Compile Data Set for Download or QSAR
Found 16 with Last Name = 'qin' and Initial = 'b'
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase Mer(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50090182(CHEMBL3581580)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+3nMAssay Description:Inhibition of human erythrocytes acetylcholinesterase after 30 mins using S-acetylthiocholine iodide substrate by spectrophotometry based Ellman meth...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2JH8PubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50090184(CHEMBL3581573)copy SMILEScopy InChI
Affinity DataIC50: 2.54E+4nMAssay Description:Inhibition of human erythrocytes acetylcholinesterase after 30 mins using S-acetylthiocholine iodide substrate by spectrophotometry based Ellman meth...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2JH8PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50090183(CHEMBL3581576)copy SMILEScopy InChI
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of human erythrocytes acetylcholinesterase after 30 mins using S-acetylthiocholine iodide substrate by spectrophotometry based Ellman meth...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2JH8PubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421320(CHEMBL2088175)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor TYRO3(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421322(CHEMBL2088178)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Tyro3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Beijing Institute of Pharmacology& Toxicology

Curated by ChEMBL
LigandPNGBDBM50421321(CHEMBL2088176)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of AxlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046QMPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50090185(CHEMBL3581572)copy SMILEScopy InChI
Affinity DataIC50: 3.72E+4nMAssay Description:Inhibition of human erythrocytes acetylcholinesterase after 30 mins using S-acetylthiocholine iodide substrate by spectrophotometry based Ellman meth...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2JH8PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Fudan University

Curated by ChEMBL
LigandPNGBDBM50118677(CHEMBL3617358)copy SMILEScopy InChI
Affinity DataEC50:  4.58E+4nMAssay Description:Agonist activity at ERbeta (248 to 510 amino acid residues) (unknown origin) assessed as induction of interaction with SRC1 after 24 hrs by yeast two...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3463PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Fudan University

Curated by ChEMBL
LigandPNGBDBM50118675(Isopaucifloral F)copy SMILEScopy InChI
Affinity DataEC50:  4.70E+4nMAssay Description:Agonist activity at ERbeta (248 to 510 amino acid residues) (unknown origin) assessed as induction of interaction with SRC1 after 24 hrs by yeast two...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3463PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Fudan University

Curated by ChEMBL
LigandPNGBDBM50118704(CHEMBL3617360)copy SMILEScopy InChI
Affinity DataEC50:  5.65E+3nMAssay Description:Agonist activity at ERbeta (248 to 510 amino acid residues) (unknown origin) assessed as induction of interaction with SRC1 after 24 hrs by yeast two...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3463PubMed