null

SMILES CCc1cc(=O)[nH]c(n1)-n1nc(C)cc1NC(=O)c1cccc(C)c1

InChI Key

  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 = 50604204   

Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))TBA
LigandPNGBDBM50604204(CHEMBL5188949)copy SMILES
Affinity DataKi:  900nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RWWPubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))TBA
LigandPNGBDBM50604204(CHEMBL5188949)copy SMILES
Affinity DataIC50: 420nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RWWPubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))TBA
LigandPNGBDBM50604204(CHEMBL5188949)copy SMILES
Affinity DataIC50: 410nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RWWPubMed
TargetAdenylate cyclase type 8(Homo sapiens (Human))TBA
LigandPNGBDBM50604204(CHEMBL5188949)copy SMILES
Affinity DataIC50: 2.70E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RWWPubMed