Compile Data Set for Download or QSAR
Found 127 Enz. Inhib. hit(s) with Target = 'Ubiquitin carboxyl-terminal hydrolase 5'
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50437693(VIALININ A)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of wild type human USP5 expressed in Escherichia coli BL21(DE3) using Ub-AMC as substrate after 60 mins by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15528PubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50437693(VIALININ A)copy SMILEScopy InChI
Affinity DataKi:  1.25E+4nMAssay Description:Competitive inhibition of wild type human USP5 expressed in Escherichia coli BL21(DE3) using Ub-AMC as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15528PubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50326016(3-amino-2-benzoyl-6-oxo-6,7-dihydrothieno[2,3-b]py...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+5nMAssay Description:Inhibition of isopeptidase TMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KW5G7PPubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50412352(CHEMBL5278336)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of AChE in organophosphate-susceptible clone of Schizaphis graminum OSS adult or last-instar nymphs homogenates assessed as bimolecular ra...More data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50437695(CHEMBL1923233)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of USP5 in human Z138 cells after 1 hr by immunoblotting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15528PubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50437693(VIALININ A)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of wild type human USP5 expressed in Escherichia coli BL21(DE3) using Ub-AMC as substrate after 60 mins by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15528PubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50412352(CHEMBL5278336)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of AChE in organophosphate-resistant clone of Schizaphis graminum OR1 adult or last-instar nymphs homogenates assessed as bimolecular rate...More data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50538571(CHEMBL4635160)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human 6His-tagged USP5 expressed in Escherichia coli assessed as cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine1...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XK8K2TPubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50608542(CHEMBL5276142)copy SMILES
Affinity DataIC50: 2.15E+4nMMore data for this Ligand-Target Pair
Ligand InfoPDB
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50412352(CHEMBL5278336)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of AChE in organophosphate-susceptible clone of Schizaphis graminum OSS adult or last-instar nymphs homogenates assessed as bimolecular ra...More data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50608541(CHEMBL1493046)copy SMILES
Affinity DataIC50: 2.91E+4nMMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50412352(CHEMBL5278336)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of AChE in organophosphate-resistant clone of Schizaphis graminum OR1 adult or last-instar nymphs homogenates assessed as bimolecular rate...More data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50437694(CHEMBL1410015)copy SMILEScopy InChI
Affinity DataIC50: 1.43E+5nMMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50271098(CHEMBL4129140)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+5nMAssay Description:Inhibition of USP5 (unknown origin) using Ub-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by fluor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5WVGPubMed
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50608424(CHEMBL5267683)copy SMILES
Affinity DataIC50: 2.00E+5nMMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411310(CHEMBL5273690)copy SMILEScopy InChI
Affinity DataKd:  9.40E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411330(CHEMBL5282333)copy SMILEScopy InChI
Affinity DataKd:  1.50E+5nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411331(CHEMBL5270273)copy SMILEScopy InChI
Affinity DataKd:  5.40E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411332(CHEMBL5270844)copy SMILEScopy InChI
Affinity DataKd:  9.00E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411349(CHEMBL5285781)copy SMILEScopy InChI
Affinity DataKd:  9.20E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411350(CHEMBL5283991)copy SMILEScopy InChI
Affinity DataKd:  8.70E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411351(CHEMBL5290299)copy SMILEScopy InChI
