null

SMILES C[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](Cc2ccccc2)NC1=O)C(O)=O)N(C)C(=O)c1ccc2ccccc2c1

InChI Key InChIKey=DVUCJCYCSZBIEC-ZYLACCOCSA-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 5 hits for monomerid = 85724   

TargetSomatostatin receptor type 3(Homo sapiens (Human))
University of Berne

Curated by PDSP Ki Database
LigandPNGBDBM85724(des-AA 1,2,4,5,12,13[DAgl8(Me,2-naphthoyl)]-SS)copy SMILEScopy InChI
Affinity DataKi:  70nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N01539PubMed
TargetSomatostatin receptor type 2(Homo sapiens (Human))
University of Berne

Curated by PDSP Ki Database
LigandPNGBDBM85724(des-AA 1,2,4,5,12,13[DAgl8(Me,2-naphthoyl)]-SS)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N01539PubMed
TargetSomatostatin receptor type 5(Homo sapiens (Human))
University of Berne

Curated by PDSP Ki Database
LigandPNGBDBM85724(des-AA 1,2,4,5,12,13[DAgl8(Me,2-naphthoyl)]-SS)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N01539PubMed
TargetSomatostatin receptor type 4(Homo sapiens (Human))
University of Berne

Curated by PDSP Ki Database
LigandPNGBDBM85724(des-AA 1,2,4,5,12,13[DAgl8(Me,2-naphthoyl)]-SS)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N01539PubMed
TargetSomatostatin receptor type 1(Homo sapiens (Human))
University of Berne

Curated by PDSP Ki Database
LigandPNGBDBM85724(des-AA 1,2,4,5,12,13[DAgl8(Me,2-naphthoyl)]-SS)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N01539PubMed