Compile Data Set for Download or QSAR
Found 74 with Last Name = 'mahuran' and Initial = 'd'
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85134(Isofagomine derivative, 7)copy SMILEScopy InChI
Affinity DataKi:  0.0700nMpH: 7.0Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85134(Isofagomine derivative, 7)copy SMILEScopy InChI
Affinity DataKi:  0.200nMpH: 5.5Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383315(CHEMBL2029773)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383327(CHEMBL2029772)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383321(CHEMBL2029780)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383323(CHEMBL2029778)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383325(CHEMBL2029776)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50075408(5-(hydroxymethyl)piperidine-3,4-diol | CHEMBL34512...)copy SMILEScopy InChI
Affinity DataKi:  5nMpH: 7.0Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383324(CHEMBL2029777)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383319(CHEMBL2029782)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383328(CHEMBL2029771)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383322(CHEMBL2029779)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50075408(5-(hydroxymethyl)piperidine-3,4-diol | CHEMBL34512...)copy SMILEScopy InChI
Affinity DataKi:  23nMpH: 5.5Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383326(CHEMBL2029775)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383318(CHEMBL2029783)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383314(CHEMBL2029774)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85133(Isofagomine derivative, 10)copy SMILEScopy InChI
Affinity DataKi:  100nMpH: 5.5Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85133(Isofagomine derivative, 10)copy SMILEScopy InChI
Affinity DataKi:  110nMpH: 7.0Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383329(CHEMBL2029770)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383320(CHEMBL2029781)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85131(Isofagomine derivative, 6)copy SMILEScopy InChI
Affinity DataKi:  210nMpH: 7.0Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383317(CHEMBL2029784)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383316(CHEMBL2029785)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85132(Isofagomine derivative, 8)copy SMILEScopy InChI
Affinity DataKi:  600nMpH: 5.5Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85131(Isofagomine derivative, 6)copy SMILEScopy InChI
Affinity DataKi:  610nMpH: 5.5Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383330(CHEMBL2029769)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM85132(Isofagomine derivative, 8)copy SMILEScopy InChI
Affinity DataKi:  1.40E+3nMpH: 7.0Assay Description:Fluorescene-based assay using beta-glucocerebrosidase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD3Z3WPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50383331(CHEMBL2029768)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM50182798((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM68271(M-31850)copy SMILEScopy InChI
Affinity DataIC50: 600nMT: 2°CAssay Description:Enzyme assay based on 4-MU substrates with HTS to identify inhibitory compounds for Hex.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00W8PubMed
TargetCytosolic beta-glucosidase(Homo sapiens (Human))
University of British Columbia

Curated by ChEMBL
LigandPNGBDBM50383315(CHEMBL2029773)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human cytosolic beta-glucosidase using 4-methylumbelliferyl beta-D-glucopyranoside as substrate after 15 mins by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2639QSXPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMpH: 7.0Assay Description:Inhibition of human placental HexA using MUGS substrate incubated for 1 to 2 hrs at pH 7.0 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Genetics and Genome Biology, SickKids, PGCRL 686 Bay Street, Toronto, Ontario M5G 0A4, Canada.

Curated by ChEMBL
LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+3nMpH: 7.0Assay Description:Inhibition of human placental HexB using MUGS substrate incubated for 1 to 2 hrs at pH 7.0 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM68272(LU79953)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMT: 2°CAssay Description:Enzyme assay based on 4-MU substrates with HTS to identify inhibitory compounds for Hex.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00W8PubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM84610(5-(3,5-dichlorophenoxy)-N-(4-pyrdinyl)-2- furamide...)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMpH: 5.5 T: 2°CAssay Description:Beta-glucocerebrosidase (GCase) activity was measured by release of 4-methylumbelliferyl fluorophore from MUClc.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ0ZJKPubMed
TargetLysosomal acid glucosylceramidase(Homo sapiens (Human))
University of British Columbia

LigandPNGBDBM18046(5-((4-methylphenyl)thio)-quinazoline 2,4-diamine, ...)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+3nMpH: 5.5 T: 2°CAssay Description:Beta-glucocerebrosidase (GCase) activity was measured by release of 4-methylumbelliferyl fluorophore from MUClc.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JQ0ZJKPubMed
TargetBeta-galactosidase(Homo sapiens (Human))
Technische Universität Graz

Curated by ChEMBL
LigandPNGBDBM50246569(CHEMBL505422 | Methyl 6-[N2-dansyl-N6-(1,5-dideoxy...)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+3nMAssay Description:Inhibition of human lysosomal beta galactosidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DZ085JPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+3nMpH: 4.5Assay Description:Inhibition of HexA alpha G269S mutant in ATSD patient fibroblasts using MUGS substrate incubated for 1 to 2 hrs at pH 4.5 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 8.90E+3nMpH: 4.5Assay Description:Inhibition of human placental HexA using MUGS substrate incubated for 1 to 2 hrs at pH 4.5 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Genetics and Genome Biology, SickKids, PGCRL 686 Bay Street, Toronto, Ontario M5G 0A4, Canada.

Curated by ChEMBL
LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 9.10E+3nMpH: 4.5Assay Description:Inhibition of human placental HexB using MUGS substrate incubated for 1 to 2 hrs at pH 4.5 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18788(6-ethyl-5-phenylpyrimidine-2,4-diamine | CHEMBL221...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMpH: 7.0Assay Description:Inhibition of human placental HexA using MUGS substrate incubated for 1 to 2 hrs at pH 7.0 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMpH: 4.5Assay Description:Inhibition of HexA in normal human fibroblasts using MUGS substrate incubated for 1 to 2 hrs at pH 4.5 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit beta(Homo sapiens (Human))
Genetics and Genome Biology, SickKids, PGCRL 686 Bay Street, Toronto, Ontario M5G 0A4, Canada.

Curated by ChEMBL
LigandPNGBDBM18788(6-ethyl-5-phenylpyrimidine-2,4-diamine | CHEMBL221...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMpH: 7.0Assay Description:Inhibition of human placental HexB using MUGS substrate incubated for 1 to 2 hrs at pH 7.0 by spectrofluorometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM50089680(CHEMBL3577321)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human placental HexA using pNPGlcNAc substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha/beta(Homo sapiens (Human))
Genetics and Genome Biology, SickKids, PGCRL 686 Bay Street, Toronto, Ontario M5G 0A4, Canada.

Curated by ChEMBL
LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of beta-N-acetylhexosaminidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM68270(5141402)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMT: 2°CAssay Description:Enzyme assay based on 4-MU substrates with HTS to identify inhibitory compounds for Hex.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00W8PubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18512(5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine |...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human placental HexA using pNPGlcNAc substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM18780(6-ethyl-5-(4-methoxyphenyl)pyrimidine-2,4-diamine ...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of human placental HexA using pNPGlcNAc substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM50089676(CHEMBL3577317)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of human placental HexA using pNPGlcNAc substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28054CKPubMed
TargetBeta-hexosaminidase subunit alpha(Homo sapiens (Human))
Research Institute, Hospital for Sick Children

LigandPNGBDBM50106194(1,3-dioxo-1H-benz[de]isoquinoline | 1,8-Naphthalim...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMT: 2°CAssay Description:Enzyme assay based on 4-MU substrates with HTS to identify inhibitory compounds for Hex.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25B00W8PubMed
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