BDBM50350753 CHEMBL1818303

SMILES CN(C)CCC1CCN(CC1)c1cc(C(=O)NC[C@H]2CC[C@H](CNC(=O)OCC(C)(C)C)CC2)c2ccccc2n1

InChI Key InChIKey=XLFRUWLYCNSABX-UHFFFAOYSA-N

Data  3 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 = 50350753   

TargetAcetyl-CoA carboxylase 2(Human)
Astrazeneca Research and Development

Curated by ChEMBL
LigandPNGBDBM50350753(CHEMBL1818303)
Affinity DataIC50: 130nMAssay Description:Inhibition of human recombinant his-tagged ACC2 expressed in baculovirus/Sf9 cell assessed as inorganic phosphate formation preincubated for 15 mins ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2012
Entry Details Article
PubMed
TargetAcetyl-CoA carboxylase 1(Human)
Astrazeneca Research and Development

Curated by ChEMBL
LigandPNGBDBM50350753(CHEMBL1818303)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant his-tagged ACC1 expressed in baculovirus/Sf9 cell assessed as inorganic phosphate formation preincubated for 15 mins ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2012
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Astrazeneca Research and Development

Curated by ChEMBL
LigandPNGBDBM50350753(CHEMBL1818303)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2012
Entry Details Article
PubMed