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Found 65 with Last Name = 'tysoe' and Initial = 'c'
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383315(CHEMBL2029773)
Affinity DataKi:  0.400nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50254115(CHEMBL4080589)
Affinity DataKi:  1nMAssay Description:Competitive inhibition of recombinant beta-glucocerebrosidase (unknown origin) using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50018014(CHEMBL3289676)
Affinity DataKi:  1nMAssay Description:Inhibition of human lysosomal beta-glucocerebrosidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM223314(YPYSCWARHVRIREN | piHA-D1)
Affinity DataKi:  1nMpH: 7.0Assay Description:The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383327(CHEMBL2029772)
Affinity DataKi:  1.80nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50315250((2R,3S,4S,5R)-2-nonylpiperidine-3,4,5-triol | CHEM...)
Affinity DataKi:  2.20nMAssay Description:Inhibition of human lysosomal beta-glucocerebrosidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM223315(YPYSCWVRHSDPHKF | piHA-D3)
Affinity DataKi:  2.70nMpH: 7.0Assay Description:The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383321(CHEMBL2029780)
Affinity DataKi:  3nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383323(CHEMBL2029778)
Affinity DataKi:  4nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383325(CHEMBL2029776)
Affinity DataKi:  4.40nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Bos taurus (Bovine))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254109(CHEMBL4069909)
Affinity DataKi:  5.30nMAssay Description:Competitive inhibition of Bovine liver beta-galactosidase using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubated for up to 5 mins be...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383324(CHEMBL2029777)
Affinity DataKi:  6nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM223316(YPYSCWVRH | piHA-Dm)
Affinity DataKi:  7nMpH: 7.0Assay Description:The release of 2-chloro-4-nitrophenol resulting from the HPA-catalyzed hydrolysis of 2-chloro-4-nitrophenyl a-maltotrioside (CNPG3) was monitored at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50018018(CHEMBL3289679)
Affinity DataKi:  7.5nMAssay Description:Inhibition of human lysosomal beta-glucocerebrosidase using 2,4-dinitrophenyl-beta-D-glucopyranoside as substrate by UV spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163646(Montbretin A (MbA))
Affinity DataKi:  8.10nM ΔG°:  -47.0kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163647(MbA-G (1))
Affinity DataKi:  9.10nM ΔG°:  -46.7kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383319(CHEMBL2029782)
Affinity DataKi:  12nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383328(CHEMBL2029771)
Affinity DataKi:  18nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383322(CHEMBL2029779)
Affinity DataKi:  19nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by Dixon an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50254109(CHEMBL4069909)
Affinity DataKi:  19nMAssay Description:Competitive inhibition of recombinant beta-glucocerebrosidase (unknown origin) using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163648(MbA-R (2))
Affinity DataKi:  21.3nM ΔG°:  -44.5kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383326(CHEMBL2029775)
Affinity DataKi:  29nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383318(CHEMBL2029783)
Affinity DataKi:  30nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163649(MbA-RX (3))
Affinity DataKi:  42.4nM ΔG°:  -42.8kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383314(CHEMBL2029774)
Affinity DataKi:  76nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163650(MbA-GR (4))
Affinity DataKi:  79.3nM ΔG°:  -41.2kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163651(MbA-GRX (5) | mini-MbA)
Affinity DataKi:  93.3nM ΔG°:  -40.8kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
TargetBeta-galactosidase(Bos taurus (Bovine))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254116(CHEMBL4083115)
Affinity DataKi:  110nMAssay Description:Competitive inhibition of Bovine liver beta-galactosidase using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubated for up to 5 mins be...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Bos taurus (Bovine))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254117(CHEMBL4061246)
Affinity DataKi:  130nMAssay Description:Competitive inhibition of Bovine liver beta-galactosidase using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubated for up to 5 mins be...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383329(CHEMBL2029770)
Affinity DataKi:  180nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383320(CHEMBL2029781)
Affinity DataKi:  200nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383317(CHEMBL2029784)
Affinity DataKi:  250nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Homo sapiens (Human))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254109(CHEMBL4069909)
Affinity DataKi:  290nMAssay Description:Competitive inhibition of human fibroblast lysosomal beta-galactosidase using 4-methylumbelliferyl-beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383316(CHEMBL2029785)
Affinity DataKi:  450nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Homo sapiens (Human))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50358321(CHEMBL1922579 | CHEMBL1922581)
Affinity DataKi:  510nMAssay Description:Competitive inhibition of human fibroblast lysosomal beta-galactosidase using 4-methylumbelliferyl-beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163652(MbA-C (6))
Affinity DataKi:  730nM ΔG°:  -35.6kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Bos taurus (Bovine))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50358321(CHEMBL1922579 | CHEMBL1922581)
Affinity DataKi:  873nMAssay Description:Competitive inhibition of Bovine liver beta-galactosidase using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubated for up to 5 mins be...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383330(CHEMBL2029769)
Affinity DataKi:  1.10E+3nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50182798((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of human lysosomal beta-glucocerebrosidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163653(MbA-CG (7))
Affinity DataKi:  2.24E+3nM ΔG°:  -32.8kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383331(CHEMBL2029768)
Affinity DataKi:  2.70E+3nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50182798((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Affinity DataKi:  2.80E+3nMpH: 5.0Assay Description:Competitive inhibition of wild type human glucocerebrosidase using 2,4-dinitrophenyl beta-D-glucopyranoside as substrate after 3 mins by Dixon and Li...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Homo sapiens (Human))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254118(CHEMBL4090899)
Affinity DataKi:  9.20E+3nMAssay Description:Competitive inhibition of human fibroblast lysosomal beta-galactosidase using 4-methylumbelliferyl-beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50254117(CHEMBL4061246)
Affinity DataKi:  1.03E+4nMAssay Description:Competitive inhibition of recombinant beta-glucocerebrosidase (unknown origin) using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50254116(CHEMBL4083115)
Affinity DataKi:  1.07E+4nMAssay Description:Competitive inhibition of recombinant beta-glucocerebrosidase (unknown origin) using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubate...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucosidase(Agrobacterium tumefaciens)
Technical University Graz

