BDBM50300030 6,7-Dimaethoxy-2-(4-methylpiperazin-1-yl)-N-(1-methylpiperidin-4-yl)quinazolin-4-amine::6,7-dimethoxy-2-(4-methylpiperazin-1-yl)-N-(1-methylpiperidin-4-yl)quinazolin-4-amine::CHEMBL572373

SMILES COc1cc2nc(nc(NC3CCN(C)CC3)c2cc1OC)N1CCN(C)CC1

InChI Key InChIKey=IZHGEBMDDQJOEW-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50300030   

TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
University Of North Carolina

Curated by ChEMBL
LigandPNGBDBM50300030(6,7-Dimaethoxy-2-(4-methylpiperazin-1-yl)-N-(1-met...)
Affinity DataIC50:  200nMAssay Description:Inhibition of G9a by Alpha screen assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
University Of North Carolina

Curated by ChEMBL
LigandPNGBDBM50300030(6,7-Dimaethoxy-2-(4-methylpiperazin-1-yl)-N-(1-met...)
Affinity DataIC50:  1.50E+5nMAssay Description:Activity at methyl transferase activity G9a by enzyme coupled S-adenocylehomocystein detection assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
University Of North Carolina

Curated by ChEMBL
LigandPNGBDBM50300030(6,7-Dimaethoxy-2-(4-methylpiperazin-1-yl)-N-(1-met...)
Affinity DataIC50:  680nMAssay Description:Inhibition of G9a by Alpha screen assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
University Of North Carolina

Curated by ChEMBL
LigandPNGBDBM50300030(6,7-Dimaethoxy-2-(4-methylpiperazin-1-yl)-N-(1-met...)
Affinity DataIC50:  2.00E+5nMAssay Description:Inhibition of methyl transferase activity of G9a assessed as inhibition of H3K9 methylation by chemiluminescence based oxygen tunneling assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed