BDBM50594952 CHEMBL5177724

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)C1(CCCCC1)NC(=O)[C@H](CCCCN(C)[C@@H]1C[C@H]1c1ccccc1)NC(=O)C1(CCCCC1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)N)[C@@H](C)O)C(O)=O

InChI Key InChIKey=VSMBVOXVYRKHBG-UHFFFAOYSA-N

Data  1 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 1 hit for monomerid = 50594952   

TargetLysine-specific histone demethylase 1A(Human)
Hangzhou Normal University

Curated by ChEMBL
LigandPNGBDBM50594952(CHEMBL5177724)
Affinity DataIC50: 58nMAssay Description:Inhibition of recombinant human KMD1A using H3K4Me2 peptide as substrate preincubated for 15 mins followed by substrate addition measured after 30 mi...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/21/2023
Entry Details
PubMed