BDBM50272613 2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihydro-1,5-benzothiazepine::CHEMBL498539

SMILES Oc1cccc(c1)C1=Nc2ccccc2SC(C1)c1ccc(Cl)cc1

InChI Key InChIKey=GJRNUXBFTTXFHD-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50272613   

TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50272613(2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihy...)
Affinity DataIC50:  1.88E+4nMAssay Description:Inhibition of Electrophorus electricus (electric eel) acetylcholinesterase (AChE) using acetylthiocholine iodide as substrate preincubated for 15 minMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50272613(2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihy...)
Affinity DataIC50:  7.69E+4nMAssay Description:Inhibition of BChE (unknown origin) using butyrylthiocholine chloride as substrate preincubated for 15 minMore data for this Ligand-Target Pair
In DepthDetails Article
TargetAcetylcholinesterase(Homo sapiens (Human))
Quaid-I-Azam University

Curated by ChEMBL
LigandPNGBDBM50272613(2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihy...)
Affinity DataIC50:  1.88E+4nMAssay Description:Inhibition of AchE (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50272613(2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihy...)
Affinity DataIC50:  7.96E+4nMAssay Description:Inhibition of BchE (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50272613(2-(4''-Chlorophenyl)-4-(3'-hydroxyphenyl)-2,3-dihy...)
Affinity DataIC50:  7.66E+4nMAssay Description:Inhibition of BChE (unknown origin) using BCh iodide as substrate preincubated for 15 mins prior to substrate addition measured after 10 mins by Ellm...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed