Compile Data Set for Download or QSAR
Found 569 with Last Name = 'hu' and Initial = 'dx'
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538576(CHEMBL4634092)copy SMILEScopy InChI
Affinity DataIC50: 0.160nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538571(CHEMBL4635160)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538560(CHEMBL4640002)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538572(CHEMBL4649132)copy SMILEScopy InChI
Affinity DataIC50: 0.260nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538575(CHEMBL4638458)copy SMILEScopy InChI
Affinity DataIC50: 0.320nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538562(CHEMBL4643330)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538578(CHEMBL4640729)copy SMILEScopy InChI
Affinity DataIC50: 0.390nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538579(CHEMBL4647217)copy SMILEScopy InChI
Affinity DataIC50: 0.440nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM448932(5-Fluoro-4-(5-fluoro-1,1-dimethyl-2,3-dihydro-1H-b...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455061(CHEMBL4211828 | US10696678, Example 65)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538582(CHEMBL4638998)copy SMILEScopy InChI
Affinity DataIC50: 0.780nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455057(CHEMBL4215702 | US10696678, Example 20)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455050(CHEMBL4208172 | US10696678, Example 18 | US1135117...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of recombinant human full length CDK6 expressed in baculovirus infected Sf9 insect cells using histone H1 substrate after 90 mins by ADP-G...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455068(CHEMBL4205645 | US10696678, Example 22)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538563(CHEMBL4648116)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538570(CHEMBL4638573)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538564(CHEMBL4641569)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538583(CHEMBL4643112)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538567(CHEMBL4633860)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538577(CHEMBL4648623)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455051(CHEMBL4210028 | US10696678, Example 24)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50110183(Abemaciclib | LY-2835219 | US10626107, Example LY2...)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50110183(Abemaciclib | LY-2835219 | US10626107, Example LY2...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged CDK4 (S4 to E303 residues)/Cyclin D1 (Q4 to I295 residues) expressed in sf9 cells using Rb prot...More data for this Ligand-Target Pair
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591075(CHEMBL5200118)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538569(CHEMBL4644317)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455074(CHEMBL4217694 | US10696678, Example 67)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition of recombinant human full length CDK6 expressed in baculovirus infected Sf9 insect cells using histone H1 substrate after 90 mins by ADP-G...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538581(CHEMBL4642862)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591046(CHEMBL5202342)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538568(CHEMBL4640563)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM448932(5-Fluoro-4-(5-fluoro-1,1-dimethyl-2,3-dihydro-1H-b...)copy SMILEScopy InChI
Affinity DataIC50: 3.70nMAssay Description:Inhibition of recombinant human full length CDK6 expressed in baculovirus infected Sf9 insect cells using histone H1 substrate after 90 mins by ADP-G...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455057(CHEMBL4215702 | US10696678, Example 20)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of recombinant human full length CDK6 expressed in baculovirus infected Sf9 insect cells using histone H1 substrate after 90 mins by ADP-G...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetVasoactive intestinal polypeptide receptor 2(Homo sapiens (Human))TBA
LigandPNGBDBM50606528(CHEMBL5219662)copy SMILES
Affinity DataIC50: 4.5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9H5MPubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538565(CHEMBL4635798)copy SMILEScopy InChI
Affinity DataIC50: 4.60nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591045(CHEMBL5209076)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591054(CHEMBL5179922)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591066(CHEMBL5190023)copy SMILES
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455049(CHEMBL4209318 | US10696678, Example 63)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455048(CHEMBL4210707 | US10696678, Example 36)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetC-C chemokine receptor type 4(Homo sapiens (Human))
RAPT Therapeutics

Curated by ChEMBL
LigandPNGBDBM50545768(CHEMBL4641127)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Antagonist activity at human CCR4 expressed in rat chem-5 cells assessed as inhibition of CCL22-induced calcium flux measured at 2.5 secs time interv...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ0CW6PubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538574(CHEMBL4638688)copy SMILEScopy InChI
Affinity DataIC50: 6.60nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455058(CHEMBL4208366 | US10696678, Example 14)copy SMILEScopy InChI
Affinity DataIC50: 6.80nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50455050(CHEMBL4208172 | US10696678, Example 18 | US1135117...)copy SMILEScopy InChI
Affinity DataIC50: 7.40nMAssay Description:Inhibition of CDK4 (unknown origin) after 90 mins by ADP-Glo assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC4236PubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Beijing University of Technology

Curated by ChEMBL
LigandPNGBDBM50110183(Abemaciclib | LY-2835219 | US10626107, Example LY2...)copy SMILEScopy InChI
Affinity DataIC50: 7.80nMAssay Description:Inhibition of recombinant human full length CDK6 expressed in baculovirus infected Sf9 insect cells using histone H1 substrate after 90 mins by ADP-G...More data for this Ligand-Target Pair
TargeteIF-2-alpha kinase GCN2(Homo sapiens (Human))TBA
LigandPNGBDBM50591079(CHEMBL5196751)copy SMILES
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1PJSPubMed
TargetC-C chemokine receptor type 4(Homo sapiens (Human))
RAPT Therapeutics

Curated by ChEMBL
LigandPNGBDBM50545779(CHEMBL4642563)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Antagonist activity at human CCR4 expressed in rat chem-5 cells assessed as inhibition of CCL22-induced calcium flux measured at 2.5 secs time interv...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ0CW6PubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
RAPT Therapeutics, Inc.

Curated by ChEMBL
LigandPNGBDBM50538566(CHEMBL4632475)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of recombinant full length USP7 (unknown origin) using ubiquintin-rhodamine as substrate preincubated for 30 mins followed by substrate ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
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