BDBM50450433 CHEMBL4162476

SMILES CSCC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(N)=O

InChI Key InChIKey=NPSYXADPVZABAH-UHFFFAOYSA-N

Data  2 Kd

  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 = 50450433   

TargetHyaluronan mediated motility receptor(Human)
Western University

Curated by ChEMBL
LigandPNGBDBM50450433(CHEMBL4162476)
Affinity DataKd:  21nMAssay Description:Inhibition of C-terminal His-tagged 7 kDa RHAMM (unknown origin) binding to HA after 240 secs by SPR methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed
TargetHyaluronan mediated motility receptor(Human)
Western University

Curated by ChEMBL
LigandPNGBDBM50450433(CHEMBL4162476)
Affinity DataKd:  30nMAssay Description:Inhibition of recombinant RHAMM (unknown origin) binding to HA after 240 secs by SPR methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/15/2020
Entry Details Article
PubMed