null

SMILES [#6]\[#6](-[#6])=[#6]\[#6]-c1c(oc2c3-[#6]=[#6]C([#6])([#6])[#8]-c3cc(-[#8])c2c1=O)-c1ccc(-[#8])cc1-[#8]

InChI Key InChIKey=XFFOMNJIDRDDLQ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50242014   

TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Universidade Federal de Santa Catarina

Curated by ChEMBL
LigandPNGBDBM50242014(CHEMBL464006 | Morusin | Morusin, 3 | TCMDC-124149...)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+4nMAssay Description:Inhibition of human PTP1B using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured every minute fo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4F79PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Universidade Federal de Santa Catarina

Curated by ChEMBL
LigandPNGBDBM50242014(CHEMBL464006 | Morusin | Morusin, 3 | TCMDC-124149...)copy SMILEScopy InChI
Affinity DataIC50: 2.21E+4nMAssay Description:Inhibition of recombinant PTP1B catalytic domain (unknown origin) assessed as reduction in pNP formation using pNPP as substrate by absorbance based ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2125XGZPubMed