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Found 38 with Last Name = 'ho' and Initial = 'cw'
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36548(N-[1-(7-{bis[(4-methoxyphenyl)methyl]amino}heptyl)...)
Affinity DataKi:  0.690nM ΔG°:  -53.2kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36547(N-[4,5-dihydroxy-6-(hydroxymethyl)-1-(7-{[(4-metho...)
Affinity DataKi:  1.20nM ΔG°:  -51.8kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36546(N-[1-(7-aminoheptyl)-4,5-dihydroxy-6-(hydroxymethy...)
Affinity DataKi:  2.10nM ΔG°:  -50.4kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36549(N-{7-[5-acetamido-3,4-dihydroxy-2-(hydroxymethyl)p...)
Affinity DataKi:  26.7nM ΔG°:  -44.0kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM50182804(2-ACETAMIDO-1,2-DIDEOXYNOJIRMYCIN | CHEMBL382689 |...)
Affinity DataKi:  540nM ΔG°:  -36.4kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36550(N-[1-(7-azidoheptyl)-4,5-dihydroxy-6-(hydroxymethy...)
Affinity DataKi:  1.70E+3nM ΔG°:  -33.5kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM50182804(2-ACETAMIDO-1,2-DIDEOXYNOJIRMYCIN | CHEMBL382689 |...)
Affinity DataKi:  2.36E+4nM ΔG°:  -26.9kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36547(N-[4,5-dihydroxy-6-(hydroxymethyl)-1-(7-{[(4-metho...)
Affinity DataKi:  1.02E+5nM ΔG°:  -23.2kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36546(N-[1-(7-aminoheptyl)-4,5-dihydroxy-6-(hydroxymethy...)
Affinity DataKi:  1.08E+5nM ΔG°:  -23.0kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36549(N-{7-[5-acetamido-3,4-dihydroxy-2-(hydroxymethyl)p...)
Affinity DataKi:  1.45E+5nM ΔG°:  -22.3kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36550(N-[1-(7-azidoheptyl)-4,5-dihydroxy-6-(hydroxymethy...)
Affinity DataKi:  1.55E+5nM ΔG°:  -22.1kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein O-GlcNAcase(Homo sapiens (Human))
Academia Sinica

LigandPNGBDBM36548(N-[1-(7-{bis[(4-methoxyphenyl)methyl]amino}heptyl)...)
Affinity DataKi:  1.76E+5nM ΔG°:  -21.8kJ/molepH: 4.25 T: 2°CAssay Description:Enzyme inhibition activity assay using 4-methylumbelliferyl N-acetylglucosamine (MUG) as substrate.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFarnesyl pyrophosphate synthase(Homo sapiens (Human))
Korea University

Curated by ChEMBL
LigandPNGBDBM50247920(Alendronate Sodium | Binosto | Fosamax | G-704650 ...)
Affinity DataIC50:  460nMAssay Description:Inhibition of recombinant human farnesyl diphosphate synthase in expressed in Escherichia coli using GPP and [1-14C]IPP as substrate incubated for 15...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsopentenyl-diphosphate Delta-isomerase 1(Rattus norvegicus)
Korea University

Curated by ChEMBL
LigandPNGBDBM50247920(Alendronate Sodium | Binosto | Fosamax | G-704650 ...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of isopentenyl diphosphate isomerase in Sprague-Dawley rat liver S100 fraction preincubated for 10 min followed by MVA addition by HPLC an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFarnesyl pyrophosphate synthase(Rattus norvegicus)
Korea University

Curated by ChEMBL
LigandPNGBDBM50247920(Alendronate Sodium | Binosto | Fosamax | G-704650 ...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of farnesyl diphosphate synthase in Sprague-Dawley rat liver S100 fraction using MVA as substrate preincubated for 10 min followed by MVA ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFarnesyl pyrophosphate synthase(Mus musculus)
Korea University

Curated by ChEMBL
LigandPNGBDBM50247920(Alendronate Sodium | Binosto | Fosamax | G-704650 ...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of farnesyl diphosphate synthase in Balb/C mouse osteoclast assessed as reduction in [3H]MVL incorporation into prenylated proteins preinc...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFarnesyl pyrophosphate synthase(Mus musculus)
Korea University

Curated by ChEMBL
LigandPNGBDBM50247920(Alendronate Sodium | Binosto | Fosamax | G-704650 ...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of farnesyl diphosphate synthase in Balb/C mouse osteoclast assessed as reduction in [3H]MVL incorporation into nonsaponifiable lipids pre...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394346(CHEMBL2159605)
Affinity DataEC50:  1.10E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50085045(5-((4-((6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-...)
Affinity DataEC50:  720nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394341(CHEMBL465800)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394342(CHEMBL458899)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394343(CHEMBL516827)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394344(CHEMBL2159607)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394345(CHEMBL2159606)
Affinity DataEC50:  3.31E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394346(CHEMBL2159605)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50371235(CIPROFIBRATE)
Affinity DataEC50:  900nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394341(CHEMBL465800)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394342(CHEMBL458899)
Affinity DataEC50:  4.29E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394343(CHEMBL516827)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394344(CHEMBL2159607)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394345(CHEMBL2159606)
Affinity DataEC50: >5.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394346(CHEMBL2159605)
Affinity DataEC50:  4.71E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394344(CHEMBL2159607)
Affinity DataEC50:  3.01E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50085041(2-(4-(3-(4-acetyl-3-hydroxy-2-propylphenoxy)propox...)
Affinity DataEC50:  650nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394342(CHEMBL458899)
Affinity DataEC50:  1.56E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394341(CHEMBL465800)
Affinity DataEC50:  2.31E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394343(CHEMBL516827)
Affinity DataEC50:  2.93E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50394345(CHEMBL2159606)
Affinity DataEC50:  1.31E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta (delta) ligand binding domain transfected in human HepG2 cells after 20 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed