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Found 101 with Last Name = 'pirrung' and Initial = 'mc'
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129580(3-[4,6-Dichloro-7-(3-methyl-but-2-enyl)-1H-indol-3...)
Affinity DataKi:  430nMAssay Description:Inhibitory constant of compound against Cell division cycle 25B was determined using mFP as a substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129576(2,5-Dihydroxy-3-[7-(3,7,11-trimethyl-dodeca-2,6,10...)
Affinity DataKi:  640nMAssay Description:Inhibitory constant of compound against Cell division cycle 25 was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataKi:  640nMAssay Description:Inhibitory constant of compound against Cell division cycle 25B was determined using mFP as a substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-aminocyclopropane-1-carboxylate oxidase 1(Malus domestica (Apple) (Pyrus malus))
Duke University

LigandPNGBDBM36630(N-hydroxy aminoisobutryic acid)
Affinity DataKi:  1.30E+4nMAssay Description:Enzyme inhibition assay using ethylene-forming enzyme (EFE).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129575(2,5-Dihydroxy-3-(1H-indol-3-yl)-[1,4]benzoquinone ...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibitory constant of compound against Cdc25B phosphatase was determined using mFP as a substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-aminocyclopropane-1-carboxylate oxidase 1(Malus domestica (Apple) (Pyrus malus))
Duke University

LigandPNGBDBM36632(N-Hydroxyaminocyclobutanecarboxylic acid)
Affinity DataKi:  1.80E+4nMAssay Description:Enzyme inhibition assay using ethylene-forming enzyme (EFE).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-aminocyclopropane-1-carboxylate oxidase 1(Malus domestica (Apple) (Pyrus malus))
Duke University

LigandPNGBDBM36629(Aminoisobutyric (AIB))
Affinity DataKi:  1.50E+5nMAssay Description:Enzyme inhibition assay using ethylene-forming enzyme (EFE).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target1-aminocyclopropane-1-carboxylate oxidase 1(Malus domestica (Apple) (Pyrus malus))
Duke University

LigandPNGBDBM36631(Aminocyclobutanecarboxylic acid (ACBC))
Affinity DataKi:  2.20E+5nMAssay Description:Enzyme inhibition assay using ethylene-forming enzyme (EFE).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129583(3-[7-(3,7-Dimethyl-octa-2,6-dienyl)-1H-indol-3-yl]...)
Affinity DataIC50:  1.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  1.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  1.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129580(3-[4,6-Dichloro-7-(3-methyl-but-2-enyl)-1H-indol-3...)
Affinity DataIC50:  2.30E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129585(3-(7-Benzyl-1H-indol-3-yl)-2,5-dihydroxy-[1,4]benz...)
Affinity DataIC50:  2.30E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129585(3-(7-Benzyl-1H-indol-3-yl)-2,5-dihydroxy-[1,4]benz...)
Affinity DataIC50:  2.30E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129576(2,5-Dihydroxy-3-[7-(3,7,11-trimethyl-dodeca-2,6,10...)
Affinity DataIC50:  2.40E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129576(2,5-Dihydroxy-3-[7-(3,7,11-trimethyl-dodeca-2,6,10...)
Affinity DataIC50:  2.40E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129572(3-(1H-Benzo[g]indol-3-yl)-2,5-dihydroxy-[1,4]benzo...)
Affinity DataIC50:  2.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129577(2,5-Dihydroxy-3-(7-phenyl-1H-indol-3-yl)-[1,4]benz...)
Affinity DataIC50:  2.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129577(2,5-Dihydroxy-3-(7-phenyl-1H-indol-3-yl)-[1,4]benz...)
Affinity DataIC50:  2.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Duke University

Curated by ChEMBL
LigandPNGBDBM50074938((R)-2-(4-Methoxy-phenyl)-4,5-dihydro-oxazole-4-car...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of E. coli LpxC(UDP-3-O-[R-3-hydroxymyristoyl]-GlcNAc deacetylase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129579(2,5-Dihydroxy-3-[7-(2-methyl-benzyl)-1H-indol-3-yl...)
Affinity DataIC50:  3.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129576(2,5-Dihydroxy-3-[7-(3,7,11-trimethyl-dodeca-2,6,10...)
Affinity DataIC50:  3.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  3.90E+3nMAssay Description:Inhibitory concentration of compound against mutant M532A of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129581(3-[6-Chloro-7-(3-methyl-but-2-enyl)-1H-indol-3-yl]...)
Affinity DataIC50:  4.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Duke University

