Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067631 (3-(3-{[2-(Benzo[1,3]dioxol-5-yloxy)-ethyl]-methyl-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 62 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067622 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(3...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 93 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50004704 ((+)-cis-Diltiazem | (2S,3S)-5-(2-(dimethylamino)et...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars | Article PubMed | n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067624 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(3,4-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067630 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(3...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50017896 ((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50017896 ((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067629 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-[3-(6,7-d...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067638 (3-[3-(4-Benzyl-piperidin-1-yl)-propyl]-2-(3,5-di-t...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067637 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(4...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067632 (3-{3-[4-(Benzothiazol-2-yl-methyl-amino)-piperidin...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067626 (3-[3-(Benzo[1,3]dioxol-5-ylmethyl-methyl-amino)-pr...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50043282 (2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067620 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{methy...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50017896 ((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50017896 ((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067639 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-hy...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 420 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067636 (3-(3-{[3-(Benzo[1,3]dioxol-5-yloxy)-2-hydroxy-prop...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043282 (2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 500 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067621 (3-[3-(Benzyl-methyl-amino)-propyl]-2-(3,5-di-tert-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 600 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067625 (Benzothiazol-2-yl-{1-[4-(4-fluoro-phenoxy)-butyl]-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 760 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067635 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-et...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 840 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50017896 ((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars | PubMed | n/a | n/a | 900 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067623 (3-[3-(Cyclopropylmethyl-methyl-amino)-propyl]-2-(3...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50043283 (2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat platelet | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067633 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-dimeth...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043283 (2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human microsome | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043283 (2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human microsome | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50043283 (2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067640 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-di...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043283 (2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067634 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-methyl...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067628 (2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-hy...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 3.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Rattus norvegicus) | BDBM50043282 (2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...) | Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 3.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in rat whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043282 (2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 3.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human microsome | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Voltage-dependent L-type calcium channel subunit alpha-1C (RAT) | BDBM50067627 (3-(3-Amino-propyl)-2-(3,5-di-tert-butyl-4-hydroxy-...) | PDB UniProtKB/SwissProt GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description In vitro inhibition of K+ induced contractions of the isolated rat aorta. | J Med Chem 41: 4309-16 (1998) Article DOI: 10.1021/jm980335f BindingDB Entry DOI: 10.7270/Q23N22JV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Thromboxane-A synthase (Homo sapiens (Human)) | BDBM50043282 (2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...) | KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | PubMed | n/a | n/a | 8.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chugai Pharmaceutical Company, Ltd. Curated by ChEMBL | Assay Description Tested in vitro against TXA2 synthetase inhibitory activity in human whole blood | J Med Chem 36: 4061-8 (1994) BindingDB Entry DOI: 10.7270/Q2QJ7GBK | |||||||||||
More data for this Ligand-Target Pair |