null
SMILES CCCC[C@H](NC(=O)CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(N)=O
InChI Key InChIKey=QUHYACYUHCKMEC-WOUDKVOTSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 50203779
TargetKiSS-1 receptor(Homo sapiens (Human))
University of Minnesota Health Science Center
Curated by ChEMBL
University of Minnesota Health Science Center
Curated by ChEMBL
Affinity DataKi: 15.8nMAssay Description:Displacement of [125]metastin from metastin receptorMore data for this Ligand-Target Pair
TargetKiSS-1 receptor(Homo sapiens (Human))
University of Minnesota Health Science Center
Curated by ChEMBL
University of Minnesota Health Science Center
Curated by ChEMBL
Affinity DataEC50: 25.8nMAssay Description:Activity at metastin receptor expressed in HEK293 cells by measuring calcium releaseMore data for this Ligand-Target Pair