Report error Found 130 with Last Name = 'kojima' and Initial = 's'
Affinity DataIC50: 380nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 520nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 700nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 900nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Human)
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
Affinity DataIC50: 910nMAssay Description:Inhibition of human recombinant MBP-KAT2 expressed in HEK293 cells assessed as conversion of L-kynurenine to kynurenic acid after 1 hrMore data for this Ligand-Target Pair
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Rat)
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of rat brain KAT2More data for this Ligand-Target Pair
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Human)
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of KAT2 in human prefrontal cortex homogenatesMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Human)
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
University of Piemonte Orientale Amedeo Avogadro
Curated by ChEMBL
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human recombinant MBP-KAT2 expressed in HEK293 cells assessed as conversion of L-kynurenine to kynurenic acid after 1 hrMore data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of Vaccinia H1-related phosphatase (unknown origin) by fluorescence emission assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 2.00E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 2.40E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 3.60E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory activity against vaccinia VH1-related phosphatase(VHR)More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibitory activity against vaccinia VH1-related phosphatase(VHR)More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of Vaccinia H1-related phosphatase (unknown origin) by fluorescence emission assay in presence of 0.001% NP-40More data for this Ligand-Target Pair
Affinity DataIC50: 4.60E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibitory activity against vaccinia VH1-related phosphatase(VHR)More data for this Ligand-Target Pair
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 6.70E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of hypoxia-induced HIF1 alpha transcriptional activity in human HeLa cells transfected with luciferase reporter containing of HRE assessed...More data for this Ligand-Target Pair
Affinity DataIC50: 7.30E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 7.70E+3nMAssay Description:Inhibition of Vaccinia H1-related phosphatase (unknown origin) by fluorescence emission assay in presence of 0.001% NP-40More data for this Ligand-Target Pair
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibitory activity against cell division cycle 25BMore data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+3nMAssay Description:The biological activity of a compound was determined by measuring the activation of Smad3/Smad4 complex which is a transcription factor showing activ...More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of Vaccinia H1-related phosphatase (unknown origin) by fluorescence emission assay in presence of 0.001% NP-40More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 9.20E+3nMAssay Description:Inhibitory activity against vaccinia VH1-related phosphatase(VHR)More data for this Ligand-Target Pair
TargetDual specificity protein phosphatase 3(Human)
Japan Science and Technology Agency
Curated by ChEMBL
Japan Science and Technology Agency
Curated by ChEMBL
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibitory activity against vaccinia VH1-related phosphatase(VHR)More data for this Ligand-Target Pair