BDBM50205688 CHEMBL3975325

SMILES c1ccc(cc1)-c1nccc2c3ccccc3[nH]c12

InChI Key InChIKey=WOHXZRIXRLZSBI-UHFFFAOYSA-N

Data  2 KI  2 IC50

  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 = 50205688   

Target5-hydroxytryptamine receptor 5A(Homo sapiens (Human))TBA
LigandPNGBDBM50205688(CHEMBL3975325)
Affinity DataKi:  1.40E+3nMAssay Description:Binding affinity to 5-HT5AR (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In DepthDetails PubMed
Target5-hydroxytryptamine receptor 2B(Homo sapiens (Human))TBA
LigandPNGBDBM50205688(CHEMBL3975325)
Affinity DataKi:  1.40E+3nMAssay Description:Binding affinity to 5-HT2BR (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCholinesterase(Homo sapiens (Human))
University Of Massachusetts Boston

Curated by ChEMBL
LigandPNGBDBM50205688(CHEMBL3975325)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of BuChE (unknown origin) by spectrophotometric analysis based Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Nanjing Medical University

Curated by ChEMBL
LigandPNGBDBM50205688(CHEMBL3975325)
Affinity DataIC50:  7.24E+3nMAssay Description:Inhibition of TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-tryptophan as substrate incubated for 75 mins by UV ...More data for this Ligand-Target Pair
In DepthDetails PubMed