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Found 28 with Last Name = 'wallace' and Initial = 'mj'
TargetProtein kinase C epsilon type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human PKCepsilonMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C epsilon type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM2683(2-[1-(3-dimethylaminopropyl)-indol-3-yl]-3-(indol-...)
Affinity DataIC50:  6nMAssay Description:Inhibition of human PKCepsilonMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C gamma type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)
Affinity DataIC50:  18nMAssay Description:Inhibition of human PKCgammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C gamma type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM2683(2-[1-(3-dimethylaminopropyl)-indol-3-yl]-3-(indol-...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human PKCgammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM2683(2-[1-(3-dimethylaminopropyl)-indol-3-yl]-3-(indol-...)
Affinity DataIC50:  32nMAssay Description:Inhibition of human PKCdeltaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)
Affinity DataIC50:  41nMAssay Description:Inhibition of human PKCdeltaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C iota type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)
Affinity DataIC50:  364nMAssay Description:Inhibition of human PKCiotaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190582(CHEMBL3827911)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190581(CHEMBL3828161)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190578(CHEMBL3827297)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C iota type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM2683(2-[1-(3-dimethylaminopropyl)-indol-3-yl]-3-(indol-...)
Affinity DataIC50:  3.46E+3nMAssay Description:Inhibition of human PKCiotaMore data for this Ligand-Target Pair
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190579(CHEMBL3828532)
Affinity DataIC50:  8.10E+3nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190580(CHEMBL3828019)
Affinity DataIC50:  9.40E+3nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190584(CHEMBL3828105)
Affinity DataIC50:  1.13E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190583(CHEMBL3827459)
Affinity DataIC50:  1.15E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190583(CHEMBL3827459)
Affinity DataIC50:  1.52E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190585(CHEMBL3828540)
Affinity DataIC50:  1.71E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr in presence of sodium pyrophospha...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190584(CHEMBL3828105)
Affinity DataIC50:  1.78E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190585(CHEMBL3828540)
Affinity DataIC50:  1.86E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190580(CHEMBL3828019)
Affinity DataIC50:  1.93E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190578(CHEMBL3827297)
Affinity DataIC50:  2.06E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190579(CHEMBL3828532)
Affinity DataIC50:  2.25E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190582(CHEMBL3827911)
Affinity DataIC50:  2.68E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDihydropteroate synthase(Bacillus anthracis)
St. Jude Children'S Research Hospital

Curated by ChEMBL
LigandPNGBDBM50190581(CHEMBL3828161)
Affinity DataIC50: >6.25E+4nMAssay Description:Inhibition of fluorescein-labeled probe binding to Bacillus anthracis N-terminal His-tagged DHPS incubated for 1 hr by fluorescence polarization assa...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C iota type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50229961(1-(1,1-dimethylethyl)-3-(1-naphthalenyl)-1H-pyrazo...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PKCiotaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C gamma type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50229961(1-(1,1-dimethylethyl)-3-(1-naphthalenyl)-1H-pyrazo...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PKCgammaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50229961(1-(1,1-dimethylethyl)-3-(1-naphthalenyl)-1H-pyrazo...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PKCdeltaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C epsilon type(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50229961(1-(1,1-dimethylethyl)-3-(1-naphthalenyl)-1H-pyrazo...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PKCepsilonMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed