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Linifanib (ABT-869)

Catalog No. S1003 5 5 3 Customer Review(s) Product Citations2 Product Citation(s)
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Linifanib (ABT-869) Chemical Structure

Bio Information

Linifanib (ABT-869) is a structurally novel, potent RTK and VEGF and PDGF receptor families inhibitor with IC50 of 0.2, 2, 4, and 7 nM for human endothelial cells, PDGFR-β, KDR, and CSF-1R, respectively. It has much less activity (IC50s > 1 μM) against unrelated RTKs, soluble tyrosine kinases, or serine/threonine kinases. In vivo ABT-869 is effective orally in the mechanism-based murine models of VEGF-induced uterine edema (ED50 = 0.5 mg/kg) and corneal angiogenesis ( >50%inhibition, 15 mg/kg ). [1][2] 

References:

[1] Mol Cancer Ther 2006;5:995-1006

[2] Mol Cancer Ther 2006;5:1007-1013

Chemical Information

Molecular Weight (WM): 375.41
Formula:

C21H18FN5O

Solubility(R.T.:25°C): DMSO 75mg/mL 
Water <1mg/mL 
Ethanol <1mg/mL 

Quality Control

View current batch:
H-NMR HPLC H-NMR HPLC

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Linifanib (ABT-869) has been referenced in 2 publications.

TSLP signaling network revealed by SILAC-based phosphoproteomics.
Targeting PDGFR-β in Cholangiocarcinoma.

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Average Customer Review

(3 customer reviews)
  • ;J Pharmacol Exp Ther, 2012, 343(3), 617-27
    Linifanib (ABT-869) purchased from Selleck

  • Data from [Liver Int 2011;32(3), 400-409]
    Linifanib (ABT-869) purchased from Selleck

  • ;Dr. Zhang of Tianjin Medical University
    Linifanib (ABT-869) purchased from Selleck

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;J Pharmacol Exp Ther, 2012, 343(3), 617-27


Click to enlarge

Data from [Liver Int 2011;32(3), 400-409]

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