Compile Data Set for Download or QSAR
Found 15 with Last Name = 'chen' and Initial = 'xs'
TargetUrease subunit beta(Helicobacter pylori (strain ATCC 700392 / 26695) (...)
Liaoning Normal University

Curated by ChEMBL
LigandPNGBDBM50485420(CHEMBL2058477)copy SMILEScopy InChI
Affinity DataIC50: 2.73E+4nMAssay Description:Inhibition of Helicobacter pylori urease assessed as ammonia production preincubated for 3 hrs measured by indophenol methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ68X2PubMed
TargetUrease subunit beta(Helicobacter pylori (strain ATCC 700392 / 26695) (...)
Liaoning Normal University

Curated by ChEMBL
LigandPNGBDBM50485419(2,5-Biscyclopentylamino-[1,4]Benzoquinone | CHEMBL...)copy SMILEScopy InChI
Affinity DataIC50: 3.54E+4nMAssay Description:Inhibition of Helicobacter pylori urease assessed as ammonia production preincubated for 3 hrs measured by indophenol methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ68X2PubMed
TargetUrease subunit beta(Helicobacter pylori (strain ATCC 700392 / 26695) (...)
Liaoning Normal University

Curated by ChEMBL
LigandPNGBDBM50485418(2,5-Biscyclohexylamino-[1,4]Benzoquinone | CHEMBL2...)copy SMILEScopy InChI
Affinity DataIC50: 4.15E+4nMAssay Description:Inhibition of Helicobacter pylori urease assessed as ammonia production preincubated for 3 hrs measured by indophenol methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ68X2PubMed
TargetUrease subunit beta(Helicobacter pylori (strain ATCC 700392 / 26695) (...)
Liaoning Normal University

Curated by ChEMBL
LigandPNGBDBM50099857(ACETOHYDROXAMIC ACID (AHA) | AHA | Acethydroxamsae...)copy SMILEScopy InChI
Affinity DataIC50: 4.63E+4nMAssay Description:Inhibition of Helicobacter pylori urease assessed as ammonia production preincubated for 3 hrs measured by indophenol methodMore data for this Ligand-Target Pair
LigandPNGBDBM4814(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)copy SMILEScopy InChI
Affinity DataKd:  2.00E+3nMAssay Description:Binding affinity to human DDR1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))TBA
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)copy SMILEScopy InChI
Affinity DataKd:  31nMAssay Description:Binding affinity to human FLT1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMedDrugBank
TargetPlatelet-derived growth factor receptor alpha(Homo sapiens (Human))TBA
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)copy SMILEScopy InChI
Affinity DataKd:  62nMAssay Description:Binding affinity to human PDGFRAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)copy SMILEScopy InChI
Affinity DataKd:  62nMAssay Description:Binding affinity to human RETMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMedDrugBank
TargetTyrosine-protein kinase ABL2(Homo sapiens (Human))TBA
LigandPNGBDBM13530(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)copy SMILEScopy InChI
Affinity DataKd:  10nMAssay Description:Binding affinity to human ABL2More data for this Ligand-Target Pair
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))TBA
LigandPNGBDBM13530(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)copy SMILEScopy InChI
Affinity DataKd: >1.00E+4nMAssay Description:Binding affinity to human FLT3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))TBA
LigandPNGBDBM13530(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)copy SMILEScopy InChI
Affinity DataKd: >1.00E+4nMAssay Description:Binding affinity to human FLT4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
LigandPNGBDBM16673(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)copy SMILEScopy InChI
Affinity DataKd:  28nMAssay Description:Binding affinity to human CSF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
LigandPNGBDBM13216(BMS-354825 | CHEMBL1421 | DASATINIB | N-(2-Chloro-...)copy SMILEScopy InChI
Affinity DataKd:  0.580nMAssay Description:Binding affinity to human CSF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))TBA
LigandPNGBDBM50564768(Azaepothilone b | BMS 247550-01 | BMS-247550 | BMS...)copy SMILES
Affinity DataKd:  337nMAssay Description:Binding affinity to human recombinant Bcl-2 expressed in Escherichia coli by Surface plasmon resonance assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed
TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))TBA
LigandPNGBDBM4814(CHEMBL535 | N-[2-(diethylamino)ethyl]-5-[(Z)-(5-fl...)copy SMILEScopy InChI
Affinity DataKd:  100nMAssay Description:Binding affinity to human NTRK1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RN3CK9PubMed