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Found 126 with Last Name = 'boisclair' and Initial = 'md'
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)
Affinity DataIC50:  200nMAssay Description:Inhibition of Cyclin-dependent kinase 1-cyclin B1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)
Affinity DataIC50:  200nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088615(2-(4-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  550nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088606(2-(2-Bromo-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,3...)
Affinity DataIC50:  650nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50451015(CHEMBL9052)
Affinity DataIC50:  800nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088612(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  800nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088606(2-(2-Bromo-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,3...)
Affinity DataIC50:  980nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50451018(CHEMBL8675)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088612(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088608(2-(2,4-Dichloro-phenyl)-5,7-dihydroxy-8-(1-methyl-...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088610(2-(3-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088608(2-(2,4-Dichloro-phenyl)-5,7-dihydroxy-8-(1-methyl-...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088615(2-(4-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibitory activity against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088619(2-(2-Fluoro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088619(2-(2-Fluoro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088610(2-(3-Chloro-phenyl)-5,7-dihydroxy-8-(1-methyl-1,2,...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50451019(CHEMBL269124)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289899(CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...)
Affinity DataIC50:  3.80E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  4.20E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  4.20E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289899(CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...)
Affinity DataIC50:  4.60E+3nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286608(CHEMBL60072 | Sulfircin analogue | Sulfuric acid m...)
Affinity DataIC50:  4.70E+3nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289899(CHEMBL292556 | Sulfuric acid mono-[5-phenyl-1-((1S...)
Affinity DataIC50:  5.40E+3nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289906(2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...)
Affinity DataIC50:  5.60E+3nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289906(2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...)
Affinity DataIC50:  6.30E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50451014(CHEMBL8815)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibitory activity against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286608(CHEMBL60072 | Sulfircin analogue | Sulfuric acid m...)
Affinity DataIC50:  7.80E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289897(CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...)
Affinity DataIC50:  7.90E+3nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088607(4-[2-(2-Chloro-phenyl)-5,7-dihydroxy-4-oxo-4H-chro...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289897(CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...)
Affinity DataIC50:  8.40E+3nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289902(2-[3-Oxo-3-phenyl-1-((4aS,8aS)-2,5,5,8a-tetramethy...)
Affinity DataIC50:  8.60E+3nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088607(4-[2-(2-Chloro-phenyl)-5,7-dihydroxy-4-oxo-4H-chro...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  1.08E+4nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  1.08E+4nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  1.10E+4nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289900(CHEMBL303581 | Sulfuric acid mono-[5-furan-3-yl-1-...)
Affinity DataIC50:  1.10E+4nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50088614(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-((S)-2-hydroxy...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibitory activity against Cyclin-dependent kinase 1-cyclin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289903(CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...)
Affinity DataIC50:  1.65E+4nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289903(CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...)
Affinity DataIC50:  1.65E+4nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289897(CHEMBL60297 | Sulfuric acid mono-[5-furan-3-yl-2-m...)
Affinity DataIC50:  1.70E+4nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289906(2-[3-Phenyl-1-((1S,2S,4aS,8aR)-2,5,5,8a-tetramethy...)
Affinity DataIC50:  2.10E+4nMAssay Description:Concentration required for its inhibitory activity against PTB1B phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50088609(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-pyridin-4-yl-c...)
Affinity DataIC50:  2.10E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50088609(2-(2-Chloro-phenyl)-5,7-dihydroxy-8-pyridin-4-yl-c...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Mitotix

Curated by ChEMBL
LigandPNGBDBM50451020(CHEMBL8620)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibitory activity against cyclin-dependent kinase 4-cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289903(CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...)
Affinity DataIC50:  2.55E+4nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289903(CHEMBL64690 | Sulfuric acid mono-[3-phenyl-1-((1S,...)
Affinity DataIC50:  2.55E+4nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289904(CHEMBL62224 | Sulfuric acid mono-[1-benzyl-2-((1S,...)
Affinity DataIC50:  2.80E+4nMAssay Description:Concentration required for its inhibitory activity against VHR phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289904(CHEMBL62224 | Sulfuric acid mono-[1-benzyl-2-((1S,...)
Affinity DataIC50:  2.90E+4nMAssay Description:Concentration required for its inhibitory activity against Cdc25A phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
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