Compile Data Set for Download or QSAR
Found 37 with Last Name = 'ohi' and Initial = 'n'
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067631(3-(3-{[2-(Benzo[1,3]dioxol-5-yloxy)-ethyl]-methyl-...)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067622(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(3...)copy SMILEScopy InChI
Affinity DataIC50: 93nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50004704((+)-cis-Diltiazem | (2S,3S)-5-(2-(dimethylamino)et...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067624(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(3,4-...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067630(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(3...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50017896((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50017896((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067629(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-[3-(6,7-d...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067638(3-[3-(4-Benzyl-piperidin-1-yl)-propyl]-2-(3,5-di-t...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067637(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{[2-(4...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067632(3-{3-[4-(Benzothiazol-2-yl-methyl-amino)-piperidin...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067626(3-[3-(Benzo[1,3]dioxol-5-ylmethyl-methyl-amino)-pr...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043282(2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067620(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-{methy...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50017896((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50017896((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067639(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-hy...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067636(3-(3-{[3-(Benzo[1,3]dioxol-5-yloxy)-2-hydroxy-prop...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043282(2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067621(3-[3-(Benzyl-methyl-amino)-propyl]-2-(3,5-di-tert-...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067625(Benzothiazol-2-yl-{1-[4-(4-fluoro-phenoxy)-butyl]-...)copy SMILEScopy InChI
Affinity DataIC50: 760nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067635(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-et...)copy SMILEScopy InChI
Affinity DataIC50: 840nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50017896((E)-3-(4-Imidazol-1-ylmethyl-phenyl)-acrylic acid ...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067623(3-[3-(Cyclopropylmethyl-methyl-amino)-propyl]-2-(3...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043283(2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat plateletMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067633(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-dimeth...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043283(2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human microsomeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043283(2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human microsomeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043283(2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067640(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-di...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043283(2-Ethyl-4-pyridin-3-yl-2H-phthalazin-1-one | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067634(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-(3-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067628(2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3-{3-[(2-hy...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Rattus norvegicus)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043282(2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in rat whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043282(2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human microsomeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50067627(3-(3-Amino-propyl)-2-(3,5-di-tert-butyl-4-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+3nMAssay Description:In vitro inhibition of K+ induced contractions of the isolated rat aorta.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23N22JVPubMed
TargetThromboxane-A synthase(Homo sapiens (Human))
Chugai Pharmaceutical Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50043282(2-Methyl-4-thiazol-5-yl-2H-phthalazin-1-one | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+3nMAssay Description:Tested in vitro against TXA2 synthetase inhibitory activity in human whole bloodMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QJ7GBKPubMed