Compile Data Set for Download or QSAR
Found 38 with Last Name = 'boswell' and Initial = 'c'
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003792(8-(4-Fluoro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003784(8-(4-Chloro-benzenesulfonylamino)-4-[3-(4-methyl-p...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003780(4-(3-Pyridin-3-yl-propyl)-8-(toluene-4-sulfonylami...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003803(8-(Naphthalene-2-sulfonylamino)-4-(3-pyridin-3-yl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003801(4-(3-Pyridin-3-yl-propyl)-8-(4-trifluoromethyl-ben...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003776(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003781(CHEMBL341686 | [5-(4-Chloro-benzenesulfonylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003796(8-(4-Chloro-benzenesulfonylamino)-4-[3-(1-oxy-pyri...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003799(8-(4-Chloro-benzenesulfonylamino)-2-methyl-4-(3-py...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003795(5-[1-Pyridin-3-yl-1-(3-trifluoromethyl-phenyl)-met...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMedDrugBank
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003797(8-(4-Chloro-benzenesulfonylamino)-4-[2-(pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003800(8-(4-Methoxy-benzenesulfonylamino)-4-(3-pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003798(8-(4-Chloro-benzenesulfonylamino)-4-(3-imidazol-1-...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003789(8-(4-Methanesulfonyl-benzenesulfonylamino)-4-(3-py...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003777(8-(4-Chloro-benzenesulfonylamino)-2-(5-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003794(8-(4-Azido-benzenesulfonylamino)-4-(3-pyridin-3-yl...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003787(4-Chloro-N-{8-pyridin-3-yl-5-[2-(5H-tetrazol-5-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003804(7-(4-Chloro-benzenesulfonylamino)-3-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003790(CHEMBL136880 | Potassium; 8-(4-chloro-benzenesulfo...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003793(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003779(8-(4-Chloro-benzenesulfonylamino)-6-pyridin-3-ylme...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50280260(7-{4-[3-(4-Chloro-benzenesulfonylamino)-propyl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibitory concentration of the compound against thromboxane synthase enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZF2
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003791(CHEMBL343535 | [5-(4-Chloro-benzenesulfonylamino)-...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003783(8-(4-Chloro-benzenesulfonylamino)-2,2-dimethyl-4-(...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003776(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003773(8-(4-Chloro-benzenesulfonylamino)-5-(2-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003786(8-(4-Chloro-benzenesulfonylamino)-4-(2-imidazol-1-...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50280261(6-{4-[2-(4-Chloro-benzenesulfonylamino)-ethyl]-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibitory concentration of the compound against thromboxane synthase enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZF2
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003788(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50280262(6-{4-[(4-Chloro-benzenesulfonylamino)-methyl]-pyri...)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibitory concentration of the compound against thromboxane synthase enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZF2
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003782(4-Chloro-N-[5-(3-hydroxy-propyl)-8-pyridin-3-yl-oc...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50280263(7-{4-[2-(4-Chloro-benzenesulfonylamino)-ethyl]-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibitory concentration of the compound against thromboxane synthase enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZF2
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003802(6-(4-Chloro-benzenesulfonylamino)-2-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50280259(6-{4-[3-(4-Chloro-benzenesulfonylamino)-propyl]-py...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibitory concentration of the compound against thromboxane synthase enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZF2
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003775(8-(4-Chloro-benzenesulfonylamino)-3-(4-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003785(CHEMBL137187 | N-[5-(4-Chloro-benzenesulfonylamino...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:In vitro inhibition of Thromboxane A2 synthaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2F47N3WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003759(8-(4-Chloro-benzenesulfonylamino)-7-pyridin-3-yl-o...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
CIBA-GEIGY Corporation

Curated by ChEMBL
LigandPNGBDBM50003778(8-(4-Chloro-benzenesulfonylamino)-8-pyridin-3-yl-o...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:The compound was tested in vitro for its inhibitory activity against thromboxane synthase A2 (TXA2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2JW8CVBPubMed