null

SMILES [#6]-[#8]-c1ccc(-[#6]-[#6]\[#6](-[#8])=[#6]-2/[#6](=O)-[#6](-[#6]\[#6]=[#6](\[#6])-[#6])=[#6]3-[#8]C([#6])([#6])[#6]=[#6]C3([#6]\[#6]=[#6](\[#6])-[#6])[#6]-2=O)cc1-[#8]

InChI Key InChIKey=BCOKIBKYEDKYNI-RWEWTDSWSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50136568   

TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Qiqihar University

Curated by ChEMBL
LigandPNGBDBM50136568(CHEMBL3754570)copy SMILEScopy InChI
Affinity DataKi:  1.23E+4nMAssay Description:Competitive inhibition of human recombinant PTP1B using p-nitrophenyl phosphate as substrate by spectrophotometry based Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C82C4WPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Qiqihar University

Curated by ChEMBL
LigandPNGBDBM50136568(CHEMBL3754570)copy SMILEScopy InChI
Affinity DataIC50: 2.02E+4nMAssay Description:Inhibition of human recombinant PTP1B using p-nitrophenyl phosphate as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C82C4WPubMed