null

SMILES CCOc1ccc(C[C@H]2NC(=O)[C@@H](N)CSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC2=O)[C@@H](C)CC)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CC(C)C)C(=O)NCC(N)=O)cc1

InChI Key InChIKey=DBEFVIUHZSNDLS-QWRNYUHBSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50411358   

TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50411358(CHEMBL5268053)copy SMILEScopy InChI
Affinity DataKd:  3.70E+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
LigandPNGBDBM50411358(CHEMBL5268053)copy SMILEScopy InChI
Affinity DataKd:  3.40E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails