null

SMILES CC(C)CN(NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCCN)C(N)=O

InChI Key InChIKey=UFRTUGJWFAJUSD-WCTYMAGYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50394984   

TargetPlatelet glycoprotein 4(Rattus norvegicus)
Universit£ de Montr£al

Curated by ChEMBL
LigandPNGBDBM50394984(CHEMBL2163465)copy SMILEScopy InChI
Affinity DataIC50: 1.05E+4nMAssay Description:Displacement of photoactivatable [125I]-Tyr-Bpa-Ala-Hexarelin from CD36 in Sprague-Dawley rat cardiac membranes incubated for 60 mins by densitometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6D00PubMed
TargetGrowth hormone secretagogue receptor type 1(Homo sapiens (Human))
Universit£ de Montr£al

Curated by ChEMBL
LigandPNGBDBM50394984(CHEMBL2163465)copy SMILEScopy InChI
Affinity DataIC50: 5.41E+3nMAssay Description:Displacement of [125I]ghrelin expressed in in LLC-PK1 cells incubated for 1 hr by gamma counting methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22J6D00PubMed