Compile Data Set for Download or QSAR
Report error Found 104 Enz. Inhib. hit(s) with all data for entry = 50017279
TargetBile acid receptor(Mouse)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  14nMAssay Description:Agonist activity at mouse LBD fused FXR in HEK293 cells incubated for 30 min by envision plate reader methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600732BDBM50600732(CHEMBL5202191)
Affinity DataEC50:  25nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600719BDBM50600719(CHEMBL5181899)
Affinity DataEC50:  25nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600713BDBM50600713(CHEMBL5187016)
Affinity DataEC50:  27nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538277BDBM538277(US11254663, Example 119)
Affinity DataEC50:  29nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  34nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600727BDBM50600727(CHEMBL5177647)
Affinity DataEC50:  41nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  42nMAssay Description:Agonist activity at LBD fused human FXR in HEK293 cells incubated for 30 min by envision plate reader methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600720BDBM50600720(CHEMBL5189418)
Affinity DataEC50:  44nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538299BDBM538299(US11254663, Example 157)
Affinity DataEC50:  45nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  53nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600712BDBM50600712(CHEMBL5169696)
Affinity DataEC50:  57nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600716BDBM50600716(CHEMBL5174333)
Affinity DataEC50:  59nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600706BDBM50600706(CHEMBL5190997)
Affinity DataEC50:  66nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600726BDBM50600726(CHEMBL5172239)
Affinity DataEC50:  70nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  84nMAssay Description:Agonist activity at human FXR2 expressed in HEK293 cells coexpressing IBABPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  85nMAssay Description:Agonist activity at human FXR2 expressed in HEK293 cells coexpressing IBABPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600714BDBM50600714(CHEMBL5174082)
Affinity DataEC50:  92nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600725BDBM50600725(CHEMBL5180682)
Affinity DataEC50:  93nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600715BDBM50600715(CHEMBL5178176)
Affinity DataEC50:  95nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538513BDBM538513(US11254663, Example 440)
Affinity DataEC50:  104nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600711BDBM50600711(CHEMBL5203086)
Affinity DataEC50:  111nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600730BDBM50600730(CHEMBL5173549)
Affinity DataEC50:  111nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600724BDBM50600724(CHEMBL5199184)
Affinity DataEC50:  114nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600709BDBM50600709(CHEMBL5184707)
Affinity DataEC50:  118nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600710BDBM50600710(CHEMBL5196639)
Affinity DataEC50:  142nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600721BDBM50600721(CHEMBL5184419)
Affinity DataEC50:  149nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  150nMAssay Description:Agonist activity at human FXR2 expressed in HEK293 cells coexpressing human FGF19 incubated for 24 hrs by ELISA analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600731BDBM50600731(CHEMBL5178315)
Affinity DataEC50:  152nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600707BDBM50600707(CHEMBL5205123)
Affinity DataEC50:  152nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600728BDBM50600728(CHEMBL5189617)
Affinity DataEC50:  170nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  191nMAssay Description:Agonist activity at human FXR2 expressed in HEK293 cells coexpressing human FGF19 incubated for 24 hrs by ELISA analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538213BDBM538213(US11254663, Example 10)
Affinity DataEC50:  228nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600729BDBM50600729(CHEMBL5208567)
Affinity DataEC50:  232nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  243nMAssay Description:Agonist activity at human FXR2 expressed in Huh-7 cells coexpressing BSEPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  281nMAssay Description:Agonist activity at human FXR2 expressed in Huh-7 cells coexpressing BSEP relative to GW2064More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600708BDBM50600708(CHEMBL5191475)
Affinity DataEC50:  299nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C19(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600721BDBM50600721(CHEMBL5184419)
Affinity DataIC50: 300nMAssay Description:Inhibition of recombinant CYP2C19 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Mouse)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  320nMAssay Description:Agonist activity at mouse LBD fused FXR in HEK293 cells incubated for 30 min by envision plate reader methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50572221BDBM50572221(CHEMBL4862974)
Affinity DataEC50:  351nMAssay Description:Agonist activity at LBD fused human FXR in HEK293 cells incubated for 30 min by envision plate reader methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetRNA-binding protein FXR2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600733BDBM50600733(CHEMBL5182534)
Affinity DataEC50:  389nMAssay Description:Agonist activity at human FXR2 expressed in Huh-7 cells coexpressing BSEPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600717BDBM50600717(CHEMBL5204574)
Affinity DataEC50:  538nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetBile acid receptor(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600718BDBM50600718(CHEMBL5201654)
Affinity DataEC50:  919nMAssay Description:Agonist activity at Gal4-fused human FXR in HEK293 cells incubated for 15 min by luciferase reporter assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C19(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538299BDBM538299(US11254663, Example 157)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C19 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C9(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600727BDBM50600727(CHEMBL5177647)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C9 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hrs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C9(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600731BDBM50600731(CHEMBL5178315)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C9 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hrs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C9(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600730BDBM50600730(CHEMBL5173549)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C9 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hrs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C9(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 538213BDBM538213(US11254663, Example 10)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C9 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hrs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetNuclear receptor subfamily 1 group I member 2(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600725BDBM50600725(CHEMBL5180682)
Affinity DataEC50:  1.00E+3nMAssay Description:Transactivation of PXR (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
TargetCytochrome P450 2C9(Human)
Biocon-Bristol Myers Squibb Research and Development Center

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50600724BDBM50600724(CHEMBL5199184)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of recombinant CYP2C9 (unknown origin) using fluorogenic substrate preincubated for 15 min followed by NADPH addition measured after 2 hrs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2023
Entry Details
PubMed
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