Compile Data Set for Download or QSAR
Report error Found 58 Enz. Inhib. hit(s) with all data for entry = 50027634
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275059BDBM50275059((Z)-1-(Benzo[b]thiophen-3-ylmethylene)-6-methyl-4-...)
Affinity DataIC50: 970nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275013BDBM50275013((Z)-1-((1H-Indol-2-yl)methylene)-6-methyl-4-thioxo...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274962BDBM50274962((Z)-1-((5-Methoxybenzofuran-2-yl)methylene)-6-meth...)
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275239BDBM50275239((Z)-6-Methyl-1-((5-methylfuran-2-yl)methylene)-4-t...)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274964BDBM50274964((Z)-1-((7-Methoxybenzofuran-2-yl)methylene)-6-meth...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275015BDBM50275015((Z)-1-((6-Methoxy-1H-indol-2-yl)methylene)-6-methy...)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275274BDBM50275274((Z)-6-Methyl-1-((5-phenylthiophen-2-yl)methylene)-...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275060BDBM50275060((Z)-1-[(4-Methoxy-1-benzothien-3-yl)methylene]-6-m...)
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275241BDBM50275241((Z)-6-Methyl-1-((5-phenylfuran-2-yl)methylene)-4-t...)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275134BDBM50275134((Z)-1-((1H-Indol-7-yl)methylene)-6-methyl-4-thioxo...)
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275098BDBM50275098((Z)-6-Methyl-1-((1-methyl-1H-indol-3-yl)methylene)...)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275240BDBM50275240((Z)-1-(Furan-2-ylmethylene)-6-methyl-4-thioxo-4,5-...)
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274991BDBM50274991((Z)-1-(Benzo[b]thiophen-2-ylmethylene)-6-methylfur...)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275014BDBM50275014((Z)-1-((5-Methoxy-1H-indol-2-yl)methylene)-6-methy...)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275094BDBM50275094((Z)-1-((6-Methoxybenzo[b]thiophen-3-yl)methylene)-...)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274829BDBM50274829((Z)-6-Methyl-1-((5-phenylthiophen-2-yl)methylene)f...)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274987BDBM50274987((Z)-1-((6-(Benzyloxy)-5-methoxybenzofuran-2-yl)met...)
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275093BDBM50275093((Z)-1-((5-Methoxybenzo[b]thiophen-3-yl)methylene)-...)
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274990BDBM50274990((Z)-1-((6-Methoxybenzo[b]thiophen-2-yl)methylene)-...)
Affinity DataIC50: 5.40E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275017BDBM50275017((Z)-1-((5-Fluoro-6-methoxy-1H-indol-3-yl)methylene...)
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274961BDBM50274961((Z)-1-((4-Methoxybenzofuran-2-yl)methylene)-6-meth...)
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275273BDBM50275273((Z)-6-Methyl-1-((5-methylthiophen-2-yl)methylene)-...)
Affinity DataIC50: 7.20E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274963BDBM50274963((Z)-1-((6-Methoxybenzofuran-2-yl)methylene)-6-meth...)
Affinity DataIC50: 7.20E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275095BDBM50275095((Z)-1-((5-Bromobenzo[b]thiophen-3-yl)methylene)-6-...)
Affinity DataIC50: 7.50E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274960BDBM50274960((Z)-1-(Benzofuran-2-ylmethylene)-6-methyl-4-thioxo...)
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275096BDBM50275096((Z)-1-(Benzo[b]thiophen-3-ylmethylene)-6-methylfur...)
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275242BDBM50275242((Z)-6-Methyl-1-(thiophen-2-ylmethylene)-4-thioxo-4...)
Affinity DataIC50: 8.60E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274988BDBM50274988((Z)-1-(Benzo[b]thiophen-2-ylmethylene)-6-methyl-4-...)
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274989BDBM50274989((Z)-1-((5-Methoxybenzo[b]thiophen-2-yl)methylene)-...)
Affinity DataIC50: 1.31E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275016BDBM50275016((Z)-1-((6-(Benzyloxy)-5-methoxy-1H-indol-2-yl)meth...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275056BDBM50275056((Z)-1-((5-(Benzyloxy)-1H-indol-2-yl)methylene)-6-m...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275058BDBM50275058((Z)-1-(Benzofuran-3-ylmethylene)-6-methyl-4-thioxo...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275057BDBM50275057((Z)-6-Methyl-1-((1-methyl-1H-indol-2-yl)methylene)...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275276BDBM50275276((Z)-1-((1H-Imidazol-2-yl)methylene)-6-methyl-4-thi...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275275BDBM50275275((Z)-1-((1H-Pyrrol-2-yl)methylene)-6-methyl-4-thiox...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275278BDBM50275278((Z)-1-Benzylidene-6-methyl-4-thioxo-4,5-dihydrofur...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275277BDBM50275277((Z)-6-Methyl-1-((1-methyl-1H-pyrrol-2-yl)methylene...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275313BDBM50275313((Z)-1-(4-Chlorobenzylidene)-6-methyl-4-thioxo-4,5-...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275279BDBM50275279((Z)-1-(4-Fluorobenzylidene)-6-methyl-4-thioxo-4,5-...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275315BDBM50275315((Z)-6-Methyl-4-thioxo-1-(4-(trifluoromethyl)benzyl...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275314BDBM50275314((Z)-6-Methyl-1-(4-methylbenzylidene)-4-thioxo-4,5-...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275317BDBM50275317((Z)-6-Methyl-4-thioxo-1-(4-(trifluoromethoxy)benzy...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275316BDBM50275316((Z)-1-(4-Methoxybenzylidene)-6-methyl-4-thioxo-4,5...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274825BDBM50274825((Z)-1-(4-(Dimethylamino)benzylidene)-6-methyl-4-th...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275318BDBM50275318((Z)-6-Methyl-1-(4-(methylthio)benzylidene)-4-thiox...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274827BDBM50274827((Z)-1-(Biphenyl-4-ylmethylene)-6-methyl-4-thioxo-4...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274826BDBM50274826((Z)-N-(4-((6-Methyl-3-oxo-4-thioxo-4,5-dihydrofuro...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274828BDBM50274828((Z)-6-Methyl-1-((5-methylfuran-2-yl)methylene)furo...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50274830BDBM50274830((Z)-1-((1H-Pyrrol-2-yl)methylene)-6-methylfuro[3,4...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetPerforin-1(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50275097BDBM50275097((Z)-1-((1H-Indol-3-yl)methylene)-6-methyl-4-thioxo...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant perforin-mediated lysis of human Jurkat T cells by 51Cr release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
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