BDBM50568529 CHEMBL4851339

SMILES COc1ccc(CNC2CC22CCc3ccccc23)cc1OC

InChI Key InChIKey=QLRUDMCNKCTIBP-UHFFFAOYSA-N

Data  3 IC50

  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 3 hits for monomerid = 50568529   

TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
Key Laboratory Of Henan Provinc

Curated by ChEMBL
LigandPNGBDBM50568529(CHEMBL4851339)
Affinity DataIC50:  3nMAssay Description:Inhibition of human LSD1 (172 to 852 residues) using Bio-H3K4me2 (1 to 24 residues) as substrate incubated for 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Key Laboratory Of Henan Provinc

Curated by ChEMBL
LigandPNGBDBM50568529(CHEMBL4851339)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of human MAO-B expressed in baculovirus infected BTI insect cells by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Key Laboratory Of Henan Provinc

Curated by ChEMBL
LigandPNGBDBM50568529(CHEMBL4851339)
Affinity DataIC50:  1.17E+4nMAssay Description:Inhibition of human MAO-A expressed in baculovirus infected BTI insect cells by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed