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Report error Found 68 of ic50 data for polymerid = 2395,4691
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50590284(CHEMBL5192316)
Affinity DataIC50: 10nMAssay Description:Inhibition of GST-tagged recombinant UCHL3 (unknown origin) using Ub-Lys-TAMRA as substrate incubated for 30 mins by fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50590283(CHEMBL5169766 | US20230303547, Reference Example D...)
Affinity DataIC50: 10nMAssay Description:Inhibition of GST-tagged recombinant UCHL3 (unknown origin) using Ub-Lys-TAMRA as substrate incubated for 30 mins by fluorescence polarization assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50431630(KRX-0401 | PERIFOSINE)
Affinity DataIC50: 50nMAssay Description:Inhibition of UCHL3 (unknown origin) assessed as reduction in RAD51 deubiquitination incubated for 4 hrsMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50594731(CHEMBL1241028)
Affinity DataIC50: 600nMAssay Description:Inhibition of recombinant human UCHL3 expressed in baculovirus infected Sf9 cells using ubiquitin-AMC as substrate preincubated for 30 mins followed ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM53421(4-Cyclohexyl-2-phenyl-quinazoline | 4-cyclohexyl-2...)
Affinity DataIC50: 600nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50069764(CHEMBL3407501)
Affinity DataIC50: 2.16E+3nMAssay Description:Inhibition of UCHL3 (unknown origin) using ubiquitin-AMC as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50594730(CHEMBL5193983)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of UCHL3 (unknown origin) incubated for 20 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50594729(CHEBI:27485 | CHEMBL1397260)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of UCHL3 (unknown origin) using Ub-AMC as substrate preincubated for 30 mins followed by substrate addition by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50538571(CHEMBL4635160)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human GST-tagged UCHL3 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
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM65518(LDN-57444 | 668467-91-2 | 5-Chloro-1-[(2,5-dichlor...)
Affinity DataIC50: 1.41E+4nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50442907(CHEMBL3039433 | Acetyl Isogambogic Acid)
Affinity DataIC50: 1.54E+4nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...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
Ligand InfoPC cidPC sid
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(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326012(3-(acetoxyimino)-5-bromo-1-(3,4-dichlorobenzyl)ind...)
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore 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(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326014(3-(acetoxyimino)-1-(3,4-dichlorobenzyl)-5-iodoindo...)
Affinity DataIC50: 2.30E+4nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore 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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM200235(Rifampicin | cid_5381226)
Affinity DataIC50: 2.48E+4nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326013(3-(acetoxyimino)-5-bromo-1-(2,5-dichlorobenzyl)ind...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50594733(CHEMBL4303698)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of UCHL3 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
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
Ligand InfoPC cidPC sid
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

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

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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM205457(Celastrol | (2R,4aS,6aR,6aS,14aS,14bR)-10-hydroxy-...)
Affinity DataIC50: 3.21E+4nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...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
Ligand InfoPC cidPC sid
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(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50594732(CHEMBL5195092)
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition of recombinant human UCHL3 expressed in baculovirus infected Sf9 cells using ubiquitin-AMC as substrate preincubated for 30 mins followed ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
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

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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50326015(5-(4-butylphenyl)-4-(4-isopropylphenyl)-4H-1,2,4-t...)
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore 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
Ligand InfoPC cidPC sid
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
Ligand InfoPC cidPC sid
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(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50242207(Mangiferin | CHEMBL455364)
Affinity DataIC50: 5.26E+4nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM24778(Vitamin K3 | cid_4055 | 2-methyl-1,4-dihydronaphth...)
Affinity DataIC50: 7.10E+4nMAssay Description:Inhibition of recombinant human UCHL3 expressed in baculovirus infected Sf9 cells using ubiquitin-AMC as substrate preincubated for 30 mins followed ...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM24778(Vitamin K3 | cid_4055 | 2-methyl-1,4-dihydronaphth...)
Affinity DataIC50: 7.10E+4nMAssay Description:Inhibition of UCHL3 in human H1299 cellsMore 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
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50552483(CHEMBL4763594)
Affinity DataIC50: 7.40E+4nMAssay Description:Inhibition of recombinant human UCHL3 assessed as reduction in cleavage of Ubiquitin-Rhodamine110-glycine to Ubiquitin and Rhodamine110-glycine using...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50538549(CHEMBL4641424)
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of human GST-tagged UCHL3 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
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50270667(CHEMBL4130194)
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of human GST-tagged UCHL3 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 sidPDB
In DepthDetails Article
PubMed
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM23421(1-benzyl-3-hydroxy-4-[(5-methylfuran-2-yl)carbonyl...)
Affinity DataIC50: 1.03E+5nMpH: 7.8 T: 2°CAssay Description:Enzyme reactions were carried out on Costar 96-well black assay plates. After the reaction, AMC fluorescence (excitation wavelength: 355 nm, emission...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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(Human)
Imperial College London

Curated by ChEMBL
LigandPNGBDBM50069762(CHEMBL3182437 | ML323 | US9802904, 87)
Affinity DataIC50: 1.14E+5nMpH: 7.5 T: 2°CAssay Description:Ubiquitin-7-amino-4-methylcoumarin (Ub-AMC) was generated as previously described.(7) The enzymatic reaction was conducted in fluorometric assay buff...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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