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Found 90 Enz. Inhib. hit(s) with Target = 'RAC-alpha serine/threonine-protein kinase [1-123]'
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
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
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
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
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
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
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
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 DataIC50:  6.30E+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
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 DataIC50:  1.00E+4nMAssay 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
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 DataIC50:  1.00E+4nMAssay 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
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 DataIC50:  1.50E+4nMAssay 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
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 DataIC50:  2.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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 DataIC50:  2.00E+4nMAssay 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
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223477(US9320734, 316)
Affinity DataIC50:  2.40E+4nMAssay 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
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223482(US9320734, 441)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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
LigandPNGBDBM50304367(CHEMBL595786 | N-(4-(N-(5-methyl-1,3,4-thiadiazol-...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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 DataIC50:  2.50E+4nMAssay 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
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 DataIC50: >5.00E+4nMAssay 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
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223483(US9320734, 445)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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
LigandPNGBDBM223473(US9320734, 444)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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
LigandPNGBDBM223475(US9320734, 345)
Affinity DataIC50:  5.00E+4nMAssay 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
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223485(US9320734, 456)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223481(US9320734, 439)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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 DataIC50: >5.00E+4nMAssay 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
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223484(US9320734, 450)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of AKT was measured by Western blotting using specific antibodies against phospho-Ser473-AKT in MiaPaCa-2 cells.Inhibition of AKT was meas...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
LigandPNGBDBM223477(US9320734, 316)
Affinity DataKd:  390nMAssay 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
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223475(US9320734, 345)
Affinity DataKd:  1.79E+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
LigandPNGBDBM223476(US9320734, 389)
Affinity DataKd:  4.58E+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
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetRAC-alpha serine/threonine-protein kinase [1-123](Homo sapiens (Human))
The University Of Texas System

US Patent
LigandPNGBDBM223474(US9320734, 415)
Affinity DataKd:  6.27E+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
Ligand InfoPC cidPC sid
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 DataKd:  1.51E+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 DataKd:  1.02E+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 DataKd:  1.02E+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 DataKd:  2.04E+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
LigandPNGBDBM50304369(4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonam...)
Affinity DataKd:  1.35E+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 DataKd:  450nMAssay 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 DataKd:  1.96E+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
LigandPNGBDBM50304369(4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonam...)
Affinity DataKd:  4.08E+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
LigandPNGBDBM50304369(4-dodecyl-N-(1,3,4-thiadiazol-2-yl)benzenesulfonam...)
Affinity DataKd:  1.35E+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
LigandPNGBDBM50338952(4-Dodecyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzen...)
Affinity DataKd:  8.32E+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
LigandPNGBDBM50338953(4-Dodecyl-N-(5-ethyl-1,3,4-thiadiazol-2-yl)benzene...)
Affinity DataKd:  7.59E+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
LigandPNGBDBM50338954(CHEMBL1685054 | N-(5-tert-Butyl-1,3,4-thiadiazol-2...)
Affinity DataKd:  4.07E+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
LigandPNGBDBM223478(US9320734, 110)
Affinity DataKd:  6.03E+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
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