null

SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(CC)cc2)NC(=O)CCSSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC1=O)C(=O)NC(C)(C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(N)=O

InChI Key InChIKey=ONPHDFZBCZCBOB-IEFDJERHSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50411355   

TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50411355(CHEMBL5282155)copy SMILEScopy InChI
Affinity DataKd:  6.30E+4nMAssay 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
LigandPNGBDBM50411355(CHEMBL5282155)copy SMILEScopy InChI
Affinity DataKd:  3.80E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails