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Found 116 with Last Name = 'murata' and Initial = 'm'
TargetGlucagon receptor(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50122102(3-Cyano-4-hydroxy-benzoic acid [1-(2,3,5,6-tetrame...)
Affinity DataIC50:  2.30nMAssay Description:Antagonist activity against human glucagon receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucagon receptor(Rattus norvegicus)
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50057796(CHEMBL3326188)
Affinity DataIC50:  5.30nMAssay Description:Inhibition of glucagon-induced glucagon receptor-mediated cAMP production in rat hepatocytes after 15 mins by cAMP dynamic2 assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067407((3R)-2'-(4-bromo-2-fluorobenzyl)-1'H,2H,5H-spiro[p...)
Affinity DataIC50:  15nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM16314(2-{[6-methoxy-5-(trifluoromethyl)naphthalen-1-yl]-...)
Affinity DataIC50:  15nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50009777((ponalrestat)[3-(4-Bromo-2-fluoro-benzyl)-4-oxo-3,...)
Affinity DataIC50:  21nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16499((2S)-2-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Affinity DataIC50:  23nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067390(2'-(3,4-dichlorobenzyl)spiro[tetrahydro-1H-pyrrole...)
Affinity DataIC50:  23nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16500((2S)-2-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Affinity DataIC50:  24nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16502((2S)-1-[(2S,3S)-2-{[(2S,3S)-3-(benzylcarbamoyl)oxi...)
Affinity DataIC50:  29nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
TargetBromodomain-containing protein 4(Homo sapiens (Human))
Mitsubishi Tanabe Pharma

