null

SMILES Cc1cccc2[nH]c(cc12)C(=O)c1cc2cc(OCCN3CCCCC3)ccc2[nH]1

InChI Key InChIKey=QAKBRLMMNDWGCC-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50187357   

TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
University of Regensburg

Curated by ChEMBL
LigandPNGBDBM50187357((4-Methyl-1H-indol-2-yl)-[5-(2-piperidin-1-yl-etho...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of endogenous FLT3 in EOL1 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0M7BPubMed
TargetPlatelet-derived growth factor receptor alpha/beta(Mus musculus (mouse))
University of Regensburg

Curated by ChEMBL
LigandPNGBDBM50187357((4-Methyl-1H-indol-2-yl)-[5-(2-piperidin-1-yl-etho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of endogenous PDGFR in Swiss3T3 fibroblastsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0M7BPubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
University of Regensburg

Curated by ChEMBL
LigandPNGBDBM50187357((4-Methyl-1H-indol-2-yl)-[5-(2-piperidin-1-yl-etho...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human FLT3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0M7BPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
University of Regensburg

Curated by ChEMBL
LigandPNGBDBM50187357((4-Methyl-1H-indol-2-yl)-[5-(2-piperidin-1-yl-etho...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of human PDGFR betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0M7BPubMed