BDBM50455453 CHEMBL2079558

SMILES CC(C)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](Cc1ccc2ccccc2c1)C(N)=O)NC(=O)[C@H](N)Cc1ccc2ccccc2c1

InChI Key InChIKey=WASLGBPOQJKRMS-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50455453   

TargetSomatostatin receptor type 2(Human)
Tulane University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50455453(CHEMBL2079558)
Affinity DataIC50: 139nMAssay Description:Binding affinity towards cloned human somatostatin 2 (hsst) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2012
Entry Details Article
PubMed
TargetSomatostatin receptor type 4(Human)
Tulane University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50455453(CHEMBL2079558)
Affinity DataIC50: 1.00E+3nMAssay Description:Binding affinity towards cloned human somatostatin 4 (hsst) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2012
Entry Details Article
PubMed
TargetSomatostatin receptor type 3(Human)
Tulane University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50455453(CHEMBL2079558)
Affinity DataIC50: 1.00E+3nMAssay Description:Binding affinity towards cloned human somatostatin 3 (hsst) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2012
Entry Details Article
PubMed
TargetSomatostatin receptor type 1(Human)
Tulane University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50455453(CHEMBL2079558)
Affinity DataIC50: 1.00E+3nMAssay Description:Binding affinity towards cloned human somatostatin 1 (hsst) receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2012
Entry Details Article
PubMed