Compile Data Set for Download or QSAR
Found 74 with Last Name = 'herrmann' and Initial = 'l'
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395894(CHEMBL2163771)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395890(CHEMBL2163774)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395894(CHEMBL2163771)copy SMILEScopy InChI
Affinity DataKi:  70nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395887(CHEMBL2163770)copy SMILEScopy InChI
Affinity DataKi:  90nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  110nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  600nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395894(CHEMBL2163771)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395888(CHEMBL2163769)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395887(CHEMBL2163770)copy SMILEScopy InChI
Affinity DataKi:  1.60E+3nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395887(CHEMBL2163770)copy SMILEScopy InChI
Affinity DataKi:  2.10E+3nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395893(CHEMBL1165662)copy SMILEScopy InChI
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM7453(1-aza-9-oxafluorene deriv. 7b | 4-methoxy-3-phenyl...)copy SMILEScopy InChI
Affinity DataKi:  5.30E+3nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395893(CHEMBL1165662)copy SMILEScopy InChI
Affinity DataKi:  5.80E+3nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395888(CHEMBL2163769)copy SMILEScopy InChI
Affinity DataKi:  5.80E+3nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395893(CHEMBL1165662)copy SMILEScopy InChI
Affinity DataKi:  6.40E+3nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM7453(1-aza-9-oxafluorene deriv. 7b | 4-methoxy-3-phenyl...)copy SMILEScopy InChI
Affinity DataKi:  1.48E+4nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM7453(1-aza-9-oxafluorene deriv. 7b | 4-methoxy-3-phenyl...)copy SMILEScopy InChI
Affinity DataKi:  2.40E+4nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395888(CHEMBL2163769)copy SMILEScopy InChI
Affinity DataKi:  2.53E+4nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395890(CHEMBL2163774)copy SMILEScopy InChI
Affinity DataKi:  2.61E+4nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395891(CHEMBL2163773)copy SMILEScopy InChI
Affinity DataKi:  1.47E+5nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM7453(1-aza-9-oxafluorene deriv. 7b | 4-methoxy-3-phenyl...)copy SMILEScopy InChI
Affinity DataKi:  2.17E+5nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  2.96E+5nMAssay Description:Inhibition of EGFRMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 6/G1/S-specific cyclin-D1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi:  7.73E+5nMAssay Description:Inhibition of CDK6/Cyclin D1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetProtein kinase C gamma type(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of PKCgammaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetProtein kinase C epsilon type(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of PKCepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetProtein kinase C iota type(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of PKCiotaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of ERBB2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of TIE2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of WEE1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCasein kinase I isoform alpha(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of Ck1alpha1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395891(CHEMBL2163773)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395889(CHEMBL2163768)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of GSK3betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395890(CHEMBL2163774)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395891(CHEMBL2163773)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395889(CHEMBL2163768)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1/G1/S-specific cyclin-E2(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395889(CHEMBL2163768)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK2/Cyclin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395893(CHEMBL1165662)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395889(CHEMBL2163768)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK5/p25More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
Martin-Luther University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50395892(CHEMBL2163772)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of PKCalphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395891(CHEMBL2163773)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
LigandPNGBDBM50395890(CHEMBL2163774)copy SMILEScopy InChI
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of CDK1/Cyclin BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M61MC1PubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM50009854(CHEMBL13078 | [1-(2-Morpholin-4-yl-ethyl)-1H-indol...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM50009864(CHEMBL274833 | [2-Methyl-1-(2-morpholin-4-yl-ethyl...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM50009871(Benzo[b]thiophen-3-yl-[2-methyl-1-(2-morpholin-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM50406486(CHEMBL2092862)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM50009856(CHEMBL13376 | Clometacin | [3-(4-Chloro-benzoyl)-6...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
TargetProstaglandin-H2 D-isomerase(Mus musculus)
Sterling Research Group

Curated by ChEMBL
LigandPNGBDBM85511(CAS_74103-07-4 | KETOROLAC | Ketorolac tris salt |...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Concentration required to inhibit 50% activity of prostaglandin synthetase was determined in vitro in mouse brain microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24M955SPubMed
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