Found 101 with Last Name = 'zhao' and Initial = 'jy' 
Affinity DataIC50: 170nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 210nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 340nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 360nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 380nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 410nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 420nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 420nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 510nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 570nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 580nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 590nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.01E+3nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 1.39E+3nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 1.66E+3nMAssay Description:Inhibition of human PHGDH expressed in Escherichia coli BL21 using 3-PG as substrate incubated for 30 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Shanghai University Of Traditional Chinese Medicine
Curated by ChEMBL
Shanghai University Of Traditional Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 5.18E+3nMAssay Description:Displacement of 5-FAM-GpYLPQTV-NH2 from His-tagged STAT3 (unknown origin) (127 to 722 residues) incubated for 30 mins followed by fluorescent peptide...More data for this Ligand-Target Pair
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Shanghai University Of Traditional Chinese Medicine
Curated by ChEMBL
Shanghai University Of Traditional Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 5.55E+3nMAssay Description:Displacement of 5-FAM-GpYLPQTV-NH2 from His-tagged STAT3 (unknown origin) (127 to 722 residues) incubated for 30 mins followed by fluorescent peptide...More data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences
Curated by ChEMBL
Chinese Academy Of Sciences
Curated by ChEMBL
Affinity DataIC50: 6.43E+3nMAssay Description:Inhibition of PTP-1B (unknown origin) using pNPP substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences
Curated by ChEMBL
Chinese Academy Of Sciences
Curated by ChEMBL
Affinity DataIC50: 6.54E+3nMAssay Description:Inhibition of PTP-1B (unknown origin) using pNPP substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences
Curated by ChEMBL
Chinese Academy Of Sciences
Curated by ChEMBL
Affinity DataIC50: 7.12E+3nMAssay Description:Inhibition of PTP-1B (unknown origin) using pNPP substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences
Curated by ChEMBL
Chinese Academy Of Sciences
Curated by ChEMBL
Affinity DataIC50: 7.32E+3nMAssay Description:Inhibition of PTP-1B (unknown origin) using pNPP substrate measured after 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: 9.76E+3nMAssay Description:Inhibition of human PHGDH expressed in Escherichia coli BL21 using 3-PG as substrate incubated for 30 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 1.04E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate by fluorescence based analysisMore data for this Ligand-Target Pair
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences
Curated by ChEMBL
Chinese Academy Of Sciences
Curated by ChEMBL
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of PTP-1B (unknown origin) using pNPP substrate measured after 30 minsMore data for this Ligand-Target Pair
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Xinjiang Technical Institute Of Physics And Chemistry
Curated by ChEMBL
Xinjiang Technical Institute Of Physics And Chemistry
Curated by ChEMBL
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of PARP1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 2.16E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: 2.25E+4nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 2.81E+4nMAssay Description:Inhibition of human full-length PHGDH incubated for 10 mins by SPR analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.48E+4nMAssay Description:Inhibition of human full-length PHGDH incubated for 10 mins by SPR analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.57E+4nMAssay Description:Inhibition of human full-length PHGDH incubated for 10 mins by SPR analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.64E+4nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 4.20E+4nMAssay Description:Inhibition of human full-length PHGDH incubated for 10 mins by SPR analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 4.59E+4nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: <5.00E+4nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 5.70E+4nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
3D Structure (crystal)
Affinity DataIC50: 6.73E+4nMAssay Description:Inhibition of human PHGDH by fluorescence based analysisMore data for this Ligand-Target Pair
Ligand Info
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human PHGDH using 3-PG as substrate incubated for 60 mins by fluorescence based analysisMore data for this Ligand-Target Pair