Affinity DataKd:  6.10E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411352(CHEMBL5285743)copy SMILEScopy InChI
Affinity DataKd:  1.30E+5nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411353(CHEMBL5274321)copy SMILEScopy InChI
Affinity DataKd:  2.20E+5nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411354(CHEMBL5273898)copy SMILEScopy InChI
Affinity DataKd:  8.00E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411355(CHEMBL5282155)copy SMILEScopy InChI
Affinity DataKd:  3.80E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411357(CHEMBL5290717)copy SMILEScopy InChI
Affinity DataKd:  4.50E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411358(CHEMBL5268053)copy SMILEScopy InChI
Affinity DataKd:  3.40E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411359(CHEMBL5284407)copy SMILEScopy InChI
Affinity DataKd:  1.50E+5nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411360(CHEMBL5268432)copy SMILEScopy InChI
Affinity DataKd:  2.50E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411363(CHEMBL5277702)copy SMILEScopy InChI
Affinity DataKd:  1.90E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411432(CHEMBL5266727)copy SMILEScopy InChI
Affinity DataKd:  4.00E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411433(CHEMBL5285627)copy SMILEScopy InChI
Affinity DataKd:  2.30E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411434(CHEMBL5281654)copy SMILEScopy InChI
Affinity DataKd:  2.10E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411438(CHEMBL5265979)copy SMILEScopy InChI
Affinity DataKd:  2.20E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411440(CHEMBL5274675)copy SMILEScopy InChI
Affinity DataKd:  7.90E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411561(CHEMBL5266393)copy SMILEScopy InChI
Affinity DataKd:  1.80E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411964(CHEMBL5290467)copy SMILEScopy InChI
Affinity DataKd:  3.90E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411965(CHEMBL5269269)copy SMILEScopy InChI
Affinity DataKd:  3.10E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411968(CHEMBL5268349)copy SMILEScopy InChI
Affinity DataKd:  8.20E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411969(CHEMBL5290098)copy SMILEScopy InChI
Affinity DataKd:  4.20E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411970(CHEMBL5286035)copy SMILEScopy InChI
Affinity DataKd:  4.70E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411971(CHEMBL5289065)copy SMILEScopy InChI
Affinity DataKd:  5.90E+4nMAssay Description:Inhibition of carbonic anhydrase 2 assessed as inhibition of carbon dioxide hydrationMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411972(CHEMBL5271929)copy SMILEScopy InChI
Affinity DataKd:  9.00E+3nMAssay Description:Binding affinity to human CD69 receptor expressed in Escherichia coli by equilibrium dialysisMore data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411973(CHEMBL5286558)copy SMILEScopy InChI
Affinity DataKd:  2.10E+5nMAssay Description:Binding affinity to human monomeric CD69 receptor expressed in Escherichia coli by equilibrium dialysisMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411974(CHEMBL5288864)copy SMILEScopy InChI
Affinity DataKd: >1.00E+6nMAssay Description:Binding affinity to human dimeric CD69 receptor expressed in Escherichia coli by equilibrium dialysisMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411975(CHEMBL5270943)copy SMILEScopy InChI
Affinity DataKd:  7.00E+3nMAssay Description:Inhibition of Manduca sexta V-ATPase V1/Vo holoenzyme activity assessed as inorganic phosphate production pretreated for 5 minsMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411976(CHEMBL5273795)copy SMILEScopy InChI
Affinity DataKd:  2.20E+4nMAssay Description:Inhibition of Manduca sexta V-ATPase V1/Vo holoenzyme activity assessed as inorganic phosphate production pretreated for 5 minsMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50411977(CHEMBL5280865)copy SMILEScopy InChI
Affinity DataKd:  2.10E+4nMAssay Description:Inhibition of Manduca sexta V-ATPase V1/Vo holoenzyme activity assessed as inorganic phosphate production pretreated for 5 minsMore data for this Ligand-Target Pair
In DepthDetails
TargetUbiquitin carboxyl-terminal hydrolase 5(Homo sapiens (Human))
Tokyo University of Agriculture

Curated by ChEMBL
LigandPNGBDBM50412084(CHEMBL5282742)copy SMILEScopy InChI
Affinity DataKd:  6.10E+4nMAssay Description:Inhibition of Manduca sexta V-ATPase V1/Vo holoenzyme activity assessed as inorganic phosphate production pretreated for 5 minsMore data for this Ligand-Target Pair
In DepthDetails
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