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Found 73 with Last Name = 'hanna' and Initial = 'c'
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026212(CHEMBL1276185)
Affinity DataIC50: <0.100nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026207(CHEMBL1276170)
Affinity DataIC50: <0.100nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330925(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  0.110nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330905(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  0.160nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330924(7-(2-fluoro-4-((1S,4S)-5-methyl-2,5-diazabicyclo[2...)
Affinity DataIC50:  0.230nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026206(CHEMBL1276195)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026208(CHEMBL1276193)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026210(CHEMBL1276196)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026211(CHEMBL1276184)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026209(CHEMBL1276171)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50026205(CHEMBL1276194)
Affinity DataIC50: <0.320nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330923(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)-7-(2,3,5,6-te...)
Affinity DataIC50:  0.350nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50311985(3-(7-(4-((1S,4S)-5-methyl-2,5-diazabicyclo[2.2.1]h...)
Affinity DataIC50:  0.380nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330922(7-(2,5-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  0.380nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330921((1S,4S)-2-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)...)
Affinity DataIC50:  0.410nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330920(3-(7-fluoro-1H-indazol-4-yl)-7-(4-((1S,4S)-5-methy...)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330919(3-(1H-indazol-4-yl)-7-(2-methyl-4-((1S,4S)-5-methy...)
Affinity DataIC50:  0.510nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330918((1R,4R)-5-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)...)
Affinity DataIC50:  0.520nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330917(7-(2,3-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  0.610nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330916((1S,4S)-2-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)...)
Affinity DataIC50:  0.710nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330915(9-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)pyrazolo...)
Affinity DataIC50:  0.770nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330914(3-(1H-indazol-4-yl)-7-(4-((1S,4S)-5-methyl-2,5-dia...)
Affinity DataIC50:  1nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330912((1S,4S)-5-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)...)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330913(3-(1H-indazol-4-yl)-7-(4-((1S,4S)-5-methyl-2,5-dia...)
Affinity DataIC50:  1.20nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330911(3-(1H-indazol-4-yl)-7-(4-((1S,4S)-5-methyl-2,5-dia...)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330910(7-(4-fluoro-2-((1R,4R)-2-methyl-2-azabicyclo[2.2.1...)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330909(7-(3-fluoro-4-((1S,4S)-5-methyl-2,5-diazabicyclo[2...)
Affinity DataIC50:  1.90nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330908(3-(1H-indazol-4-yl)-7-(4-((1S,4S)-5-methyl-2,5-dia...)
Affinity DataIC50:  2nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330907(7-(4-((1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-ylme...)
Affinity DataIC50:  2.30nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsoleucine--tRNA ligase(Staphylococcus aureus)
Smithkline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50470911(CHEMBL122825)
Affinity DataIC50:  4.45nMAssay Description:Inhibitory activity against isoleucyl-tRNA synthetase (IRS) of Staphylococcus aureusMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetIsoleucine--tRNA ligase(Staphylococcus aureus)
Smithkline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50470914(CHEMBL120343)
Affinity DataIC50:  6.67nMAssay Description:Inhibitory activity against isoleucyl-tRNA synthetase (IRS) of Staphylococcus aureus NCTC 3571More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetIsoleucine--tRNA ligase(Staphylococcus aureus)
Smithkline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50470913(CHEMBL120798)
Affinity DataIC50:  6.87nMAssay Description:Inhibitory activity against isoleucyl-tRNA synthetase (IRS) of Staphylococcus aureusMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330906(2-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)pyrazolo[1,...)
Affinity DataIC50:  7.30nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsoleucine--tRNA ligase(Staphylococcus aureus)
Smithkline Beecham Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50470912(CHEMBL120437)
Affinity DataIC50:  7.98nMAssay Description:Inhibitory activity against isoleucyl-tRNA synthetase (IRS) of Staphylococcus aureusMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330905(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  8.5nMAssay Description:Inhibition of C-rafMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330904(7-(3,5-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  9.60nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330903((1S,4S)-5-(4-(3-(1H-indazol-4-yl)-2-(pyridin-4-yl)...)
Affinity DataIC50:  10nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29511(Pyranonaphthoquinone (PNQ) lactone, 11a)
Affinity DataIC50:  44nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29512(Pyranonaphthoquinone (PNQ) lactone, 11b)
Affinity DataIC50:  57nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase B-raf(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330902(3-(1H-indazol-4-yl)-7-(3-((1S,4S)-5-methyl-2,5-dia...)
Affinity DataIC50:  61nMAssay Description:Inhibition of BRAFMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29513(Pyranonaphthoquinone (PNQ) lactone, 11c)
Affinity DataIC50:  72nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29514(Pyranonaphthoquinone (PNQ) lactone, 11d)
Affinity DataIC50:  80nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEphrin type-A receptor 1(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330905(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  95nMAssay Description:Inhibition of EPHA1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29515(Pyranonaphthoquinone (PNQ) lactone, 11e)
Affinity DataIC50:  99nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29516(Pyranonaphthoquinone (PNQ) lactone, 11f)
Affinity DataIC50:  122nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330905(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  145nMAssay Description:Inhibition of MAPK14More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29506(Lactoquinomycin | Lactoquinomycin A)
Affinity DataIC50:  149nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29517(Pyranonaphthoquinone (PNQ) lactone, 11g)
Affinity DataIC50:  150nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50330905(7-(2,6-difluoro-4-((1S,4S)-5-methyl-2,5-diazabicyc...)
Affinity DataIC50:  160nMAssay Description:Inhibition of RETMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase(Homo sapiens (Human))
Wyeth Research

LigandPNGBDBM29518(Pyranonaphthoquinone (PNQ) lactone, 11h)
Affinity DataIC50:  163nMpH: 7.4 T: 2°CAssay Description:AKT1 was assayed using constitutively active Myr-AKT1 in low-binding 96-well plates. The kinase reactions were initiated by the addition of assay mix...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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