BDBM50222716 CHEMBL2371535

SMILES [H][C@]1(NC(=O)[C@H](CCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H]([C@@H](C)O)C(N)=O)NC(=O)[C@@H](CO)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCC)NC(=O)[C@@H](CO)NC(=O)CN(CCN)C(=O)Oc1cc(\C=C/c2cc(OC)c(OC)c(OC)c2)ccc1OC)[C@@H](C)O

InChI Key InChIKey=KFGZMVCLOTYVJM-RKUUOQTOSA-N

Data  1 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 1 hit for monomerid = 50222716   

TargetSomatostatin receptor type 1/2/3/4/5(Homo sapiens (Human))
Tulane University Health Sciences Center

Curated by ChEMBL
LigandPNGBDBM50222716(CHEMBL2371535)
Affinity DataIC50:  2.80nMAssay Description:Cytotoxic activity against human neuroblastoma IMR32 cells which over-express somatostatin receptorsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed