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Found 176 with Last Name = 'bordeleau' and Initial = 'j'
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50005004(CHEMBL2397309)
Affinity DataIC50:  22nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175297(CHEMBL3810245)
Affinity DataIC50:  31nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50005008(CHEMBL2397312)
Affinity DataIC50:  35nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50005009(CHEMBL2397311)
Affinity DataIC50:  40nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50436476(CHEMBL2397316)
Affinity DataIC50:  48nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50436477(CHEMBL2397315)
Affinity DataIC50:  53nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50005007(CHEMBL2397310)
Affinity DataIC50:  53nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4-kinase beta(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50005010(CHEMBL2397313)
Affinity DataIC50:  67nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Boehringer Ingelheim

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

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

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

Curated by ChEMBL
LigandPNGBDBM50005011(CHEMBL2397303)
Affinity DataIC50:  100nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

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

Curated by ChEMBL
LigandPNGBDBM50005005(CHEMBL2397317)
Affinity DataIC50:  137nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

Curated by ChEMBL
LigandPNGBDBM50175302(CHEMBL3808401)
Affinity DataIC50:  150nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175303(CHEMBL3810042)
Affinity DataIC50:  180nMAssay Description:Inhibition of CYP2C8 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

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

Curated by ChEMBL
LigandPNGBDBM50061509((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)
Affinity DataIC50:  200nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

Curated by ChEMBL
LigandPNGBDBM50436478(CHEMBL2397314)
Affinity DataIC50:  225nMAssay Description:Inhibition of PI4K3beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

Curated by ChEMBL
LigandPNGBDBM50061497((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)
Affinity DataIC50:  300nMAssay Description:Activity against serine protease porcine pancreatic elastase (PPE)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

Curated by ChEMBL
LigandPNGBDBM50005011(CHEMBL2397303)
Affinity DataIC50:  500nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

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

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

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

Curated by ChEMBL
LigandPNGBDBM50436481(CHEMBL2397305)
Affinity DataIC50:  710nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

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

Curated by ChEMBL
LigandPNGBDBM50005006(CHEMBL2397307)
Affinity DataIC50:  980nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061551((S)-2-{(S)-2-[3-(4-Hydroxy-phenyl)-propionylamino]...)
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 ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061505((S)-2-[(S)-2-((S)-2-Acetylamino-3-methyl-butyrylam...)
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 ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061553((S)-2-[(S)-2-(3,3-Dimethyl-butyrylamino)-3,3-dimet...)
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 ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061510((S)-N*1*-(2-Benzothiazol-2-yl-1-methyl-2-oxo-ethyl...)
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 ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061498((S)-2-((S)-2-(3,3-dimethylbutanamido)-3,3-dimethyl...)
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 ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175303(CHEMBL3810042)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061540((S)-2-[(S)-3,3-Dimethyl-2-(3-methyl-butyrylamino)-...)
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 ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061534(4-{(S)-1-[(S)-2-Dimethylcarbamoyl-1-(3,3,3-trifluo...)
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 ArticlePubMed
TargetCytochrome P450 2C8(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175304(CHEMBL3808842)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of CYP2C8 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061526((S)-2-{(S)-2-[(S)-2-(2-Acetylamino-acetylamino)-3-...)
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 ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50436482(CHEMBL2397304)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175296(CHEMBL3809896)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Human rhinovirus B)
Boehringer Ingelheim

Curated by ChEMBL
LigandPNGBDBM50061538((S)-2-[(S)-2-((S)-2-Acetylamino-3-methyl-butyrylam...)
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 ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175296(CHEMBL3809896)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase 17A(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50436476(CHEMBL2397316)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of STK17A (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Boehringer Ingelheim (Canada)

Curated by ChEMBL
LigandPNGBDBM50175304(CHEMBL3808842)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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