Curated by ChEMBL
LigandPNGBDBM50151243(CHEMBL3771129)
Affinity DataIC50:  34nMAssay Description:Inhibition of Flag-tagged BRD4 (unknown origin)-biotinylated AcH4 (Lys5, 8, 12, 16) histone peptide binding expressed in CHO cells after 60 mins by T...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067379(2'-(3-chlorobenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  35nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067401(2'-(4-bromo-2-fluorobenzyl)-6'-chlorospiro[tetrahy...)
Affinity DataIC50:  35nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067409(2'-(3-bromobenzyl)spiro[tetrahydro-1H-pyrrole-3,4'...)
Affinity DataIC50:  37nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067391(2'-(2-chlorobenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  37nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16509((2S)-1-[(2S,3S)-3-methyl-2-{[(2S,3S)-3-(propylcarb...)
Affinity DataIC50:  38nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067396(2'-(4-chlorobenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  38nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067400(6'-bromo-2'-(4-bromo-2-fluorobenzyl)spiro[tetrahyd...)
Affinity DataIC50:  40nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16510((2S,3S)-3-[[(1S)-1-(isoamylcarbamoyl)-3-methyl-but...)
Affinity DataIC50:  40nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067375(2'-(4-chloro-2-fluorobenzyl)spiro[tetrahydro-1H-py...)
Affinity DataIC50:  41nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067376(2'-(4-bromo-2-fluorobenzyl)spiro[tetrahydro-1H-pyr...)
Affinity DataIC50:  45nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067382(2'-(4-methoxybenzyl)spiro[tetrahydro-1H-pyrrole-3,...)
Affinity DataIC50:  46nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067399(2'-(4-bromobenzyl)spiro[tetrahydro-1H-pyrrole-3,4'...)
Affinity DataIC50:  47nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067402(2'-(4-bromo-2-fluorobenzyl)-7'-chlorospiro[tetrahy...)
Affinity DataIC50:  50nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067395(6',7'-dibromo-2'-(4-bromo-2-fluorobenzyl)spiro[tet...)
Affinity DataIC50:  52nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067413(2'-(2-bromobenzyl)spiro[tetrahydro-1H-pyrrole-3,4'...)
Affinity DataIC50:  52nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067386(2'-(4-methylbenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  52nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067411(2'-(2-fluorobenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  61nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067387(2'-(2,4-difluorobenzyl)spiro[tetrahydro-1H-pyrrole...)
Affinity DataIC50:  72nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067414(2'-(4-trifluoromethylbenzyl)spiro[tetrahydro-1H-py...)
Affinity DataIC50:  80nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucagon receptor(Rattus norvegicus)
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50057824(CHEMBL3326175)
Affinity DataIC50:  87nMAssay Description:Displacement of [125I]glucagon from glucagon receptor in rat hepatocyte membranes after 30 mins by gamma-countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067394(2'-benzylspiro[tetrahydro-1H-pyrrole-3,4'-(1',2',3...)
Affinity DataIC50:  99nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067388(7'-bromo-2'-(4-bromo-2-fluorobenzyl)spiro[tetrahyd...)
Affinity DataIC50:  100nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067380(2'-(4-nitrobenzyl)spiro[tetrahydro-1H-pyrrole-3,4'...)
Affinity DataIC50:  110nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067381(2'-(3,4-dimethoxybenzyl)spiro[tetrahydro-1H-pyrrol...)
Affinity DataIC50:  110nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16508((2S)-1-[(2S,3S)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Affinity DataIC50:  120nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067404(2'-(4-fluorobenzyl)spiro[tetrahydro-1H-pyrrole-3,4...)
Affinity DataIC50:  120nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067398(CHEMBL133662 | [2-(3,4-Dichloro-benzyl)-1,3-dioxo-...)
Affinity DataIC50:  131nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067405(3-[2-(3,4-Dichloro-benzyl)-1,3-dioxo-1,2,3,4-tetra...)
Affinity DataIC50:  132nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067403(2'-(4-aminobenzyl)spiro[tetrahydro-1H-pyrrole-3,4'...)
Affinity DataIC50:  140nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucagon receptor(Rattus norvegicus)
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50057820(CHEMBL3326174)
Affinity DataIC50:  160nMAssay Description:Displacement of [125I]glucagon from glucagon receptor in rat hepatocyte membranes after 30 mins by gamma-countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067392(CHEMBL134089 | [2-(4-Bromo-2-fluoro-benzyl)-1,3-di...)
Affinity DataIC50:  165nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067397((3S)-2'-(4-bromo-2-fluorobenzyl)-1'H,2H,5H-spiro[p...)
Affinity DataIC50:  190nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067416(2'-phenylspiro[tetrahydro-1H-pyrrole-3,4'-(1',2',3...)
Affinity DataIC50:  200nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067408(7'-acetyl-2'-(4-bromo-2-fluorobenzyl)spiro[tetrahy...)
Affinity DataIC50:  210nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067385(2'-phenethylspiro[tetrahydro-1H-pyrrole-3,4'-(1',2...)
Affinity DataIC50:  270nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucagon receptor(Rattus norvegicus)
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50057813(CHEMBL3326173)
Affinity DataIC50:  270nMAssay Description:Displacement of [125I]glucagon from glucagon receptor in rat hepatocyte membranes after 30 mins by gamma-countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067406(2'-methylspiro[tetrahydro-1H-pyrrole-3,4'-(1',2',3...)
Affinity DataIC50:  280nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlucagon receptor(Homo sapiens (Human))
Dainippon Sumitomo Pharma

Curated by ChEMBL
LigandPNGBDBM50057796(CHEMBL3326188)
Affinity DataIC50:  292nMAssay Description:Inhibition of glucagon-induced glucagon receptor-mediated cAMP production in human hepatocytes after 15 mins by cAMP dynamic2 assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Sus scrofa)
Dainippon Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50067377(2'-(2,4-dimethoxybenzyl)spiro[tetrahydro-1H-pyrrol...)
Affinity DataIC50:  350nMAssay Description:In vitro inhibitory activity against aldose reductase in porcine lens.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Bos taurus (bovine))
Osaka University of Pharmaceutical Sciences

LigandPNGBDBM16501((2S)-2-[(2S,3R)-2-{[(2S,3S)-3-(ethoxycarbonyl)oxir...)
Affinity DataIC50:  410nMpH: 6.0 T: 2°CAssay Description:Inhibitory activities (IC50, concentration of 50% inhibition) of compounds for bovine CB in vitro were determined by monitoring the cleavage of fluor...More data for this Ligand-Target Pair
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