Compile Data Set for Download or QSAR
Found 6 with Last Name = 'gromer' and Initial = 's'
TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
UMR 8525 CNRS-Université Lille II-Institut Pasteur de Lille

Curated by ChEMBL
LigandPNGBDBM50176071(2-(2-Amino-ethylamino)-N-(7-{2-[N'-(5-nitro-furan-...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibitory concentration against human glutathione reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN73F9PubMed
TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
UMR 8525 CNRS-Université Lille II-Institut Pasteur de Lille

Curated by ChEMBL
LigandPNGBDBM50121447(5-Nitro-furan-2-carboxylic acid N'-(2-naphthalen-2...)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibitory concentration against human glutathione reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN73F9PubMed
TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
UMR 8525 CNRS-Université Lille II-Institut Pasteur de Lille

Curated by ChEMBL
LigandPNGBDBM50241461(3,7-bis(dimethylamino)phenothiazin-5-ium chloride ...)copy SMILEScopy InChI
Affinity DataIC50: 1.64E+4nMpH: 6.9Assay Description:Inhibition of human recombinant glutathione reductase at pH 6.9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5F0TPubMed
TargetThioredoxin reductase 1, cytoplasmic(Homo sapiens (Human))
Biochemie-Zentrum der Universit£t Heidelberg

Curated by ChEMBL
LigandPNGBDBM50241461(3,7-bis(dimethylamino)phenothiazin-5-ium chloride ...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMpH: 7.4Assay Description:Inhibition of human recombinant TrxR1 at pH 7.4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5F0TPubMed
TargetDihydrolipoyl dehydrogenase(Plasmodium falciparum)
Biochemie-Zentrum der Universit£t Heidelberg

Curated by ChEMBL
LigandPNGBDBM50241461(3,7-bis(dimethylamino)phenothiazin-5-ium chloride ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMpH: 7.3Assay Description:Inhibition of Plasmodium falciparum recombinant dihydrolipoamide dehydrogenase at pH 7.3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5F0TPubMed
TargetDihydrolipoyl dehydrogenase, mitochondrial(Sus scrofa)
Biochemie-Zentrum der Universit£t Heidelberg

Curated by ChEMBL
LigandPNGBDBM50241461(3,7-bis(dimethylamino)phenothiazin-5-ium chloride ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMpH: 7.3Assay Description:Inhibition of pig recombinant dihydrolipoamide dehydrogenase at pH 7.3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5F0TPubMed