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Report error Found 29 Enz. Inhib. hit(s) with all data for entry = 1889
TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14805(3-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  1.40E+3nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

LigandPNGBDBM14805(3-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  1.50E+3nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14803(2-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  2.30E+3nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB
PDB3D3D Structure (crystal)

LigandPNGBDBM14804(1-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  3.70E+3nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14803(2-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  5.00E+3nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14804(1-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50:  5.50E+3nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14801(2-({5,6-diphenylfuro[2,3-d]pyrimidin-4-yl}(methyl)...)
Affinity DataIC50:  6.10E+3nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB
PDB3D3D Structure (crystal)

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14799(2-[5,6-Bis-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin...)
Affinity DataIC50:  1.54E+4nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB
PDB3D3D Structure (crystal)

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14800(2-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-et...)
Affinity DataIC50:  2.09E+4nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14802((5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-acet...)
Affinity DataIC50:  2.29E+4nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedMMDB
PDB3D3D Structure (crystal)

LigandPNGBDBM14799(2-[5,6-Bis-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin...)
Affinity DataIC50:  2.94E+4nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14810(2-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-2-...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14809(N-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-yl)-benzami...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14812((5,6-Diphenyl-furo[2,3-d]pyrimidin-4-yl)-(2-methox...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14813(2-({5,6-diphenylfuro[2,3-d]pyrimidin-4-yl}amino)pr...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14811(N-(2-aminoethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14806(5,6-Diphenyl-furo[2,3-d]pyrimidin-4 -ylamine | 5,6...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14807(3-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-pr...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetSerine/threonine-protein kinase Chk1(Human)
Vernalis (R&D)

LigandPNGBDBM14808(Benzyl-(5,6-diphenyl-furo[2,3-d]pyrimidin-4-yl)-am...)
Affinity DataIC50: >1.00E+5nMpH: 7.5 T: 30°CAssay Description:Chk1 kinase activity was assayed in reaction buffer containing substrate peptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P] ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14801(2-({5,6-diphenylfuro[2,3-d]pyrimidin-4-yl}(methyl)...)
Affinity DataIC50:  1.11E+5nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14802((5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-acet...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14800(2-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-et...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human CDK1 kinase activity was assayed in reaction buffer containing substrate Histone H1, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14799(2-[5,6-Bis-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14800(2-(5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-et...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14801(2-({5,6-diphenylfuro[2,3-d]pyrimidin-4-yl}(methyl)...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14805(3-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14802((5,6-Diphenyl-furo[2,3-d]pyrimidin-4-ylamino)-acet...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14803(2-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

LigandPNGBDBM14804(1-(5,6-Diphenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylami...)
Affinity DataIC50: >2.00E+5nMpH: 7.5 T: 30°CAssay Description:Human PKA kinase activity was assayed in reaction buffer containing substrate Kemptide, enzyme, and inhibitor in the presence of 100uM ATP/[gamma-33P...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed