null

SMILES CCCCc1ncc(\C=C(/Cc2cccs2)C(O)=O)n1Cc1ccccc1[N+]([O-])=O

InChI Key InChIKey=ZQIOEYNQFIXWJE-SFQUDFHCSA-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 = 50011974   

LigandPNGBDBM50011974(3-[2-Butyl-3-(2-nitro-benzyl)-3H-imidazol-4-yl]-2-...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Inhibition of [125I]AII binding to Angiotensin II receptor, type 1 of rat mesenteric arteriesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PK0JC7PubMed
TargetType-2 angiotensin II receptor(RAT)
SmithKline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50011974(3-[2-Butyl-3-(2-nitro-benzyl)-3H-imidazol-4-yl]-2-...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:In vitro inhibition of [125I]-AII specific binding towards Angiotensin II receptor in rat mesenteric membranes.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TD9WBVPubMed