BDBM50251697 CHEMBL4093222

SMILES O=C1C=CC(=O)c2c1ccc1c3ccc4ccccc4c3oc(=O)c21

InChI Key InChIKey=BAKYVKJVQXJPSV-UHFFFAOYSA-N

Data  3 IC50  1 Kd

  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 4 hits for monomerid = 50251697   

TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM50251697(CHEMBL4093222)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of recombinant human full length GST-tagged CDC25A expressed in Escherichia coli BL21-DE3 pLysS using 3-O-methylfluorescein phosphate as s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetArylsulfatase A(Homo sapiens)
Jinan Second People'S Hospital

Curated by ChEMBL
LigandPNGBDBM50251697(CHEMBL4093222)
Affinity DataKd:  2.10E+4nMAssay Description:Binding affinity to ARSA (unknown origin) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetArylsulfatase A(Homo sapiens)
Jinan Second People'S Hospital

Curated by ChEMBL
LigandPNGBDBM50251697(CHEMBL4093222)
Affinity DataIC50:  1.32E+4nMAssay Description:Inhibition of ARSA (unknown origin) using 4-methylumbelliferyl sulfate (4-MUS) as a substrate by fluorescent assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Sapienza University of Rome

Curated by ChEMBL
LigandPNGBDBM50251697(CHEMBL4093222)
Affinity DataIC50:  100nMAssay Description:Compound was evaluated for its ability to displace [3H]-cytisine binding from high-affinity Nicotinic acetylcholine receptor in rat brain (principall...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed