Compile Data Set for Download or QSAR
Found 176 with Last Name = 'bordeleau' and Initial = 'j'
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005004(CHEMBL2397309)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175297(CHEMBL3810245)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005008(CHEMBL2397312)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005009(CHEMBL2397311)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436476(CHEMBL2397316)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436477(CHEMBL2397315)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005007(CHEMBL2397310)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005010(CHEMBL2397313)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061511((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061512((S)-N*1*-(2-Benzooxazol-2-yl-1-methyl-2-oxo-ethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061532((S)-N*1*-{2-[(Benzo[1,3]dioxol-5-ylmethyl)-carbamo...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005011(CHEMBL2397303)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061537((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061518((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005005(CHEMBL2397317)copy SMILEScopy InChI
Affinity DataIC50: 137nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061515((S)-N*1*-[2-(2-Benzyloxy-ethylcarbamoyl)-1-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175302(CHEMBL3808401)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175303(CHEMBL3810042)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of CYP2C8 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061503((S)-N*1*-(2-Benzylcarbamoyl-1-methyl-2-oxo-ethyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061528((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061509((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061506((S)-N*1*-{2-[(1H-Benzoimidazol-2-ylmethyl)-carbamo...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436478(CHEMBL2397314)copy SMILEScopy InChI
Affinity DataIC50: 225nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061544((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061497((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061530((S)-N*1*-((S)-3-Benzylcarbamoyl-3,3-difluoro-1-met...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005011(CHEMBL2397303)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061512((S)-N*1*-(2-Benzooxazol-2-yl-1-methyl-2-oxo-ethyl)...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061509((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061528((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061516((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436481(CHEMBL2397305)copy SMILEScopy InChI
Affinity DataIC50: 710nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061511((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50005006(CHEMBL2397307)copy SMILEScopy InChI
Affinity DataIC50: 980nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061551((S)-2-{(S)-2-[3-(4-Hydroxy-phenyl)-propionylamino]...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061505((S)-2-[(S)-2-((S)-2-Acetylamino-3-methyl-butyrylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061553((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061510((S)-N*1*-(2-Benzothiazol-2-yl-1-methyl-2-oxo-ethyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061498((S)-2-((S)-2-(3,3-dimethylbutanamido)-3,3-dimethyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175303(CHEMBL3810042)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061540((S)-2-[(S)-3,3-Dimethyl-2-(3-methyl-butyrylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061534(4-{(S)-1-[(S)-2-Dimethylcarbamoyl-1-(3,3,3-trifluo...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175304(CHEMBL3808842)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of CYP2C8 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061526((S)-2-{(S)-2-[(S)-2-(2-Acetylamino-acetylamino)-3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436482(CHEMBL2397304)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175296(CHEMBL3809896)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim Ltd.

Curated by ChEMBL
LigandPNGBDBM50061538((S)-2-[(S)-2-((S)-2-Acetylamino-3-methyl-butyrylam...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Micro molar potency of the compound to inhibit human cytomegalovirus (HCMV) proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC31HWPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175296(CHEMBL3809896)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
TargetSerine/threonine-protein kinase 17A(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50436476(CHEMBL2397316)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of STK17A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QCXPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada) Ltd.

Curated by ChEMBL
LigandPNGBDBM50175304(CHEMBL3808842)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B337TPubMed
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