null

SMILES CCOc1ccc(cc1)S(=O)(=O)N(CC(=O)NN=Cc1ccccc1O)c1ccc(C)cc1

InChI Key InChIKey=BMXMBAWTAZIUJK-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50178213   

TargetOxytocin receptor(Homo sapiens (Human))
Serono Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50178213(4-ethoxy-N-{2-[2-(2-hydroxybenzylidene)hydrazino]-...)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Displacement of [125I]OVTA antagonist from human oxytocin receptor expressed in HEK293-EBNA cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8TN3PubMed
TargetVasopressin V1a receptor(Homo sapiens (Human))
Serono Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50178213(4-ethoxy-N-{2-[2-(2-hydroxybenzylidene)hydrazino]-...)copy SMILEScopy InChI
Affinity DataKi:  3.22E+3nMAssay Description:Displacement of [125I]LVA antagonist from human vasopressin 1a receptor expressed in HEK293-EBNA cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8TN3PubMed