Compile Data Set for Download or QSAR
Found 1226 of ic50 data for polymerid = 1069,50001210
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50010960((E)-7-Phenyl-7-pyridin-3-yl-hept-6-enoic acid | 7-...)copy SMILEScopy InChI
Affinity DataIC50: 0.890nMAssay Description:In vitro inhibition of TXB2 production by incubating prostaglandin H2 with human platelet microsomes.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7P56PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50026486((Z)-7-Phenyl-7-pyridin-3-yl-hept-6-enoic acid | 7-...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Thromboxane A2 synthase inhibitory activity was measured from inhibition of thromboxane B2 production in human platelet microsomesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2MG7NT9PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50026486((Z)-7-Phenyl-7-pyridin-3-yl-hept-6-enoic acid | 7-...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibition of thromboxane synthase (TXA2) in human platelet microsomes [reduced formation of TXB2 from prostaglandin H2(PGH2)]More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X85ZHPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50110458(5-(Phenyl-pyridin-3-yl-methyleneaminooxy)-pentanoi...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of thromboxane synthase (TXA2) in human platelet microsomes [reduced formation of TXB2 from prostaglandin H2(PGH2)]More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X85ZHPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50043839((E)-6-[2-(4-Fluoro-benzenesulfonylamino)-indan-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition test of thromboxane A2 synthetase in human gel-filtered platelets.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SB44T4PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50109140(5-[1-Phenyl-1-pyridin-3-yl-meth-(Z)-ylideneaminoox...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:In vitro inhibition of TXB2 production by incubating prostaglandin H2 with human platelet microsomes.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7P56PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50109134(5-[1-Pyridin-3-yl-1-{3-[(3-pyridin-3-yl-1H-pyrrolo...)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:In vitro inhibition of TXB2 production by incubating prostaglandin H2 with human platelet microsomes.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7P56PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50109124(5-[1-(3-{[4-(2-Methyl-imidazo[4,5-c]pyridin-1-ylme...)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:In vitro inhibition of TXB2 production by incubating prostaglandin H2 with human platelet microsomes.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2ST7P56PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50038591(6-(5-Chloro-1-methyl-2-pyridin-3-yl-1H-indol-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Tested for 50% inhibition of thromboxane synthase (TxS) in human platelets (in vitro)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q280537CPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Medical Research Division of American Cyanamid Company

Curated by ChEMBL
LigandPNGBDBM50024903(6-Chloro-3-(4-imidazol-1-yl-butyl)-1H-quinazoline-...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Tested for inhibition of thromboxane synthetase from spontaneously hypertensive ratsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23T9HT6PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50003776(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4BG6
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50003776(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of the compound against thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53KS7
TargetThromboxane-A synthase(Rattus norvegicus)
Medical Research Division of American Cyanamid Company

Curated by ChEMBL
LigandPNGBDBM50024948(6-Chloro-3-(7-imidazol-1-yl-heptyl)-1H-quinazoline...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Tested for inhibition of thromboxane synthetase from spontaneously hypertensive ratsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23T9HT6PubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Medical Research Division of American Cyanamid Company

Curated by ChEMBL
LigandPNGBDBM50037039(2-Amino-5,7-dimethyl-4-pyridin-3-ylmethyl-benzothi...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibitory activity against the production of thromboxane B2 (TXB2) in glycogen-induced peritoneal cells of ratMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2WM1F2JPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50003776(8-(4-Chloro-benzenesulfonylamino)-4-(3-pyridin-3-y...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:In vitro inhibition of thromboxane synthasase in microsomal platelet preparationMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XS5TFKPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50043826(6-{4-[2-(4-Chloro-benzenesulfonylamino)-ethyl]-phe...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition test of thromboxane A2 synthetase in human gel-filtered platelets.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2SB44T4PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50020743(CHEMBL53346 | Sodium; (+)-7-(3-benzenesulfonylamin...)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibition of thromboxane A2 synthetase from human platelets by 1 uM of the compoundMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2G44P95PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50003797(8-(4-Chloro-benzenesulfonylamino)-4-[2-(pyridin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:In vitro inhibition of thromboxane synthasase in microsomal platelet preparationMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XS5TFKPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50072779((E)-7-{4-[4-(2-Phenoxy-ethylcarbamoyl)-oxazol-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:In vitro for inhibitory activity against thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V123Z8PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50072778((E)-7-(4-{4-[3-(4-Methoxy-phenyl)-propylcarbamoyl]...)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:In vitro for inhibitory activity against thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V123Z8PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50010960((E)-7-Phenyl-7-pyridin-3-yl-hept-6-enoic acid | 7-...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Activity against TXA2 synthase in bovine platelet microsomeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2639NTJPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50028756(2-Methyl-3-(4-pyridin-3-ylmethyl-phenyl)-acrylic a...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against Thromboxane synthetaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2FT8MMGPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50075618(6-{3-[2-cyano-1-cyclopentylamino-(E)-1-iminomethyl...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H41QMSPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50025953(6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4BG6
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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 the compound against thromboxane synthaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53KS7DrugBank
TargetThromboxane-A synthase(Rattus norvegicus)
Medical Research Division of American Cyanamid Company

Curated by ChEMBL
LigandPNGBDBM50024906(3-(3-Imidazol-1-yl-2-methyl-propyl)-6-methyl-1H-qu...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Tested for inhibition of thromboxane synthetase from spontaneously hypertensive ratsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23T9HT6PubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Medical Research Division of American Cyanamid Company

Curated by ChEMBL
LigandPNGBDBM50024934(7-Chloro-3-(3-imidazol-1-yl-2-methyl-propyl)-1H-qu...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Tested for inhibition of thromboxane synthetase from spontaneously hypertensive ratsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23T9HT6PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50075637(6-{3-[2-cyano-1-isopentylamino-(E)-1-iminomethylam...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H41QMSPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50075644((E)-6-[3-({[(E)-Benzenesulfonylimino]-tert-butylam...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H41QMSPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50075630(6-{3-[1-(1-adamantylamino)-2-cyano-(E)-1-iminometh...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H41QMSPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50075645(6-{3-[2-cyano-1-cyclohexylamino-(E)-1-iminomethyla...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro activity on thromboxane A2 synthase inhibition in gel filtered human platelets.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H41QMSPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM7962(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of TXA2 synthetase from human plateletsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W66JSZPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM7962(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of thromboxane TXA2 synthetase from human plateletsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2C8289WPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM7962(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against thromboxane A2 synthetaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DJ5DN7PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM7962(4-(2-Imidazol-1-yl-ethoxy)-benzoic acid; hydrochlo...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:In vitro inhibition of thromboxane synthase from human platelets.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2WQ02S2PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50008790(5-[Pyridin-4-yl-(3-trifluoromethyl-phenyl)-methyle...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Compound was evaluated in vitro for the inhibition of Thromboxane synthase using [14C]-arachidonic acid as radioligandMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BR8R47PubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

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))
Nikken Chemicals Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50025953(6-Imidazo[1,5-a]pyridin-5-yl-hexanoic acid | CGS-1...)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:In vitro inhibitory activity against thromboxane A2 synthetase with lysed human platelets as the enzyme source.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8ZKXPubMed
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