BDBM50603437 CHEMBL5186704

SMILES CC(C)C[C@H](NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)CNC(=O)CCCCNC(=O)CCCCNC(=O)CCCCNC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(N)=O

InChI Key InChIKey=TXBRXRMMIUKLOR-HIXGFQDXSA-N

Data  1 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50603437   

TargetNeuropeptides B/W receptor type 1(Homo sapiens (Human))
Rti International

Curated by ChEMBL
LigandPNGBDBM50603437(CHEMBL5186704)
Affinity DataIC50:  840nMAssay Description:Antagonist activity at human NPBWR1 expressed in CHO-RD-HGA16 cells measured by calcium mobilization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetNeuropeptides B/W receptor type 1(Homo sapiens (Human))
Rti International

Curated by ChEMBL
LigandPNGBDBM50603437(CHEMBL5186704)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human NPBWR1 expressed in CHO-RD-HGA16 cells measured by calcium mobilization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed