BDBM50087141 (E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-yl)-octahydroinden-4-ylidene)acetic acid::CHEMBL332036::[(1R,7aR)-1-((R)-1,5-Dimethyl-hexyl)-7a-methyl-octahydro-inden-(4E)-ylidene]-acetic acid

SMILES CC(C)CCC[C@@H](C)[C@H]1CCC2\C(CCC[C@]12C)=C\C(O)=O

InChI Key InChIKey=FVZJAPUDDDBSCR-MYLZYLCNSA-N

Data  6 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50087141   

TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  7.70E+3nMAssay Description:Concentration required for the inhibitory activity against human Cell division cycle 25AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  8.00E+3nMAssay Description:Concentration required to inhibit human Cell division cycle 25B activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of human Cdc25A phosphatase activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  5.90E+3nMAssay Description:Inhibitory concentration agaunst dual-specificity phosphatase Cell division cycle (Cdc) 25BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  1.72E+4nMAssay Description:Inhibitory concentration againsts dual-specificity phosphatase Cell division cycle (Cdc) 25AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50087141((E)-2-((1R,7aR)-7a-methyl-1-((R)-6-methylheptan-2-...)
Affinity DataIC50:  5.50E+3nMAssay Description:Concentration required to inhibit human Cell division cycle 25A activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed