BDBM50313483 CHEMBL1091089::H-KPPR-OH

SMILES [#7]-[#6]-[#6]-[#6]-[#6]-[#6@H](-[#7])-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](-[#8])=O

InChI Key InChIKey=CKFCCXJQYNXYHI-QAETUUGQSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50313483   

TargetNeuropilin-1(Human)
University of Warsaw

Curated by ChEMBL
LigandPNGBDBM50313483(CHEMBL1091089 | H-KPPR-OH)
Affinity DataIC50:  4.60E+3nMAssay Description:Inhibition of biotinylated VEGF165 binding to NRP1 (unknown origin) by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeuropilin-1(Human)
University of Warsaw

Curated by ChEMBL
LigandPNGBDBM50313483(CHEMBL1091089 | H-KPPR-OH)
Affinity DataIC50:  1.40E+4nMAssay Description:Displacement of [125I]VEGF-A from human NRP1 expressed in pig aortic endothelial cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed