Compile Data Set for Download or QSAR
maximum 50k data
Found 57 with Last Name = 'barker' and Initial = 'o'
TargetProtein kinase C alpha type(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM2579((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human PKCalpha activity using kemptide as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465231(CHEMBL4288150 | US10766903, Example 30)
Affinity DataIC50:  6nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465234(CHEMBL4283787 | US10766903, Example 46)
Affinity DataIC50:  22nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465202(CHEMBL4290015 | US10766903, Example 29)
Affinity DataIC50:  24nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465229(CHEMBL4283226 | US10766903, Example 27)
Affinity DataIC50:  30nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465203(CHEMBL4281720 | US10766903, Example 28)
Affinity DataIC50:  30nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit beta(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM2579((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)
Affinity DataIC50:  33nMAssay Description:Inhibition of PKA activity using neurogranin as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465236(CHEMBL4291074 | US10766903, Example 25)
Affinity DataIC50:  35nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465230(CHEMBL4289604 | US10766903, Example 104)
Affinity DataIC50:  39nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465205(CHEMBL4287721 | US10766903, Example 107)
Affinity DataIC50:  40nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465237(CHEMBL4279817 | US10766903, Example 106)
Affinity DataIC50:  50nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465195(CHEMBL4294967)
Affinity DataIC50:  75nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465213(CHEMBL4294359 | US10766903, Example 11)
Affinity DataIC50:  90nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465200(CHEMBL4282783 | US10766903, Example 97)
Affinity DataIC50:  90nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50342212(1-[1-(3-Dimethylaminopropyl)-1H-indol-3-yl]-3-(4-p...)
Affinity DataIC50:  95nMAssay Description:Inhibition of human PKCalpha activity using kemptide as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465210(CHEMBL4290969 | US10766903, Example 6)
Affinity DataIC50:  120nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465198(CHEMBL4279330 | US10766903, Example 98)
Affinity DataIC50:  150nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465225(CHEMBL4292475 | US10766903, Example 22)
Affinity DataIC50:  240nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465204(CHEMBL4284325 | US10766903, Example 108)
Affinity DataIC50:  250nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465224(CHEMBL4285285 | US10766903, Example 21)
Affinity DataIC50:  300nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465235(CHEMBL4281848 | US10766903, Example 24)
Affinity DataIC50:  300nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465228(CHEMBL4287739)
Affinity DataIC50:  300nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465242(CHEMBL4294482 | US10766903, Example 32)
Affinity DataIC50:  330nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465233(CHEMBL4287543 | US10766903, Example 7)
Affinity DataIC50:  390nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465199(CHEMBL4286591 | US10766903, Example 33)
Affinity DataIC50:  560nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465212(CHEMBL4287139)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465201(CHEMBL4284493 | US10766903, Example 99)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465211(CHEMBL4292144)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465232(CHEMBL4280922 | US10766903, Example 4)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465214(CHEMBL4286062)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50342213(1-[1-(3-Diethylaminopropyl)-1H-indol-3-yl]-3-(6-ph...)
Affinity DataIC50:  2.69E+3nMAssay Description:Inhibition of human PKCalpha activity using kemptide as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465209(CHEMBL4279391 | US10766903, Example 116)
Affinity DataIC50:  2.80E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465207(CHEMBL4291560)
Affinity DataIC50:  4.20E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50342214(1-[1-(3-Diethylaminopropyl)-1H-indol-3-yl]-3-(2-ph...)
Affinity DataIC50:  4.81E+3nMAssay Description:Inhibition of human PKCalpha activity using kemptide as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465238(CHEMBL4280334 | US10766903, Example 10)
Affinity DataIC50:  7.20E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465241(CHEMBL4280723)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50342215(1-[1-(3-Diethylaminopropyl)-1H-indol-3-yl]-3-(6-ph...)
Affinity DataIC50:  8.07E+3nMAssay Description:Inhibition of human PKCalpha activity using kemptide as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465223(CHEMBL4288626)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465196(CHEMBL4276901 | US10766903, Example 109)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465222(CHEMBL4284163)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465227(CHEMBL4292042)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465218(CHEMBL4291148)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465206(CHEMBL4277510 | US10766903, Example 67)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-dependent protein kinase catalytic subunit beta(Homo sapiens (Human))
Procter & Gamble Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50342212(1-[1-(3-Dimethylaminopropyl)-1H-indol-3-yl]-3-(4-p...)
Affinity DataIC50:  2.36E+4nMAssay Description:Inhibition of PKA activity using neurogranin as a substrate in presence of 50 uM ATP by mass spectrometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465216(CHEMBL4282043)
Affinity DataIC50:  3.20E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465221(CHEMBL4276903)
Affinity DataIC50:  3.40E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465239(CHEMBL4284337 | US10766903, Example 38)
Affinity DataIC50:  4.40E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465217(CHEMBL4280518)
Affinity DataIC50:  4.60E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465220(CHEMBL4287544)
Affinity DataIC50:  6.00E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Almac Discovery

Curated by ChEMBL
LigandPNGBDBM50465219(CHEMBL4288834)
Affinity DataIC50:  7.80E+4nMAssay Description:Inhibition of USP7 (unknown origin) by biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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