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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References