Compile Data Set for Download or QSAR
Report error Found 172 Enz. Inhib. hit(s) with all data for entry = 7719
TargetAcetyl-CoA carboxylase 2 [129-967](Human)
Boehringer Ingelheim International

US Patent
LigandChemical structure of BindingDB Monomer ID 212757BDBM212757(US9278954, 7.1)
Affinity DataIC50: 41nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212754BDBM212754(US9278954, 6.8 isomer 2 | US9278954, 7.34 | US9278...)
Affinity DataIC50: 43nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212610BDBM212610(US9278954, 6.1 isomer 2 | US9278954, 6.1 isomer 1 ...)
Affinity DataIC50: 57nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212611BDBM212611(US9278954, 1.2)
Affinity DataIC50: 61nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212759BDBM212759(US9278954, 7.2)
Affinity DataIC50: 72nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212754BDBM212754(US9278954, 6.8 isomer 2 | US9278954, 7.34 | US9278...)
Affinity DataIC50: 75nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212615BDBM212615(US9278954, 1.9 | BDBM212741 | US9278954, 1.6)
Affinity DataIC50: 86nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212703BDBM212703(US9278954, 2.1)
Affinity DataIC50: 95nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212626BDBM212626(BDBM212745 | US9278954, 1.17)
Affinity DataIC50: 95nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212612BDBM212612(US9278954, 1.4 | US9278954, 1.3)
Affinity DataIC50: 101nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212822BDBM212822(US9278954, 8.1)
Affinity DataIC50: 104nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212612BDBM212612(US9278954, 1.4 | US9278954, 1.3)
Affinity DataIC50: 118nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212622BDBM212622(US9278954, 1.13 | BDBM212747 | US9278954, 1.26)
Affinity DataIC50: 121nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212636BDBM212636(US9278954, 1.27 | BDBM212752)
Affinity DataIC50: 126nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212622BDBM212622(US9278954, 1.13 | BDBM212747 | US9278954, 1.26)
Affinity DataIC50: 127nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212614BDBM212614(US9278954, 1.5)
Affinity DataIC50: 133nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212645BDBM212645(US9278954, 1.36 | BDBM212750)
Affinity DataIC50: 135nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212610BDBM212610(US9278954, 6.1 isomer 2 | US9278954, 6.1 isomer 1 ...)
Affinity DataIC50: 139nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212615BDBM212615(US9278954, 1.9 | BDBM212741 | US9278954, 1.6)
Affinity DataIC50: 140nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212616BDBM212616(US9278954, 1.7)
Affinity DataIC50: 170nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212615BDBM212615(US9278954, 1.9 | BDBM212741 | US9278954, 1.6)
Affinity DataIC50: 177nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212617BDBM212617(US9278954, 1.8)
Affinity DataIC50: 179nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212704BDBM212704(US9278954, 2.2)
Affinity DataIC50: 179nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212705BDBM212705(US9278954, 2.3)
Affinity DataIC50: 188nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212760BDBM212760(US9278954, 7.3)
Affinity DataIC50: 190nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212615BDBM212615(US9278954, 1.9 | BDBM212741 | US9278954, 1.6)
Affinity DataIC50: 195nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212619BDBM212619(US9278954, 1.12 | US9278954, 1.10)
Affinity DataIC50: 205nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212620BDBM212620(US9278954, 1.11)
Affinity DataIC50: 213nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212615BDBM212615(US9278954, 1.9 | BDBM212741 | US9278954, 1.6)
Affinity DataIC50: 219nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212619BDBM212619(US9278954, 1.12 | US9278954, 1.10)
Affinity DataIC50: 220nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212762BDBM212762(US9278954, 7.4)
Affinity DataIC50: 224nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212764BDBM212764(US9278954, 7.5)
Affinity DataIC50: 225nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212766BDBM212766(US9278954, 7.6)
Affinity DataIC50: 229nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212622BDBM212622(US9278954, 1.13 | BDBM212747 | US9278954, 1.26)
Affinity DataIC50: 233nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212713BDBM212713(US9278954, 3.1)
Affinity DataIC50: 235nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212623BDBM212623(US9278954, 1.22 | US9278954, 1.14)
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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212715BDBM212715(US9278954, 3.2)
Affinity DataIC50: 259nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212624BDBM212624(US9278954, 1.15)
Affinity DataIC50: 263nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212768BDBM212768(US9278954, 7.7)
Affinity DataIC50: 265nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212625BDBM212625(US9278954, 1.16)
Affinity DataIC50: 266nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212626BDBM212626(BDBM212745 | US9278954, 1.17)
Affinity DataIC50: 272nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212770BDBM212770(US9278954, 7.8)
Affinity DataIC50: 274nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212717BDBM212717(US9278954, 3.3)
Affinity DataIC50: 280nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212627BDBM212627(US9278954, 1.18)
Affinity DataIC50: 286nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212734BDBM212734(US9278954, 4.1)
Affinity DataIC50: 288nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212628BDBM212628(US9278954, 1.19)
Affinity DataIC50: 296nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212719BDBM212719(US9278954, 3.4)
Affinity DataIC50: 300nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212629BDBM212629(US9278954, 1.20)
Affinity DataIC50: 306nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212630BDBM212630(US9278954, 1.21)
Affinity DataIC50: 309nMpH: 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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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

US Patent
LigandChemical structure of BindingDB Monomer ID 212623BDBM212623(US9278954, 1.22 | US9278954, 1.14)
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
In Depth
Date in BDB:
2/13/2017
Entry Details
US Patent

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