BDBM50065386 CHEMBL3401327

SMILES Cl.S=C(NCCCNCCCCCNCCCNC(=S)NCCC(c1ccccc1)c1ccccc1)NCCC(c1ccccc1)c1ccccc1

InChI Key InChIKey=BYFZQRFZCVZFHG-UHFFFAOYSA-N

Data  1 KI  3 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 4 hits for monomerid = 50065386   

TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
John Hopkins University

Curated by ChEMBL
LigandPNGBDBM50065386(CHEMBL3401327)
Affinity DataKi:  2.40E+3nMAssay Description:Competitive inhibition of human recombinant LSD1 by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
John Hopkins University

Curated by ChEMBL
LigandPNGBDBM50065386(CHEMBL3401327)
Affinity DataIC50:  1.90E+4nMAssay Description:Inhibition of MAO-B (unknown origin) by MAo-Glo kit analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
John Hopkins University

Curated by ChEMBL
LigandPNGBDBM50065386(CHEMBL3401327)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of MAO-A (unknown origin) by MAo-Glo kit analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysine-specific histone demethylase 1A(Homo sapiens (Human))
John Hopkins University

Curated by ChEMBL
LigandPNGBDBM50065386(CHEMBL3401327)
Affinity DataIC50:  4.80E+3nMAssay Description:Inhibition of human recombinant LSD1 after 30 mins to 4 hrs by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed