1951466-83-3

YF-452 Chemical Structure
1951466-83-3

Chemical Structure

YF-452

  • CAS No.: 1951466-83-3
  • Formula:C24H26BrN3O
  • Molecular Weight:452.39

IUPAC Name: 1-(9-(4-bromobenzyl)-1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl)-2-(pyrrolidin-1-yl)ethan-1-one

InChIKey: WIRUYQFUVBBWPT-UHFFFAOYSA-N

SMILES: BrC1=CC=C(CN(C2=C3C=CC=C2)C4=C3CCN(C4)C(CN5CCCC5)=O)C=C1

Biological Activity: YF-452 is a potent inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2). YF-452 remarkably inhibits the migration, invasion and tube-like structure formation of human umbilical vein endothelial cells (HUVECs) with little toxicity. YF-452 inhibits VEGF-induced phosphorylation of VEGFR2 kinase and the downstream protein kinases including extracellular signal regulated kinase (ERK), focal adhesion kinase (FAK) and Src. YF-452 is a potential antiangiogenic agent candidate for cancer research[1].

Cat. No. Product Name Purity Description Pricing
HY-120200
YF-452 YF-452 is a potent inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2). YF-452 remarkably inhibits the migration, invasion and tube-like structure formation of human umbilical vein endothelial cells (HUVECs) with little toxicity. YF-452 inhibits VEGF-induced phosphorylation of VEGFR2 kinase and the downstream protein kinases including extracellular signal regulated kinase (ERK), focal adhesion kinase (FAK) and Src. YF-452 is a potential antiangiogenic agent candidate for cancer research.
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