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TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113762(2-(hydroxymethyl)piperidine-3,4,5-triol;hydrochlor...)
Affinity DataIC50: 0.780nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113758(DGJ-pMe SPhT)
Affinity DataIC50: 1.40nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113762(2-(hydroxymethyl)piperidine-3,4,5-triol;hydrochlor...)
Affinity DataIC50: 3nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113758(DGJ-pMe SPhT)
Affinity DataIC50: 8.30nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113757(DGJ-pMe OPhT)
Affinity DataIC50: 16nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113759(DGJ-pF PhT)
Affinity DataIC50: 43nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113757(DGJ-pMe OPhT)
Affinity DataIC50: 74nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113759(DGJ-pF PhT)
Affinity DataIC50: 340nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113756(DGJ-NphT)
Affinity DataIC50: 370nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113756(DGJ-NphT)
Affinity DataIC50: 1.60E+3nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113760(pF PhIM-DGJ)
Affinity DataIC50: 2.18E+3nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197871(CHEMBL3979715)
Affinity DataIC50: 4.10E+3nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113761(DGJ-BnT)
Affinity DataIC50: 4.41E+3nMpH: 7.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197873(CHEMBL3974420)
Affinity DataIC50: 4.90E+3nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197869(CHEMBL3909220)
Affinity DataIC50: 6.80E+3nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197867(CHEMBL3980439)
Affinity DataIC50: 7.30E+3nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197870(CHEMBL3950752)
Affinity DataIC50: 8.60E+3nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113760(pF PhIM-DGJ)
Affinity DataIC50: 9.67E+3nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197866(CHEMBL3937138)
Affinity DataIC50: 1.24E+4nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetAlpha-galactosidase A(Human)
Tottori University , Yonago 683-8503, Japan

LigandPNGBDBM113761(DGJ-BnT)
Affinity DataIC50: 2.03E+4nMpH: 5.0Assay Description:For inhibition assay, 0.1% Triton X-100 extracts were mixed with 4-MU substrates ( 5 mM 4-MU α-ᴅ-galactopyranoside and 0.1 M N-acetyl-J...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/7/2014
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197871(CHEMBL3979715)
Affinity DataIC50: 4.00E+4nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197873(CHEMBL3974420)
Affinity DataIC50: 5.50E+4nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197869(CHEMBL3909220)
Affinity DataIC50: 5.60E+4nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197867(CHEMBL3980439)
Affinity DataIC50: 7.60E+4nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197870(CHEMBL3950752)
Affinity DataIC50: 9.20E+4nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197866(CHEMBL3937138)
Affinity DataIC50: 1.15E+5nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197874(CHEMBL3933048)
Affinity DataIC50: 1.21E+5nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197874(CHEMBL3933048)
Affinity DataIC50: 6.45E+5nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197872(CHEMBL3953477)
Affinity DataIC50: 7.88E+5nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197868(CHEMBL3931823)
Affinity DataIC50: 1.00E+6nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197872(CHEMBL3953477)
Affinity DataIC50: 1.00E+6nMpH: 5.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 5 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetLysosomal acid glucosylceramidase(Human)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50197868(CHEMBL3931823)
Affinity DataIC50: 1.00E+6nMpH: 7.0Assay Description:Inhibition of human beta-glucocerebrosidase using 4-methylumbelliferyl beta-D glycopyranoside as substrate at pH 7 by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,R201C](Human)
The University of Tokyo

LigandPNGBDBM228800(NOEV | Sapienic acid (SpA))
Affinity DataKi:  940nM ΔG°:  -35.8kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM228800(NOEV | Sapienic acid (SpA))
Affinity DataKi:  1.10E+3nM ΔG°:  -35.4kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,I51T](Human)
The University of Tokyo

LigandPNGBDBM228800(NOEV | Sapienic acid (SpA))
Affinity DataKi:  1.20E+3nM ΔG°:  -35.2kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetAlpha-galactosidase(Arabian coffee)
University of Seville

Curated by ChEMBL
LigandPNGBDBM50375511(CHEMBL406973)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of green coffee bean alpha-galactosidase using o-nitrophenyl alpha-D-galactopyranoside after 10 to 30 mins by spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetBeta-galactosidase(Escherichia coli (strain K12))
University of Seville

Curated by ChEMBL
LigandPNGBDBM50375511(CHEMBL406973)
Affinity DataKi:  4.30E+3nMAssay Description:Inhibition of Escherichia coli beta-galactosidase using o-nitrophenyl beta-D-galactopyranoside after 10 to 30 mins by spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/17/2018
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,I51T](Human)
The University of Tokyo

LigandPNGBDBM50163440((2R,3S,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataKi:  4.47E+4nM ΔG°:  -25.8kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetBeta-galactosidase [24-677,R201C](Human)
The University of Tokyo

LigandPNGBDBM50163440((2R,3S,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataKi:  4.90E+4nM ΔG°:  -25.6kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetBeta-galactosidase [24-677,R201C](Human)
The University of Tokyo

LigandPNGBDBM228802(5N,6S-(N'-butyliminomethylidene)-6-thio-1-deox...)
Affinity DataKi:  5.33E+4nM ΔG°:  -25.4kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM50163440((2R,3S,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataKi:  6.18E+4nM ΔG°:  -25.0kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM228802(5N,6S-(N'-butyliminomethylidene)-6-thio-1-deox...)
Affinity DataKi:  6.83E+4nM ΔG°:  -24.7kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,I51T](Human)
The University of Tokyo

LigandPNGBDBM228802(5N,6S-(N'-butyliminomethylidene)-6-thio-1-deox...)
Affinity DataKi:  6.88E+4nM ΔG°:  -24.7kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM228803(5N,6S-(N'-butyliminomethylidene)-6-thiogalacto...)
Affinity DataKi:  2.53E+5nM ΔG°:  -21.4kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,I51T](Human)
The University of Tokyo

LigandPNGBDBM228803(5N,6S-(N'-butyliminomethylidene)-6-thiogalacto...)
Affinity DataKi:  3.20E+5nM ΔG°:  -20.8kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,R201C](Human)
The University of Tokyo

LigandPNGBDBM228803(5N,6S-(N'-butyliminomethylidene)-6-thiogalacto...)
Affinity DataKi:  3.20E+5nM ΔG°:  -20.7kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,I51T](Human)
The University of Tokyo

LigandPNGBDBM228804(N-(N'-butylthiocarbamoyl)-1-deoxygalactonojiri...)
Affinity DataKi:  3.29E+5nM ΔG°:  -20.7kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM228804(N-(N'-butylthiocarbamoyl)-1-deoxygalactonojiri...)
Affinity DataKi:  3.73E+5nM ΔG°:  -20.4kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677,R201C](Human)
The University of Tokyo

LigandPNGBDBM228804(N-(N'-butylthiocarbamoyl)-1-deoxygalactonojiri...)
Affinity DataKi:  3.88E+5nM ΔG°:  -20.3kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
TargetBeta-galactosidase [24-677](Human)
The University of Tokyo

LigandPNGBDBM228805(Galactose)
Affinity DataKi:  4.14E+6nM ΔG°:  -14.1kJ/molepH: 4.5 T: 2°CAssay Description:β-Gal activity was measured by using 4-methylumbelliferyll-β-D-galactopyranoside in buffer B (0.15 M sodium citrate, pH 4.5, and 0.2 M NaCl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/30/2017
Entry Details Article
PubMed
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