BDBM50333669 CHEMBL1643384

SMILES C[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2ccc(NN=C(Cc3cnc[nH]3)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc3ccccc3)NC1=O)[C@@H](C)O)cc2)NC(=O)CNC(=O)[C@H](C)N

InChI Key InChIKey=SHIIRGJOLVETGS-UHFFFAOYSA-N

Data  2 IC50

  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 = 50333669   

TargetSomatostatin receptor type 2(Human)
The Weizmann Institute of Science

Curated by ChEMBL
LigandPNGBDBM50333669(CHEMBL1643384)
Affinity DataIC50: 8.10nMAssay Description:Displacement of [125I-Tyr3]octreotide from sst2 receptor expressed in rat AR4-2J cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2011
Entry Details Article
PubMed
TargetSomatostatin receptor type 2(Human)
The Weizmann Institute of Science

Curated by ChEMBL
LigandPNGBDBM50333669(CHEMBL1643384)
Affinity DataIC50: 8.10nMAssay Description:Displacement of [125I-Tyr3]octreotide from sst2 receptor expressed in rat AR4-2J cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2011
Entry Details Article
PubMed