Compile Data Set for Download or QSAR
Found 22 with Last Name = 'ganem' and Initial = 'b'
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096495(CHEMBL85161 | N-{3-[Bis-(3-phenyl-propyl)-amino]-p...)copy SMILEScopy InChI
Affinity DataKi:  151nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201010(((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  236nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096500(CHEMBL86281 | N,N'-Bis-(3-phenyl-propyl)-N,N'-bis-...)copy SMILEScopy InChI
Affinity DataKi:  614nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201013(((2S,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096491(CHEMBL85189 | N-(3-Amino-propyl)-N,N'-bis-(3-pheny...)copy SMILEScopy InChI
Affinity DataKi:  1.38E+3nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096496(CHEMBL62048 | N,N'-Bis-(3-amino-propyl)-N,N'-bis-(...)copy SMILEScopy InChI
Affinity DataKi:  3.48E+3nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096493(CHEMBL82641 | N,N'-Bis-(3-phenyl-propyl)-N-[3-(3-p...)copy SMILEScopy InChI
Affinity DataKi:  3.50E+3nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096492(CHEMBL84221 | N-{3-[Bis-(3-phenyl-propyl)-amino]-p...)copy SMILEScopy InChI
Affinity DataKi:  3.62E+3nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096501(CHEMBL85198 | N*1*-(3-Phenyl-propyl)-N*1*-[3-(3-ph...)copy SMILEScopy InChI
Affinity DataKi:  4.67E+3nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201015(((2R,3aR,4R,6R,6aS)-6-(hydroxymethyl)-4-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  8.03E+3nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096494(CHEMBL310207 | N,N'-Bis-{3-[bis-(3-phenyl-propyl)-...)copy SMILEScopy InChI
Affinity DataKi:  1.03E+4nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096498(CHEMBL86096 | N,N'-Bis-[3-(3-phenyl-propylamino)-p...)copy SMILEScopy InChI
Affinity DataKi:  1.23E+4nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096499(CHEMBL85964 | N*1*-(3-Amino-propyl)-N*1*-(3-phenyl...)copy SMILEScopy InChI
Affinity DataKi:  1.41E+4nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201012(((2R,3aR,4S,6R,6aR)-4-(hydroxymethyl)-6-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi:  3.34E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetTrypanothione reductase(Trypanosoma cruzi)
Indiana State University

Curated by ChEMBL
LigandPNGBDBM50096497(CHEMBL85779 | N-(3-Amino-propyl)-N'-[3-(3-phenyl-p...)copy SMILEScopy InChI
Affinity DataKi:  3.76E+4nMAssay Description:Tested for binding affinity against trypanothione reductase from Trypanosoma cruziMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FQ9VVVPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201011(2-((2R,3aR,4R,6R,6aR)-4-(hydroxymethyl)-6-(5-methy...)copy SMILEScopy InChI
Affinity DataKi:  4.35E+4nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetThymidine phosphorylase(Homo sapiens (Human))
Attenuon, LLC

Curated by ChEMBL
LigandPNGBDBM50201014(((2S,3aR,4R,6R,6aS)-6-(hydroxymethyl)-4-(5-methyl-...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+5nMAssay Description:Inhibition of human thymidine phosphorylase by continuous spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FB52KFPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50175526((7-Oxo-cyclohept-1-enyl)-acetic acid (E)-propenyl ...)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF-7piGST cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24749FBPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50175526((7-Oxo-cyclohept-1-enyl)-acetic acid (E)-propenyl ...)copy SMILEScopy InChI
Affinity DataIC50: 1.08E+4nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF7wt cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24749FBPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50122751((6-Oxo-cyclohex-1-enyl)-acetic acid (E)-propenyl e...)copy SMILEScopy InChI
Affinity DataIC50: 1.32E+4nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF-7piGST cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24749FBPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University of Maryland

Curated by ChEMBL
LigandPNGBDBM50122751((6-Oxo-cyclohex-1-enyl)-acetic acid (E)-propenyl e...)copy SMILEScopy InChI
Affinity DataIC50: 2.96E+4nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF7wt cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24749FBPubMed
TargetEnvelope glycoprotein gp160(Human immunodeficiency virus type 1 group M subtyp...)
Cornell University

Curated by ChEMBL
LigandPNGBDBM50403756(CHEMBL2029048)copy SMILEScopy InChI
Affinity DataKd:  11nMAssay Description:Binding affinity towards HIV glycoprotein gp120More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JQ108SPubMed