null

SMILES OC(=O)c1cccc(c1)-c1ccc(\C=C2/SC(=S)NC2=O)o1

InChI Key InChIKey=BHFPIPOWNHCUDR-GHXNOFRVSA-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 3 hits for monomerid = 50189763   

TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The University of Jordan

Curated by ChEMBL
LigandPNGBDBM50189763(3-(5-((4-oxo-2-thioxothiazolidin-5-ylidene)methyl)...)copy SMILEScopy InChI
Affinity DataIC50: 920nMAssay Description:Inhibition of PI3Kgamma (unknown origin) assessed as decrease in fluorescence intensity using phosphorylated substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057HM8PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The University of Jordan

Curated by ChEMBL
LigandPNGBDBM50189763(3-(5-((4-oxo-2-thioxothiazolidin-5-ylidene)methyl)...)copy SMILEScopy InChI
Affinity DataIC50: 920nMAssay Description:Inhibition of human PI3KgammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ07X0PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
Serono Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50189763(3-(5-((4-oxo-2-thioxothiazolidin-5-ylidene)methyl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of human PI3KalphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ07X0PubMed