BDBM50105564 6-(3-Chloro-phenyl)-3H-benzothiazol-2-one::CHEMBL94053

SMILES O=c1[nH]c2ccc(-c3cccc(Cl)c3)cc2s1

InChI Key InChIKey=RFTDPFXJASAPPG-UHFFFAOYSA-N

Data  1 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 3 hits for monomerid = 50105564   

TargetProgesterone receptor(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50105564BDBM50105564(6-(3-Chloro-phenyl)-3H-benzothiazol-2-one | CHEMBL...)
Affinity DataKi:  127nMAssay Description:Binding affinity towards progesterone receptor was measuredMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/4/2012
Entry Details Article
PubMed
TargetProgesterone receptor(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50105564BDBM50105564(6-(3-Chloro-phenyl)-3H-benzothiazol-2-one | CHEMBL...)
Affinity DataIC50: 265nMAssay Description:Inhibitory concentration against progesterone induced PRE-luciferase activity in CV-cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/4/2012
Entry Details Article
PubMed
TargetProgesterone receptor(Human)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50105564BDBM50105564(6-(3-Chloro-phenyl)-3H-benzothiazol-2-one | CHEMBL...)
Affinity DataIC50: 460nMAssay Description:Inhibitory concentration against progesterone stimulated alkaline phosphatase activity in T47D human breast carcinoma cell lineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/4/2012
Entry Details Article
PubMed