null

SMILES CC(C(=O)NC1CC1C)c1ccc(O[C@@H]2CCN(C2)c2ncnc(OCC(C)(F)F)c2F)cc1

InChI Key InChIKey=BKLDPPGZLFZGFY-LZUQWOSISA-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 = 212623   

TargetAcetyl-CoA carboxylase 2 [129-967](Homo sapiens (Human))
Boehringer Ingelheim International GmbH

US Patent
LigandPNGBDBM212623(US9278954, 1.14 | US9278954, 1.22)copy SMILEScopy InChI
Affinity DataIC50: 311nMpH: 7.5Assay Description:Malonyl CoA formation by acetyl CoA carboxylases is stoichometrically linked to the consumption of ATP. ACC2 activity is measured in a NADH-linked ki...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RB73FMUS Patent
TargetAcetyl-CoA carboxylase 2 [129-967](Homo sapiens (Human))
Boehringer Ingelheim International GmbH

US Patent
LigandPNGBDBM212623(US9278954, 1.14 | US9278954, 1.22)copy SMILEScopy InChI
Affinity DataIC50: 244nMpH: 7.5Assay Description:Malonyl CoA formation by acetyl CoA carboxylases is stoichometrically linked to the consumption of ATP. ACC2 activity is measured in a NADH-linked ki...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RB73FMUS Patent