Compile Data Set for Download or QSAR
Report error Found 38 Enz. Inhib. hit(s) with all data for entry = 50023453
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50648642BDBM50648642(CHEMBL5611924)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50648639BDBM50648639(CHEMBL5614311)
Affinity DataIC50: 1.60nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50648643BDBM50648643(CHEMBL5612048)
Affinity DataIC50: 2.30nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Rat)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663885BDBM50663885(CHEMBL6163544)
Affinity DataIC50: 3nMAssay Description:Inhibition of recombinant His-tagged rat KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663874BDBM50663874(CHEMBL6174745)
Affinity DataIC50: 3.20nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663866BDBM50663866(CHEMBL6170657)
Affinity DataIC50: 4.20nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663875BDBM50663875(CHEMBL6163124)
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663867BDBM50663867(CHEMBL6163060)
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663865BDBM50663865(CHEMBL6148712)
Affinity DataIC50: 5.5nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663879BDBM50663879(CHEMBL6164595)
Affinity DataIC50: 5.70nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663869BDBM50663869(CHEMBL6162778)
Affinity DataIC50: 5.80nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663878BDBM50663878(CHEMBL6164870)
Affinity DataIC50: 7.40nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663876BDBM50663876(CHEMBL6172297)
Affinity DataIC50: 7.5nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663881BDBM50663881(CHEMBL6166586)
Affinity DataIC50: 9.40nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663864BDBM50663864(CHEMBL6167999)
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663860BDBM50663860(CHEMBL6173466)
Affinity DataIC50: 11nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663885BDBM50663885(CHEMBL6163544)
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant His-tagged human KHK-A using D-fructose as substrate incubated for 60 mins by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663868BDBM50663868(CHEMBL6162143)
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663877BDBM50663877(CHEMBL6145649)
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663885BDBM50663885(CHEMBL6163544)
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand InfoPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663882BDBM50663882(CHEMBL6175032)
Affinity DataIC50: 13nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663862BDBM50663862(CHEMBL6152491)
Affinity DataIC50: 18nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663870BDBM50663870(CHEMBL6152490)
Affinity DataIC50: 19nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663883BDBM50663883(CHEMBL6167877)
Affinity DataIC50: 19nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663861BDBM50663861(CHEMBL6162192)
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663859BDBM50663859(CHEMBL6167828)
Affinity DataIC50: 23nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663884BDBM50663884(CHEMBL5315520)
Affinity DataIC50: 25nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663880BDBM50663880(CHEMBL6143992)
Affinity DataIC50: 27nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663880BDBM50663880(CHEMBL6143992)
Affinity DataIC50: 27nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663873BDBM50663873(CHEMBL6149929)
Affinity DataIC50: 31nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663863BDBM50663863(CHEMBL6175208)
Affinity DataIC50: 33nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663880BDBM50663880(CHEMBL6143992)
Affinity DataIC50: 40nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Mouse)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663885BDBM50663885(CHEMBL6163544)
Affinity DataIC50: 59nMAssay Description:Inhibition of KHK in mouse hepatocytes using D-fructose as substrate assessed as reduction in fructose-1-phosphate level preincubated for 30 mins fol...More data for this Ligand-Target Pair
Ligand InfoPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663871BDBM50663871(CHEMBL6170029)
Affinity DataIC50: 63nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50241178BDBM50241178(CHEMBL4070442)
Affinity DataIC50: 187nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663872BDBM50663872(CHEMBL6170017)
Affinity DataIC50: 705nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Human)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663886BDBM50663886(CHEMBL5315603)
Affinity DataIC50: 5.03E+3nMAssay Description:Inhibition of recombinant His-tagged human KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetKetohexokinase(Rat)
Boehringer Ingelheim Pharma GmbH & Co. KG

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50663886BDBM50663886(CHEMBL5315603)
Affinity DataIC50: 8.87E+3nMAssay Description:Inhibition of recombinant His-tagged rat KHK-C using D-fructose as substrate incubated for 60 mins in presence of ATP by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed