null

SMILES CSCC[C@H](NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CO)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=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)NC1=O)[C@@H](C)O)[C@@H](C)O)C(O)=O

InChI Key InChIKey=GGYTXJNZMFRSLX-DFTNLTQTSA-N

  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 3 hits for monomerid = 50254239   

TargetSomatostatin receptor type 5(Homo sapiens (Human))
McGill University

Curated by PDSP Ki Database
LigandPNGBDBM50254239(somatostatin-28)copy SMILEScopy InChI
Affinity DataKi:  0.0700nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959G27PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
McGill University

Curated by PDSP Ki Database
LigandPNGBDBM50254239(somatostatin-28)copy SMILEScopy InChI
Affinity DataKi:  0.290nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X065KZPubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
McGill University

Curated by PDSP Ki Database
LigandPNGBDBM50254239(somatostatin-28)copy SMILEScopy InChI
Affinity DataKi:  0.390nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ02B7PubMed