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Found 15 with Last Name = 'miranda' and Initial = 'c'
TargetLow molecular weight phosphotyrosine protein phosphatase(Mus musculus)
University Of Campinas

Curated by ChEMBL
LigandPNGBDBM50096252(CHEMBL3594198)
Affinity DataKi:  4.70E+4nMAssay Description:Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLow molecular weight phosphotyrosine protein phosphatase(Mus musculus)
University Of Campinas

Curated by ChEMBL
LigandPNGBDBM50096253(CHEMBL3593255)
Affinity DataKi:  1.24E+5nMAssay Description:Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlkaline phosphatase, placental type(Homo sapiens (Human))
University Of Campinas

Curated by ChEMBL
LigandPNGBDBM50080274(Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...)
Affinity DataKi:  5.80E+5nMAssay Description:Inhibition of human placental alkaline phosphatase using p-nitrophenyl phosphate substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEctonucleotide pyrophosphatase/phosphodiesterase family member 3(Bos taurus)
University Of Campinas

Curated by ChEMBL
LigandPNGBDBM50080274(Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...)
Affinity DataKi:  1.40E+6nMAssay Description:Inhibition of bovine intestinal 5'-nucleotide phosphodiesterase using 4-nitrophenyl phenylphosphonate substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
University Of Campinas

Curated by ChEMBL
LigandPNGBDBM50080274(Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...)
Affinity DataKi:  3.00E+6nMAssay Description:Inhibition of PTP1B (unknown origin) using nPP substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  42nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  120nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM50535444(CHEMBL4463058)
Affinity DataIC50:  190nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM50535445(CHEMBL4455730)
Affinity DataIC50:  215nMAssay Description:Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM50535444(CHEMBL4463058)
Affinity DataIC50:  316nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Bras£Lia

Curated by ChEMBL
LigandPNGBDBM50535445(CHEMBL4455730)
Affinity DataIC50:  775nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada

Curated by ChEMBL
LigandPNGBDBM50389793(CHEMBL2070385)
Affinity DataIC50:  8.92E+4nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada

Curated by ChEMBL
LigandPNGBDBM50389791(CHEMBL2070383)
Affinity DataIC50:  9.66E+4nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada

Curated by ChEMBL
LigandPNGBDBM50389792(CHEMBL2070384)
Affinity DataIC50:  1.55E+5nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetExtracellular superoxide dismutase [Cu-Zn](Homo sapiens (Human))
Universidad De Granada

Curated by ChEMBL
LigandPNGBDBM50389790(CHEMBL2070382)
Affinity DataIC50:  2.74E+5nMAssay Description:Inhibition of human erythrocyte Cu-Zn SOD by NBT reduction assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed