Compile Data Set for Download or QSAR
Found 86 with Last Name = 'ye' and Initial = 'xs'
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501643(CHEMBL4065191)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127702(CHEMBL3629697)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501640(CHEMBL4102509)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501638(CHEMBL4091389)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127703(CHEMBL3629696)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)copy SMILEScopy InChI
Affinity DataKi:  29nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501642(CHEMBL3629698)copy SMILEScopy InChI
Affinity DataKi:  29nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501637(CHEMBL4063545)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)copy SMILEScopy InChI
Affinity DataKi:  106nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501644(CHEMBL4097206)copy SMILEScopy InChI
Affinity DataKi:  106nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501641(CHEMBL4081024)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50501639(CHEMBL4083608)copy SMILEScopy InChI
Affinity DataKi:  224nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)copy SMILEScopy InChI
Affinity DataKi:  436nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127706(CHEMBL3629692)copy SMILEScopy InChI
Affinity DataKi:  436nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127704(CHEMBL3629694)copy SMILEScopy InChI
Affinity DataKi:  865nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127705(CHEMBL3629693)copy SMILEScopy InChI
Affinity DataKi:  1.51E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127707(CHEMBL3629691)copy SMILEScopy InChI
Affinity DataKi:  4.31E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)copy SMILEScopy InChI
Affinity DataKi:  5.85E+3nMAssay Description:Competitive inhibition of human recombinant ST6Gal-1 using CMP-Neu5Ac and p-nitrophenyl LacNAc as donar and acceptor by Lineweaver-Burk double recipr...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20V8FMQPubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50127709(CHEMBL3629689)copy SMILEScopy InChI
Affinity DataKi:  5.85E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged ST6Gal-1 (44 to 406 residues) using CMP-Neu5Ac as substrate after 20 mins by UV/RP-HPLC methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2XP77Z0PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279531((7Beta-Hydroxy)-Morroniside | CHEBI:80852 | Morron...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279545((7Alpha-Hydroxy)-Morroniside | CHEMBL2152455)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279554(CHEMBL4174708)copy SMILEScopy InChI
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279550(CHEMBL4159173)copy SMILEScopy InChI
Affinity DataIC50: 1.22E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279529(CHEBI:15771 | Loganin)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279530(CHEMBL4175770)copy SMILEScopy InChI
Affinity DataIC50: 1.94E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279552(CHEMBL4164481)copy SMILEScopy InChI
Affinity DataIC50: 2.19E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279567(7-Epi-Loganin | 8-Epiloganin | CHEMBL1081586)copy SMILEScopy InChI
Affinity DataIC50: 2.29E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279546(CHEMBL1209872)copy SMILEScopy InChI
Affinity DataIC50: 2.48E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM19459(5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataIC50: 2.48E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279542(CHEMBL4167909)copy SMILEScopy InChI
Affinity DataIC50: 2.76E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279553(CHEMBL4160655)copy SMILEScopy InChI
Affinity DataIC50: 2.97E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279547(CHEMBL2152454)copy SMILEScopy InChI
Affinity DataIC50: 3.25E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279533(CHEMBL4163373)copy SMILEScopy InChI
Affinity DataIC50: 4.05E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279551(CHEMBL4172359)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50413911(CHEMBL449940)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of human placental beta-glucocerebrosidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W9CBWPubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279569(CHEMBL4171260)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279549(CHEMBL4174085)copy SMILEScopy InChI
Affinity DataIC50: 5.26E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279556(CHEMBL4167273)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279548(CHEMBL4166828)copy SMILEScopy InChI
Affinity DataIC50: 7.19E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279566(CHEMBL4164056)copy SMILEScopy InChI
Affinity DataIC50: 7.91E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279544(CHEBI:80907 | Sweroside)copy SMILEScopy InChI
Affinity DataIC50: 8.95E+4nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279555(CHEMBL4168853)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
TargetSignal transducer and activator of transcription 3(Homo sapiens (Human))
Beijing University of Chinese Medicine

Curated by ChEMBL
LigandPNGBDBM50279565(CHEMBL4169822)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of IL-6-Induced STAT3 activation (unknown origin) expressed in human HepG2 cells expressing pSTAT3-luciferase pre-incubated for 1 hr befor...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3Q11PubMed
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