BDBM50530867 CHEMBL4472654

SMILES [H][C@]12Nc3ccccc3[C@]1([C@H](O)[C@]13SS[C@](C)(N(C)C1=O)C(=O)N23)[C@]12[C@H](O)[C@]34SS[C@](C)(N(C)C3=O)C(=O)N4[C@@]1([H])Nc1ccccc21

InChI Key InChIKey=IMGTYEJTVRXGLW-UHFFFAOYSA-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 = 50530867   

TargetHistone-lysine N-methyltransferase 2A(Human)
University of North Carolina At Greensboro

Curated by ChEMBL
LigandPNGBDBM50530867(CHEMBL4472654)
Affinity DataIC50: 800nMAssay Description:Inhibition of human recombinant MLL1 using [3H]S-adenosyl-methionine as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/26/2021
Entry Details Article
PubMed
TargetHistone-lysine N-methyltransferase 2A(Human)
University of North Carolina At Greensboro

Curated by ChEMBL
LigandPNGBDBM50530867(CHEMBL4472654)
Affinity DataIC50: 800nMAssay Description:Inhibition of human recombinant MLL1 using [3H]S-adenosyl-methionine as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/26/2021
Entry Details Article
PubMed