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Found 10 Enz. Inhib. hit(s) with all data for entry = 50013898
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM16314(2-{[6-methoxy-5-(trifluoromethyl)naphthalen-1-yl]-...)
Affinity DataIC50:  400nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135849(2,3,4-trichloro-6-(3,4,5-trichloro-2-hydroxyphenox...)
Affinity DataIC50:  3.20E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135852(2,3,4-tribromo-6-(3,4-dibromo-5-fluoro-2-hydroxyph...)
Affinity DataIC50:  3.20E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM16312((4S)-6-fluoro-2,3-dihydrospiro[1-benzopyran-4,4'-i...)
Affinity DataIC50:  3.60E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135854(2,4-Dibromo-6-(3,4,5-tribromo-2-hydroxy-phenoxy)-b...)
Affinity DataIC50:  4.40E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135850(2,3,4,5-Tetrabromo-6-(3,4,5-tribromo-2-hydroxy-phe...)
Affinity DataIC50:  5.50E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135853(2,3,4-tribromo-6-(3,4,5-tribromo-2-hydroxyphenoxy)...)
Affinity DataIC50:  5.70E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135851(2,3,4,5-tetrabromo-6-(3,5-dibromo-2-hydroxy-phenox...)
Affinity DataIC50:  6.40E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135856(6-(2-Amino-3,4,5-tribromo-phenoxy)-2,3,4-tribromo-...)
Affinity DataIC50:  8.90E+3nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Instituto Biomar

Curated by ChEMBL
LigandPNGBDBM50135855(CHEMBL358713 | [2,3,4,5-Tetrabromo-6-(3,5-dibromo-...)
Affinity DataIC50:  2.50E+4nMAssay Description:In vitro inhibitory activity against recombinant human aldose reductase (ALR2) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed