Found 181 with Last Name = 'okazaki' and Initial = 's' TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
The University of Tokyo
Curated by ChEMBL
The University of Tokyo
Curated by ChEMBL
Affinity DataKi: 10nMAssay Description:Displacement of [3H]rosiglitazone from PPARgamma (unknown origin)More data for this Ligand-Target Pair
3D Structure (crystal)TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 0.700nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 1.20nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
Affinity DataIC50: 1.60nMAssay Description:Displacement of [125I]His3-MePhe7)-NKB from human NK3R expressed in CHO cell membranes by topcounting methodMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 2.60nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 2.60nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 2.60nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 2.70nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 3nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 3nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 3.5nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 3.60nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 3.80nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 3.80nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.90nMAssay Description:Displacement of [125I]His3-MePhe7)-NKB from human NK3R expressed in CHO cell membranes by topcounting methodMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 3.90nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 4nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 4.10nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
Affinity DataIC50: 4.60nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 4.70nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 4.80nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 5nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit alpha-2/delta(Rattus norvegicus (Rat))
Kyowa Hakko Kirin Co., Ltd.
US Patent
Kyowa Hakko Kirin Co., Ltd.
US Patent
Affinity DataIC50: 5.20nMT: 2°CAssay Description:A test compound (20 μL) diluted to 5 times of the final concentration with Binding buffer, [3H]-gabapentin diluted to 100 nmol/L with binding buff...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 5.40nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 5.60nMAssay Description:Displacement of [125I]His3-MePhe7)-NKB from human NK3R expressed in CHO cell membranes by topcounting methodMore data for this Ligand-Target Pair
Affinity DataIC50: 6nMAssay Description:Displacement of [125I]His3-MePhe7)-NKB from human NK3R expressed in CHO cell membranes by topcounting methodMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 6.70nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 7.90nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 8nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 8nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.40nMAssay Description:Displacement of [125I]His3-MePhe7)-NKB from human NK3R expressed in CHO cell membranes by topcounting methodMore data for this Ligand-Target Pair
Affinity DataIC50: 8.80nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 8.90nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.5nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.60nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 9.80nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.80nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 9.80nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 11nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 11nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Inhibition of full length recombinant C-terminal His-tagged human ACC2 expressed in baculovirus infected sf9 cells using acetyl-CoA as substrate afte...More data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Affinity DataIC50: 11nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Toray Industries, Inc.
Curated by ChEMBL
Toray Industries, Inc.
Curated by ChEMBL
Affinity DataIC50: 12nMAssay Description:Inhibition of mouse 11beta-HSD1 expressed in HEK293 cells using cortisone and NADPH as substrate by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 12nMAssay Description:Inhibition of GST-tagged human CK2alpha' (1 to 350 residues) using CK2tide as substrate incubated for 1 hr by off-chip mobility shift assayMore data for this Ligand-Target Pair
