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Found 70 with Last Name = 'kuromiya' and Initial = 'a'
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35276(tripeptide-based inhibitor, 14s)
Affinity DataIC50:  6.60nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35275(tripeptide-based inhibitor, 14r)
Affinity DataIC50:  6.60nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35257(tripeptide-based inhibitor, 14a)
Affinity DataIC50:  7.60nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35261(tripeptide-based inhibitor, 14d)
Affinity DataIC50:  14nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More 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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35269(tripeptide-based inhibitor, 14l)
Affinity DataIC50:  17nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35274(tripeptide-based inhibitor, 14q)
Affinity DataIC50:  20nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35273(tripeptide-based inhibitor, 14p)
Affinity DataIC50:  21nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35268(tripeptide-based inhibitor, 14k)
Affinity DataIC50:  23nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35259(tripeptide-based inhibitor, 14b)
Affinity DataIC50:  24nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35260(tripeptide-based inhibitor, 14c)
Affinity DataIC50:  27nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35263(tripeptide-based inhibitor, 14f)
Affinity DataIC50:  27nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35277(tripeptide-based inhibitor, 14t)
Affinity DataIC50:  28nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35279(AE-3763 | tripeptide-based inhibitor, 14v)
Affinity DataIC50:  29nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35271(tripeptide-based inhibitor, 14n)
Affinity DataIC50:  30nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35262(tripeptide-based inhibitor, 14e)
Affinity DataIC50:  33nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35266(tripeptide-based inhibitor, 14i)
Affinity DataIC50:  35nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...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
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
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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35265(tripeptide-based inhibitor, 14h)
Affinity DataIC50:  42nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35264(tripeptide-based inhibitor, 14g)
Affinity DataIC50:  43nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35267(tripeptide-based inhibitor, 14j)
Affinity DataIC50:  47nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...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
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35270(tripeptide-based inhibitor, 14m)
Affinity DataIC50:  62nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Dainippon Sumitomo Pharma

LigandPNGBDBM35272(tripeptide-based inhibitor, 14o)
Affinity DataIC50:  62nMpH: 7.5 T: 2°CAssay Description:To evaluate inhibitory effect of test compound, HNE was preincubated with each compound in the assay solution at 37 deg C for 4 min. The reaction was...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
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
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
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