null

SMILES CC(NC(=O)\N=C(/N)NCCCc1sc(N)nc1C)c1ccc(C)cc1

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 2 hits for monomerid = 50568752   

TargetHistamine H2 receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50568752(CHEMBL4869194)copy SMILES
Affinity DataKi:  31nMAssay Description:Displacement of [3H]UR-DE257 from human histamine H2 receptor expressed in sf9 insect cell membranes co-expressing GSalphaS incubated for 60 mins by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TF0245PubMed
TargetHistamine H2 receptor(Cavia porcellus (domestic guinea pig))TBA
LigandPNGBDBM50568752(CHEMBL4869194)copy SMILES
Affinity DataEC50:  22nMAssay Description:Agonist activity at guinea pig right atrium histamine H2 receptor assessed as increase in heart rate incubated for 30 mins in presence of cimetidineMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TF0245PubMed