null

SMILES CCC1(OCC(=O)Nc2ccc(cc12)-c1ccc(C#N)n1C)c1cccs1

InChI Key InChIKey=DOUYVHLXGYRPAP-UHFFFAOYSA-N

  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 2 hits for monomerid = 50264312   

TargetProgesterone receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50264312(5-(5-ethyl-2-oxo-5-(thiophen-2-yl)-1,2,3,5-tetrahy...)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:Displacement of [3H]progesterone from progesterone receptor in human T47D cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B03D7PubMed
TargetProgesterone receptor(Homo sapiens (Human))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50264312(5-(5-ethyl-2-oxo-5-(thiophen-2-yl)-1,2,3,5-tetrahy...)copy SMILEScopy InChI
Affinity DataIC50: 14.6nMAssay Description:Antagonist activity at progesterone receptor assessed as progesterone-induced alkaline phosphatase activity in human T47D cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B03D7PubMed