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Found 71 with Last Name = 'nicholson' and Initial = 'b'
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436151(CHEMBL2398212)
Affinity DataIC50:  420nMAssay Description:Inhibition of USP7 (unknown origin) using ubiquitin-EKL as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436152(SPONGIACIDIN C)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of USP7 (unknown origin) using ubiquitin-EKL as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 21(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436152(SPONGIACIDIN C)
Affinity DataIC50:  1.66E+4nMAssay Description:Inhibition of core catalytic domain of USP21 (unknown origin) using ubiquitin-Rh110 as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436149(CHEMBL2398214)
Affinity DataIC50:  2.26E+4nMAssay Description:Inhibition of USP7 (unknown origin) using ubiquitin-EKL as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436150(CHEMBL2398213)
Affinity DataIC50:  2.81E+4nMAssay Description:Inhibition of USP7 (unknown origin) using ubiquitin-EKL as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 2(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436152(SPONGIACIDIN C)
Affinity DataIC50: >3.16E+4nMAssay Description:Inhibition of core catalytic domain of USP2 (unknown origin) using diubiquitin IQF K4804 as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 8(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436152(SPONGIACIDIN C)
Affinity DataIC50: >3.16E+4nMAssay Description:Inhibition of core catalytic domain of USP8 (unknown origin) using ubiquitin-Rh110 as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSentrin-specific protease 1(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50436152(SPONGIACIDIN C)
Affinity DataIC50: >3.16E+4nMAssay Description:Inhibition of core catalytic domain of SENP1 (unknown origin) using SUMO3-EKL as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393437(CHEMBL2159495)
Affinity DataEC50:  4.20E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393438(CHEMBL2159496)
Affinity DataEC50: >3.16E+4nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393439(CHEMBL2159497)
Affinity DataEC50:  6.90E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393440(CHEMBL2159498)
Affinity DataEC50:  8.00E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393441(CHEMBL2159499)
Affinity DataEC50:  2.20E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393442(CHEMBL2159501)
Affinity DataEC50:  1.70E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393443(CHEMBL2159502)
Affinity DataEC50:  7.80E+3nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393444(CHEMBL2159503)
Affinity DataEC50:  380nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393445(CHEMBL2159504)
Affinity DataEC50:  430nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393446(CHEMBL2159505)
Affinity DataEC50:  400nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393438(CHEMBL2159496)
Affinity DataEC50:  1.40E+4nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393439(CHEMBL2159497)
Affinity DataEC50:  3.70E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393440(CHEMBL2159498)
Affinity DataEC50:  8.70E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393441(CHEMBL2159499)
Affinity DataEC50:  2.20E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393450(CHEMBL2159500)
Affinity DataEC50:  1.20E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393442(CHEMBL2159501)
Affinity DataEC50:  1.30E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393443(CHEMBL2159502)
Affinity DataEC50:  5.50E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393444(CHEMBL2159503)
Affinity DataEC50:  530nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393445(CHEMBL2159504)
Affinity DataEC50:  870nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393446(CHEMBL2159505)
Affinity DataEC50:  500nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393447(CHEMBL2159506)
Affinity DataEC50: >3.16E+4nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393448(CHEMBL2159507)
Affinity DataEC50:  350nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393449(CHEMBL2159508)
Affinity DataEC50:  1.00E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393447(CHEMBL2159506)
Affinity DataEC50:  1.90E+4nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393448(CHEMBL2159507)
Affinity DataEC50:  380nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 7(Homo sapiens (Human))
Kumamoto University

Curated by ChEMBL
LigandPNGBDBM50393449(CHEMBL2159508)
Affinity DataEC50:  420nMAssay Description:Inhibition of recombinant USP7 expressed in Sf9 cells by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUbiquitin carboxyl-terminal hydrolase 47(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50393437(CHEMBL2159495)
Affinity DataEC50:  4.30E+3nMAssay Description:Inhibition of USP47 by Ub-CHOP reporter assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTubulin beta chain(Sus scrofa)
Tokyo University Of Pharmacy And Life Sciences

Curated by ChEMBL
LigandPNGBDBM50030765(NPI-2358 | Plinabulin)
Affinity DataKd:  1.06E+3nMAssay Description:Binding affinity to porcine tubulin after 1 hr by spectrofluorometric analysisMore data for this Ligand-Target Pair
TargetTubulin beta chain(Sus scrofa)
Tokyo University Of Pharmacy And Life Sciences

Curated by ChEMBL
LigandPNGBDBM50485035(CHEMBL2024561)
Affinity DataKd:  620nMAssay Description:Binding affinity to porcine tubulin after 1 hr by spectrofluorometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTubulin beta chain(Sus scrofa)
Tokyo University Of Pharmacy And Life Sciences

Curated by ChEMBL
LigandPNGBDBM50485036(CHEMBL2024544)
Affinity DataKd:  200nMAssay Description:Binding affinity to porcine tubulin after 1 hr by spectrofluorometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566321(CHEMBL4867267)
Affinity DataEC50:  1.20nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566322(CHEMBL4853705)
Affinity DataEC50:  1.20nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566323(CHEMBL4860414)
Affinity DataEC50:  0.900nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566324(CHEMBL4851358)
Affinity DataEC50:  1.30nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566325(CHEMBL4846860)
Affinity DataEC50:  1.20nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566326(CHEMBL4860893)
Affinity DataEC50:  2.30nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566327(CHEMBL4868831)
Affinity DataEC50:  4.70nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566328(CHEMBL4869259)
Affinity DataEC50:  4nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566329(CHEMBL4868773)
Affinity DataEC50:  38nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566330(CHEMBL4874774)
Affinity DataEC50: <0.5nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566331(CHEMBL4874354)
Affinity DataEC50:  2.5nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtein arginine N-methyltransferase 5(Homo sapiens (Human))
Merck

Curated by ChEMBL
LigandPNGBDBM50566332(CHEMBL4848739)
Affinity DataEC50:  14nMAssay Description:Inhibition of PRMT5 (unknown origin) assessed as inhibition of symmetric dimethylation of arginine incubated for 3 days by fluorescence based cellula...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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