Curated by ChEMBL
LigandPNGBDBM50118596((R/S)-[3-(4-Methoxy-phenyl)-4,5-dihydro-isoxazol-5...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of E. coli LpxC(UDP-3-O-[R-3-hydroxymyristoyl]-GlcNAc deacetylase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  4.10E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129584(3-(7-Benzyloxy-1H-indol-3-yl)-2,5-dihydroxy-[1,4]b...)
Affinity DataIC50:  4.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129584(3-(7-Benzyloxy-1H-indol-3-yl)-2,5-dihydroxy-[1,4]b...)
Affinity DataIC50:  4.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129582(2,5-Dihydroxy-3-(7-propyl-1H-indol-3-yl)-[1,4]benz...)
Affinity DataIC50:  4.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129586(3-(6-Chloro-1H-indol-3-yl)-2,5-dihydroxy-[1,4]benz...)
Affinity DataIC50:  4.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Duke University

Curated by ChEMBL
LigandPNGBDBM50409600(CHEMBL2111931)
Affinity DataIC50:  4.37E+3nMAssay Description:Inhibition of E. coli LpxC(UDP-3-O-[R-3-hydroxymyristoyl]-GlcNAc deacetylase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129580(3-[4,6-Dichloro-7-(3-methyl-but-2-enyl)-1H-indol-3...)
Affinity DataIC50:  5.00E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129571(3-(5-Benzyloxy-1H-indol-3-yl)-2,5-dihydroxy-[1,4]b...)
Affinity DataIC50:  5.50E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  5.60E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129569(3-(5-Bromo-1H-indol-3-yl)-2,5-dihydroxy-[1,4]benzo...)
Affinity DataIC50:  5.80E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  6.40E+3nMAssay Description:Inhibitory concentration of compound against mutant WT of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibitory concentration of compound against mutant M531A of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibitory concentration of compound against mutant E478Q of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129584(3-(7-Benzyloxy-1H-indol-3-yl)-2,5-dihydroxy-[1,4]b...)
Affinity DataIC50:  6.90E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129581(3-[6-Chloro-7-(3-methyl-but-2-enyl)-1H-indol-3-yl]...)
Affinity DataIC50:  7.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129570(3-(7-tert-Butyl-1H-indol-3-yl)-2,5-dihydroxy-[1,4]...)
Affinity DataIC50:  7.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129570(3-(7-tert-Butyl-1H-indol-3-yl)-2,5-dihydroxy-[1,4]...)
Affinity DataIC50:  7.20E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129588(2,5-Dihydroxy-3-(5-methyl-1H-indol-3-yl)-[1,4]benz...)
Affinity DataIC50:  8.10E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25A was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129580(3-[4,6-Dichloro-7-(3-methyl-but-2-enyl)-1H-indol-3...)
Affinity DataIC50:  8.60E+3nMAssay Description:Inhibitory concentration of compound against Cell division cycle 25B was determined using CDK2-p-TpY/Cyclin A as a substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129580(3-[4,6-Dichloro-7-(3-methyl-but-2-enyl)-1H-indol-3...)
Affinity DataIC50:  8.80E+3nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129583(3-[7-(3,7-Dimethyl-octa-2,6-dienyl)-1H-indol-3-yl]...)
Affinity DataIC50:  1.00E+4nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibitory concentration of compound against mutant R492L of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 3(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129581(3-[6-Chloro-7-(3-methyl-but-2-enyl)-1H-indol-3-yl]...)
Affinity DataIC50:  1.10E+4nMAssay Description:Eight point inhibitory concentration against Cell division cycle 25 degree C was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-3-O-acyl-N-acetylglucosamine deacetylase(Escherichia coli)
Duke University

Curated by ChEMBL
LigandPNGBDBM50118597((R/S)-Thioacetic acid S-{2-[3-(4-methoxy-phenyl)-4...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of E. coli LpxC(UDP-3-O-[R-3-hydroxymyristoyl]-GlcNAc deacetylase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Duke University

Curated by ChEMBL
LigandPNGBDBM50129574(2,5-Dihydroxy-3-[7-(3-methyl-but-2-enyl)-1H-indol-...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibitory concentration of compound against mutant R544L of Cell division cycle 25B was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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