null

SMILES CC(C)(C)C(=O)CN1c2ccccc2N(C2CCCCCC2)C(=O)N(CC(=O)Nc2cccc(c2)-c2nc(=O)o[nH]2)C1=O

InChI Key InChIKey=ZRTOSCLSAJLFLV-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 = 50411975   

TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50411975(CHEMBL5270943)copy SMILEScopy InChI
Affinity DataKd:  2.00E+5nMAssay Description:Displacement of [125I]angiotensin 2 from type-1 angiotensin 2 receptor in Bos taurus (bovine) adrenal cortical membraneMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50411975(CHEMBL5270943)copy SMILEScopy InChI
Affinity DataKd:  7.00E+3nMAssay Description:Inhibition of Manduca sexta V-ATPase V1/Vo holoenzyme activity assessed as inorganic phosphate production pretreated for 5 minsMore data for this Ligand-Target Pair
In DepthDetails