BDBM50450431 CHEMBL4170615

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

InChI Key InChIKey=NWLMJPMZRXEOBB-DNMUGYPRSA-N

Data  2 Kd

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50450431   

TargetHyaluronan mediated motility receptor(Homo sapiens)
Western University

Curated by ChEMBL
LigandPNGBDBM50450431(CHEMBL4170615)
Affinity DataKd:  33nMAssay 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
TargetHyaluronan mediated motility receptor(Homo sapiens)
Western University

Curated by ChEMBL
LigandPNGBDBM50450431(CHEMBL4170615)
Affinity DataKd:  202nMAssay 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