BDBM50282115 CHEMBL4165111

SMILES C[C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCC[N+](C)(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=S)Nc1ccc(C2=C3C=CC(O)=CC3Oc3cc(O)ccc23)c(c1)C(O)=O)[C@@H](C)O)[C@@H](C)O)C(=O)NCC(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(O)=O

InChI Key InChIKey=HDUFEAROPVQRMB-WITLFUPKSA-O

Data  2 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50282115   

TargetLysine-specific demethylase 5A(Human)
University of Connecticut

Curated by ChEMBL
LigandPNGBDBM50282115(CHEMBL4165111)
Affinity DataKd:  800nMAssay Description:Inhibition of JARID1A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone-lysine N-methyltransferase 2A(Human)
University of Connecticut

Curated by ChEMBL
LigandPNGBDBM50282115(CHEMBL4165111)
Affinity DataKd:  2.00E+4nMAssay Description:Binding affinity to 15N-labeled GST-tagged MLL1 PHD3 finger domain (1565 to 1627 residues) (unknown origin) expressed in Escherichia coli Rosetta2 BL...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed