BDBM50450428 CHEMBL4173160

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

InChI Key InChIKey=GOVULXJSIPFVAO-NKNNOBQVSA-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 = 50450428   

TargetHyaluronan mediated motility receptor(Homo sapiens)
Western University

Curated by ChEMBL
LigandPNGBDBM50450428(CHEMBL4173160)
Affinity DataKd:  289nMAssay 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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHyaluronan mediated motility receptor(Homo sapiens)
Western University

Curated by ChEMBL
LigandPNGBDBM50450428(CHEMBL4173160)
Affinity DataKd:  211nMAssay Description:Inhibition of recombinant RHAMM (unknown origin) binding to HA after 240 secs by SPR methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed