BDBM50603467 CHEMBL5197385

SMILES CC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)CNC(=O)CCCCNC(=O)CCCCNC(=O)CCCCNC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(N)=O

InChI Key InChIKey=MHZIAJWURHRTFV-YYQNIRDASA-N

Data  2 EC50

  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 = 50603467   

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

Curated by ChEMBL
LigandPNGBDBM50603467(CHEMBL5197385)
Affinity DataEC50:  5.5nMAssay Description:Agonist activity at human NPBWR1 expressed in CHO cells measured by LANCE Ultra cAMP kit-based TR-FRET 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
LigandPNGBDBM50603467(CHEMBL5197385)
Affinity DataEC50:  25nMAssay 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