Compile Data Set for Download or QSAR
Report error Found 24 of affinity data for UniProtKB/TrEMBL: Q9JKB1
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53421(4-Cyclohexyl-2-phenyl-quinazoline | 4-cyclohexyl-2...)
Affinity DataIC50: 600nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53469(N-[1-(4-bromophenyl)ethylideneamino]-2-methyl-6-pi...)
Affinity DataIC50: 1.60E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53467(1,3-dimethyl-5-nitro-6-[(E)-2-(4-propoxyphenyl)vin...)
Affinity DataIC50: 1.70E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53470(2-N,2-N,4-N,4-N-tetraethyl-6-N-(4-nitrophenyl)-1,3...)
Affinity DataIC50: 1.80E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53443(N-[2-[(3-chlorobenzyl)thio]ethyl]-2-(3-chloro-N-me...)
Affinity DataIC50: 2.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53468(2-[[3-cyano-4-(2-methoxyphenyl)-6-phenyl-2-pyridin...)
Affinity DataIC50: 2.30E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53416(SMR000465882 | MLS000849591 | (2S)-2-[[4-[(4-chlor...)
Affinity DataIC50: 2.40E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53441(N-(1H-benzimidazol-2-yl)-3-chloranyl-benzamide | N...)
Affinity DataIC50: 2.50E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53442(1-[(7-chloro-3,5-dimethyl-1-benzofuran-2-yl)carbon...)
Affinity DataIC50: 2.50E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53413((2S)-6-(tert-butoxycarbonylamino)-2-[[4-(p-tolylca...)
Affinity DataIC50: 3.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53449(cid_1724426 | 4-(4-bromophenyl)-2-[(2-methylbenzoy...)
Affinity DataIC50: 3.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53414(benzyl (2S)-4-methyl-2-[[4-[(3-methylphenyl)carbam...)
Affinity DataIC50: 3.30E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53445(ethyl 2-[(4-hydroxy-3-nitrophenyl)methylidene]-5-(...)
Affinity DataIC50: 4.00E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53482(MLS001202596 | 1-butyl-N-[(2-chlorophenyl)methyl]-...)
Affinity DataIC50: 4.10E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53422(2,4-Dicyclohexyl-6-methoxy-quinazoline | 2,4-dicyc...)
Affinity DataIC50: 4.70E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53447(MLS001162917 | 4,4'-[1,4-phenylenebis(oxy)]dip...)
Affinity DataIC50: 4.70E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53419((2S)-2-[[4-[(4-methoxyphenyl)carbamoyl]-1H-imidazo...)
Affinity DataIC50: 4.80E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53454(SMR000516541 | (2E)-2-[(2Z)-2-(3-methoxy-4-oxo-1-c...)
Affinity DataIC50: 5.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53415(tert-butyl (2S)-2-[[4-[(3-methylphenyl)carbamoyl]-...)
Affinity DataIC50: 5.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53418((2S)-2-[[[4-[(4-chloroanilino)-oxomethyl]-1H-imida...)
Affinity DataIC50: 5.80E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM24778(Vitamin K3 | cid_4055 | 2-methyl-1,4-dihydronaphth...)
Affinity DataIC50: 7.10E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53471((3-ethyl-5-hydroxy-5-phenyl-4H-pyrazol-1-yl)-(2-hy...)
Affinity DataIC50: 7.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53448(1-methyl-1-[4-(4-methylphenyl)-6-phenylpyrimidin-2...)
Affinity DataIC50: 1.13E+5nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mouse)
Brigham and Women'S Hospital

LigandPNGBDBM53420(cid_16759673 | (4S,5S,6R)-6-methyl-2-oxo-4-(2-phen...)
Affinity DataIC50: 1.16E+5nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed