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

  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 = 50203779   

TargetKiSS-1 receptor(Homo sapiens (Human))
University of Minnesota Health Science Center

Curated by ChEMBL
LigandPNGBDBM50203779((2S)-2-{[(2S)-1-[(2S)-2-amino-4-methylpentanoyl]py...)copy SMILEScopy InChI
Affinity DataKi:  15.8nMAssay Description:Displacement of [125]metastin from metastin receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2P0KPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
University of Minnesota Health Science Center

Curated by ChEMBL
LigandPNGBDBM50203779((2S)-2-{[(2S)-1-[(2S)-2-amino-4-methylpentanoyl]py...)copy SMILEScopy InChI
Affinity DataEC50:  25.8nMAssay Description:Activity at metastin receptor expressed in HEK293 cells by measuring calcium releaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HT2P0KPubMed