Compile Data Set for Download or QSAR
Report error Found 41 Enz. Inhib. hit(s) with all data for entry = 50013369
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataEC50:  1.70E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as reduction in TNFalpha-induced necroptosis measured after 24 hrs by MTS ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataEC50:  1.70E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565167(CHEMBL4799016)
Affinity DataEC50:  1.44E+4nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565168(CHEMBL4778912)
Affinity DataEC50: >2.50E+4nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565169(CHEMBL4797106)
Affinity DataEC50:  2.20E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565170(CHEMBL4784995)
Affinity DataEC50:  1.04E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565171(CHEMBL4785154)
Affinity DataEC50:  2.50E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565172(CHEMBL4787708)
Affinity DataEC50:  1.81E+4nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565173(CHEMBL4780623)
Affinity DataEC50:  9.00E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565174(CHEMBL4782744)
Affinity DataEC50:  4.40E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565175(CHEMBL4786704)
Affinity DataEC50:  8.90E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565176(CHEMBL4790129)
Affinity DataEC50:  6.90E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataEC50:  4.70E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50519641(CHEMBL4439426)
Affinity DataEC50:  1.10E+3nMAssay Description:Inhibition of RIPK1 in human FADD-deficient Jurkat I 2.1 cells assessed as protection against TNFalpha-induced necroptosis measured after 24 hrs by M...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 480nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in baculovirus infected Sf9 insect cells using YSPTSPSYSPTSPSYSPTSPSKKKK as substrate by ADP-...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCasein kinase I isoform delta(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565165(CHEMBL4780812)
Affinity DataIC50: 680nMAssay Description:Inhibition of CK1delta (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetDual specificity protein kinase CLK1(Mouse)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 800nMAssay Description:Inhibition of mouse recombinant CLK1 expressed in bacterial expression system using GRSRSRSRSRSR as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Rat)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of recombinant rat DYRK1A kinase domain (1 to 499 residues) expressed in bacterial expression system using KKISGRLSPIMTEQ as substrate by ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Rat)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 2.21E+3nMAssay Description:Inhibition of recombinant rat DYRK1A kinase domain (1 to 499 residues) expressed in bacterial expression system using KKISGRLSPIMTEQ as substrate by ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 2.89E+3nMAssay Description:Inhibition of recombinant human RIPK1 kinase domain (8 to 322 residues) using myelin basic protein as substrate measured after 120 mins by [gamma-32P...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetAurora kinase B(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human AURKB expressed in baculovirus infected Sf9 insect cells using myelin basic protein as substrate by ADP-Glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 3(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human RIPK3 expressed in baculovirus infected Sf9 insect cells using myelin basic protein as substrate by ADP-Glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 3(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human RIPK3 expressed in baculovirus infected Sf9 insect cells using myelin basic protein as substrate by ADP-Glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetTyrosine-protein kinase ABL1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human ABL1 (118 to 535 residues) expressed in baculovirus infected Sf9 insect cells using EAIYAAPFAKKK as substrate by ADP-...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetAurora kinase B(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human AURKB expressed in baculovirus infected Sf9 insect cells using myelin basic protein as substrate by ADP-Glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetTyrosine-protein kinase ABL1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human ABL1 (118 to 535 residues) expressed in baculovirus infected Sf9 insect cells using EAIYAAPFAKKK as substrate by ADP-...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetTyrosine-protein kinase JAK3(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human JAK3 C-terminal domain (781 to 1124 residues) expressed in baculovirus infected Sf9 insect cells using GGEEEEYFELVKKK...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetTyrosine-protein kinase JAK3(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human JAK3 C-terminal domain (781 to 1124 residues) expressed in baculovirus infected Sf9 insect cells using GGEEEEYFELVKKK...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCasein kinase I isoform epsilon(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human CK1epsilon expressed in baculovirus infected Sf9 insect cells using RRKHAAIGSpAYSITA as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCasein kinase I isoform epsilon(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human CK1epsilon expressed in baculovirus infected Sf9 insect cells using RRKHAAIGSpAYSITA as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetSerine/threonine-protein kinase pim-1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human PIM1 expressed in bacterial expression system using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetSerine/threonine-protein kinase pim-1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human PIM1 expressed in bacterial expression system using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetSerine/threonine-protein kinase haspin(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human HASPIN kinase domain (470 to 798 residues) expressed in bacterial expression system using histone H3(1-21) peptide as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetSerine/threonine-protein kinase haspin(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of recombinant human HASPIN kinase domain (470 to 798 residues) expressed in bacterial expression system using histone H3(1-21) peptide as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetDual specificity protein kinase CLK1(Mouse)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of mouse recombinant CLK1 expressed in bacterial expression system using GRSRSRSRSRSR as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CDK9/cyclin T expressed in baculovirus infected Sf9 insect cells using YSPTSPSYSPTSPSYSPTSPSKKKK as substrate by ADP-...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-dependent kinase 5 activator 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CDK5/p25 expressed in bacterial expression using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-dependent kinase 5 activator 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant CDK5/p25 expressed in bacterial expression using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565177(CHEMBL4796622)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human CDK2/cyclin A using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human CDK2/cyclin A using histone H1 as substrate by ADP-glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50565166(CHEMBL4776698)
Affinity DataIC50: 1.21E+4nMAssay Description:Inhibition of recombinant human RIPK1 kinase domain (8 to 322 residues) using myelin basic protein as substrate measured after 120 mins by [gamma-32P...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed