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Found 148 with Last Name = 'gokhale' and Initial = 'v'
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM223480(US9320734, PtdIns(3,4,5)trisphosphate)
Affinity DataKi:  260nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304369(4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonam...)
Affinity DataKi:  2.40E+3nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304369(4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonam...)
Affinity DataKi:  2.40E+3nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338949(4-Tetradecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfo...)
Affinity DataKi:  6.70E+3nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338950(4-Hexadecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfon...)
Affinity DataKi:  6.90E+3nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338948(4-Octyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamid...)
Affinity DataKi:  8.40E+3nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338951(4-Octadecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfon...)
Affinity DataKi:  1.14E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304368(CHEMBL595582 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKi:  2.18E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338947(4-Hexyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamid...)
Affinity DataKi: >5.00E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304371(CHEMBL611216 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKi: >5.00E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50304370(CHEMBL593946 | N-(4-(N-1,3,4-thiadiazol-2-ylsulfam...)
Affinity DataKi: >5.00E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50034417(4-Amino-N-[1,3,4]thiadiazol-2-yl-benzenesulfonamid...)
Affinity DataKi: >5.00E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM50338946(4-Butyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonamid...)
Affinity DataKi: >5.00E+4nMAssay Description:SPR interaction analyses were performed with a Biacore 2000, using Biacore 2000 Control Software v3.2 and BIAevaluation v4.1 analysis software (Biaco...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308764(4-(3,4-Difluorophenyl)-N-(4-methyl-3-(3-methyl-4-o...)
Affinity DataIC50:  11nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308757(5-(4-Fluorophenyl)-N-(4-methyl-3-(3-methyl-4-oxo-3...)
Affinity DataIC50:  16nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM11639(4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...)
Affinity DataIC50:  30nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)
Affinity DataIC50:  38nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308758(5-(3-Chloro-4-fluorophenyl)-N-(4-methyl-3-(3-methy...)
Affinity DataIC50:  49nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308759(5-(4-Fluoro-3-methylphenyl)-N-(4-methyl-3-(3-methy...)
Affinity DataIC50:  60nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)
Affinity DataIC50:  84nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308761(CHEMBL591673 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  94nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308765(2-tert-Butyl-N-(4-methyl-3-(3-methyl-4-oxo-3,4-dih...)
Affinity DataIC50:  96nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308760(5-(3-Fluoro-4-methylphenyl)-N-(4-methyl-3-(3-methy...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308762(CHEMBL591526 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  105nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308766(CHEMBL605404 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  122nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308755(CHEMBL589415 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  405nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382181(CHEMBL1894768 | cid_684847)
Affinity DataIC50:  410nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308763(CHEMBL591661 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  468nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382182(CHEMBL2023858)
Affinity DataIC50:  810nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382192(CHEMBL2023847)
Affinity DataIC50:  840nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382180(CHEMBL2023859)
Affinity DataIC50:  910nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382177(CHEMBL2023862)
Affinity DataIC50:  910nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382178(CHEMBL2023861)
Affinity DataIC50:  920nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382179(CHEMBL2023860)
Affinity DataIC50:  930nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM223474(US9320734, 415)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of AKT was measured by Western blots using specific antibodies against phospho-Ser473-AKT in HT-29 lung cancer cells. Inhibition of the ph...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382190(CHEMBL2023850)
Affinity DataIC50:  1.08E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382184(CHEMBL2023857)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382183(CHEMBL1622194)
Affinity DataIC50:  1.37E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382191(CHEMBL2023848)
Affinity DataIC50:  1.39E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50308756(CHEMBL605198 | N-(4-Methyl-3-(3-methyl-4-oxo-3,4-d...)
Affinity DataIC50:  1.65E+3nMAssay Description:Inhibition of human recombinant full length p38alpha assessed as MAPKAPK2 phosphorylation by [32P]ATP SDS-PAGE gel kinase assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University of Texas System

US Patent
LigandPNGBDBM223476(US9320734, 389)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of AKT was measured by Western blots using specific antibodies against phospho-Ser473-AKT in HT-29 lung cancer cells. Inhibition of the ph...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382195(CHEMBL2023950)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382194(CHEMBL1903990)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382189(CHEMBL2023851)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382188(CHEMBL2023852)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382187(CHEMBL2023853)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382186(CHEMBL1907465)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382185(CHEMBL1907447)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382176(CHEMBL1902481 | cid_867556)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
The University Of Arizona

Curated by ChEMBL
LigandPNGBDBM50382175(CHEMBL2023948)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of COX2 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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