2-11H,1H3
InChi Key
HBWLNACPIFKNIP-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    VEGFR2 kinase inhibitor IV is an inhibitor of VEGFR2 (IC50 = 19 nM).1 It is greater than 100-fold selective for VEGFR2 over FGFR1 and Src but only 1.8-, 10-, and 10-fold selective over PDGFRβ, FLT1, and FLT2, respectively. VEGFR2 kinase inhibitor IV inhibits mitogenesis in human umbilical vein endothelial cells (HUVECs; IC50 = 387 nM). It also reduces VEGF-induced increases in neuroglobin levels in primary mouse cerebrocortical neurons when used at a concentration of 20 nM.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Fraley, M.E., Hoffman, W.F., Rubino, R.S., et alSynthesis and initial SAR studies of 3,6-disubstituted pyrazolo[1,5-a]pyrimidines: A new class of KDR kinase inhibitors. Bioorg. Med. Chem. Lett. 12(19), 2767-2770 (2002).

    2. Jin, K., Mao, X., Xie, L., et alInteractions between vascular endothelial growth factor and neuroglobin. Neurosci. Lett. 519(1), 47-50 (2012).