Curated by ChEMBL
LigandPNGBDBM18351((2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-tr...)
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of Agrobacterium sp. beta glucosidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Homo sapiens (Human))
The University of Tokyo

LigandPNGBDBM163656(3-O-(6-(4-(Caffeamidomethyl)-triazolyl)hexyl)querc...)
Affinity DataKi:  1.39E+4nM ΔG°:  -28.2kJ/moleT: 2°CAssay Description:Inhibitor concentrations varied from 0.25 to 5 times the Ki value in 50 mM sodium phosphate, 100 mM sodium chloride buffer, pH 7.0, at 30 °C. 2-Chlor...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-galactosidase(Bos taurus (Bovine))
Graz University of Technology

Curated by ChEMBL
LigandPNGBDBM50254118(CHEMBL4090899)
Affinity DataKi:  3.10E+4nMAssay Description:Competitive inhibition of Bovine liver beta-galactosidase using 4-nitrophenyl beta-D-galactopyranoside as substrate pre-incubated for up to 5 mins be...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University Of British Columbia

Curated by ChEMBL
LigandPNGBDBM50018016(CHEMBL3289677)
Affinity DataKi:  3.40E+4nMAssay Description:Inhibition of human lysosomal beta-glucocerebrosidase using 2,4-dinitrophenyl-beta-D-glucopyranoside as substrate by UV spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucosidase(Agrobacterium tumefaciens)
Technical University Graz

Curated by ChEMBL
LigandPNGBDBM50018018(CHEMBL3289679)
Affinity DataKi:  3.60E+4nMAssay Description:Inhibition of Agrobacterium sp. beta glucosidase using 2,4-dinitrophenyl-beta-D-glucopyranoside as substrate measured for 3 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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