BDBM50210050 CHEMBL3884529

SMILES CC(C)C[C@@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CO)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CCCN2C(=O)OCCCCCCOC(=O)NCCCC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](NC1=O)C(C)C)C(=O)N1CCC[C@H]1C(N)=O

InChI Key InChIKey=JNENCPWHZPHTBT-UHFFFAOYSA-N

Data  2 KI

  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 = 50210050   

TargetLysine-specific histone demethylase 1A(Human)
Nagoya City University

Curated by ChEMBL
LigandPNGBDBM50210050(CHEMBL3884529)
Affinity DataKi: >3.00E+5nMAssay Description:Inhibition of human LSD1 assessed as reduction in H2O2 production using H3K4me2 (1 to 20 residues) peptide as substrate preincubated for 10 mins foll...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/6/2018
Entry Details Article
PubMed
TargetLysine-specific histone demethylase 1A(Human)
Nagoya City University

Curated by ChEMBL
LigandPNGBDBM50210050(CHEMBL3884529)
Affinity DataKi: >3.00E+5nMAssay Description:Inhibition of human LSD1 assessed as reduction in H2O2 production using H3K4me2 (1 to 20 residues) peptide as substrate preincubated for 10 mins foll...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/6/2018
Entry Details Article
PubMed