Compile Data Set for Download or QSAR
Report error Found 25 Enz. Inhib. hit(s) with all data for entry = 50035460
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028756BDBM50028756(2-Methyl-3-(4-pyridin-3-ylmethyl-phenyl)-acrylic a...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028764BDBM50028764(3-(4-Imidazol-1-ylmethyl-phenyl)-2-methyl-acrylic ...)
Affinity DataIC50: 4nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028761BDBM50028761(2-Bromo-3-(4-pyridin-3-ylmethyl-phenyl)-acrylic ac...)
Affinity DataIC50: 5nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028752BDBM50028752(2-(4-Pyridin-3-ylmethyl-benzylidene)-butyric acid;...)
Affinity DataIC50: 7nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028767BDBM50028767(3-(4-Pyridin-3-ylmethyl-phenyl)-acrylic acid; hydr...)
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028762BDBM50028762(2-Methyl-3-(5-pyridin-3-ylmethyl-thiophen-2-yl)-ac...)
Affinity DataIC50: 12nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028760BDBM50028760(3-(3-Methyl-4-pyridin-3-ylmethyl-phenyl)-but-2-eno...)
Affinity DataIC50: 18nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028772BDBM50028772(2-Methyl-3-(4-pyridin-3-ylmethyl-phenyl)-propionic...)
Affinity DataIC50: 20nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028758BDBM50028758(2-Methyl-3-[4-(1-pyridin-3-yl-ethyl)-phenyl]-acryl...)
Affinity DataIC50: 25nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 92497BDBM92497(CHEMBL542051 | Omega-imidazolyl octanoic acid)
Affinity DataIC50: 32nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028714BDBM50028714(7-Imidazol-1-yl-heptanoic acid; hydrochloride | CH...)
Affinity DataIC50: 39nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028774BDBM50028774(3-(5-Pyridin-3-ylmethyl-thiophen-2-yl)-acrylic aci...)
Affinity DataIC50: 47nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028759BDBM50028759(3-(4-Pyridin-3-ylmethyl-phenyl)-but-2-enoic acid; ...)
Affinity DataIC50: 56nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028755BDBM50028755(7-Pyridin-3-yl-heptanoic acid; hydrochloride | CHE...)
Affinity DataIC50: 68nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028773BDBM50028773(8-Pyridin-3-yl-octanoic acid; hydrochloride | CHEM...)
Affinity DataIC50: 76nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028754BDBM50028754(6-Pyridin-3-yl-hexanoic acid; hydrochloride | CHEM...)
Affinity DataIC50: 86nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028769BDBM50028769(3-(4-Pyridin-3-ylmethyl-phenyl)-propionic acid; hy...)
Affinity DataIC50: 210nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028757BDBM50028757(5-Pyridin-3-yl-pentanoic acid; hydrochloride | CHE...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028771BDBM50028771(2-Methyl-3-(4-pyridin-4-ylmethyl-phenyl)-acrylic a...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028770BDBM50028770(5-Pyridin-4-yl-pentanoic acid; hydrochloride | CHE...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028753BDBM50028753(7-Pyridin-4-yl-heptanoic acid; hydrochloride | CHE...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028766BDBM50028766(6-Pyridin-4-yl-hexanoic acid; hydrochloride | CHEM...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028768BDBM50028768(6-Imidazol-1-yl-hexanoic acid; hydrochloride | CHE...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50028763BDBM50028763(8-Pyridin-4-yl-octanoic acid; hydrochloride | CHEM...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed
TargetThromboxane-A synthase(Human)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 84684BDBM84684(CHEMBL543494 | 1-Subsituted 1H-imidazole, 21)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/12/2012
Entry Details Article
PubMed