BDBM50370581 CHEMBL1791310

SMILES CC(O)[C@H]1NC(=O)[C@@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](C)NC(=O)[C@@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](NC(=O)[C@H](Cc2ccccc2)NC1=O)[C@H](C)O)C(N)=O)NC(=O)CNC(=O)[C@H](C)N

InChI Key InChIKey=XOOYWFHODVEJSJ-GXCJHMFDSA-N

Data  2 KI

  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 = 50370581   

TargetSomatostatin receptor type 2(Homo sapiens (Human))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50370581(CHEMBL1791310)
Affinity DataKi:  20nMAssay Description:Inhibition of human somatostatin receptor type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSomatostatin receptor type 4(Homo sapiens (Human))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50370581(CHEMBL1791310)
Affinity DataKi:  80nMAssay Description:Inhibition of human somatostatin receptor type 4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed