Compile Data Set for Download or QSAR
Found 62 with Last Name = 'pinto' and Initial = 'bm'
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330326((4S,5R,6R)-5-Acetylamino-4-guanidino-6-((1R,3R)-1,...)copy SMILEScopy InChI
Affinity DataKi:  0.160nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343682(((1S,5R,6R)-6-acetamido-3-carboxy-5-(pentan-3-ylox...)copy SMILEScopy InChI
Affinity DataKi:  0.460nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343681((3S,4R,5R)-4-Acetamido-3-amino-5-(1-ethylpropoxy)c...)copy SMILEScopy InChI
Affinity DataKi:  1.5nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetSucrase-isomaltase, intestinal(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327504(1,4-Dideoxy-1,4-[[2S,3S,4R,5S]-2,4,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  7nMAssay Description:Inhibition of human recombinant C-terminal Sucrase-isomaltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327503((1R,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)-1-((...)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Inhibition of human recombinant N-terminal domain of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ0411PubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330961((2R,3S,4S)-1-((2S,3S,4R,5R,6S)-2,3,4,5,6,7-hexahyd...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330954(CHEMBL1276973 | de-O-sulfonated kotalanol)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetSucrase-isomaltase, intestinal(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327504(1,4-Dideoxy-1,4-[[2S,3S,4R,5S]-2,4,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  35nMAssay Description:Inhibition of human recombinant N-terminal Sucrase-isomaltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327502((1R,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)-1-((...)copy SMILEScopy InChI
Affinity DataKi:  43nMAssay Description:Inhibition of human N-terminal maltase-glucoamylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327502((1R,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)-1-((...)copy SMILEScopy InChI
Affinity DataKi:  43nMAssay Description:Inhibition of human recombinant N-terminal domain of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ0411PubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330960((2R,3R,4R)-1-((2R,3R,4S,5R,6S)-2,3,4,5,6,7-hexahyd...)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343684((3S,4R,5R)-4-Acetamido-5-(1-ethyl-propoxy)-3-[4-(1...)copy SMILEScopy InChI
Affinity DataKi:  72nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330959(CHEMBL1277153)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50316180((1S,2R,3S,4S)-1-{(1S)-2-[(2R,3S,4S)-3,4-dihydroxy-...)copy SMILEScopy InChI
Affinity DataKi:  100nMAssay Description:Inhibition of recombinant human maltase glucoamylase N-terminal catalytic domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8Z5JPubMed
TargetSucrase-isomaltase, intestinal(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327502((1R,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)-1-((...)copy SMILEScopy InChI
Affinity DataKi:  103nMAssay Description:Inhibition of human recombinant C-terminal Sucrase-isomaltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343685((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(1-...)copy SMILEScopy InChI
Affinity DataKi:  130nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50316181((1S,2R,3S,4R)-1-{(1S)-2-[(2R,3S,4S)-3,4-dihydroxy-...)copy SMILEScopy InChI
Affinity DataKi:  130nMAssay Description:Inhibition of recombinant human maltase glucoamylase N-terminal catalytic domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8Z5JPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327501(CHEMBL1258528 | ponkoranol)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Inhibition of human recombinant N-terminal domain of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ0411PubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50316179((1S,2R,3R,4S)-1-{(1S)-2-[(2R,3S,4S)-3,4-dihydroxy-...)copy SMILEScopy InChI
Affinity DataKi:  190nMAssay Description:Inhibition of recombinant human maltase glucoamylase N-terminal catalytic domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8Z5JPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50316179((1S,2R,3R,4S)-1-{(1S)-2-[(2R,3S,4S)-3,4-dihydroxy-...)copy SMILEScopy InChI
Affinity DataKi:  190nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50316178(1,4-Dideoxy-1,4-[[2S,3S,4R,5R,6R-2,4,5,6,7-pentahy...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human maltase glucoamylase N-terminal catalytic domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22B8Z5JPubMed
TargetSucrase-isomaltase, intestinal(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327502((1R,2R,3S,4S)-3,4-dihydroxy-2-(hydroxymethyl)-1-((...)copy SMILEScopy InChI
Affinity DataKi:  302nMAssay Description:Inhibition of human recombinant N-terminal Sucrase-isomaltase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343683((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(3-...)copy SMILEScopy InChI
Affinity DataKi:  460nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327504(1,4-Dideoxy-1,4-[[2S,3S,4R,5S]-2,4,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Inhibition of human recombinant N-terminal domain of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ0411PubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327504(1,4-Dideoxy-1,4-[[2S,3S,4R,5S]-2,4,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Inhibition of human recombinant N-terminal maltase-glucoamylase by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50327504(1,4-Dideoxy-1,4-[[2S,3S,4R,5S]-2,4,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Inhibition of human N-terminal maltase-glucoamylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q81DHZPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330955((1S,2S)-3-[(2R,3S,4S)-3,4-dihydroxy-2-(hydroxymeth...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50242271((2R,3R,4R,5S)-1-(2-hydroxyethyl)-2-(hydroxymethyl)...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343686((3S,4R,5R)-4-acetamido-5-(pentan-3-yloxy)-3-(4-phe...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330957(7'-[(1,5-Dideoxy-1,5-imino-D-glucitol)-5-N-ammoniu...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330956(7'-[(1,5-Dideoxy-1,5-imino-D-glucitol)-5-N-ammoniu...)copy SMILEScopy InChI
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343689((3S,4R,5R)-4-acetamido-3-(4-((8R,9S,13S,14S,17S)-3...)copy SMILEScopy InChI
Affinity DataKi:  5.80E+3nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM4706((2R,3R,4S)-3-acetamido-4-hydroxy-2-[(1R,2R)-1,2,3-...)copy SMILEScopy InChI
Affinity DataKi:  5.90E+3nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343690((4R,5R)-4-acetamido-3-(4-(2-hydroxypropan-2-yl)-1H...)copy SMILEScopy InChI
Affinity DataKi:  1.90E+4nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343680((4R,5R)-4-acetamido-5-(pentan-3-yloxy)-3-(4-phenet...)copy SMILEScopy InChI
Affinity DataKi:  6.00E+4nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetMaltase-glucoamylase(Homo sapiens (Human))
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50330958((2R,3R,4R,5R,6S)-1-((2R,3R,4R)-3,4-dihydroxy-2-(hy...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+4nMAssay Description:Inhibition of human recombinant N-terminal subunit of maltase-glucoamylase after 60 mins by glucose oxidase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4RZHPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343687((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(1-...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetNeuraminidase(Influenza A virus)
Simon Fraser University

Curated by ChEMBL
LigandPNGBDBM50343688((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(1-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of influenza A nuraminidase N1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75K5BPubMed
TargetSialidase-4(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM4706((2R,3R,4S)-3-acetamido-4-hydroxy-2-[(1R,2R)-1,2,3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of human NEU4 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM4706((2R,3R,4S)-3-acetamido-4-hydroxy-2-[(1R,2R)-1,2,3-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343689((3S,4R,5R)-4-acetamido-3-(4-((8R,9S,13S,14S,17S)-3...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+5nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343690((4R,5R)-4-acetamido-3-(4-(2-hydroxypropan-2-yl)-1H...)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+5nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-4(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343689((3S,4R,5R)-4-acetamido-3-(4-((8R,9S,13S,14S,17S)-3...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+5nMAssay Description:Inhibition of human NEU4 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-4(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343681((3S,4R,5R)-4-Acetamido-3-amino-5-(1-ethylpropoxy)c...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU4 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-4(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343680((4R,5R)-4-acetamido-5-(pentan-3-yloxy)-3-(4-phenet...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU4 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343681((3S,4R,5R)-4-Acetamido-3-amino-5-(1-ethylpropoxy)c...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343682(((1S,5R,6R)-6-acetamido-3-carboxy-5-(pentan-3-ylox...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343683((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(3-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343684((3S,4R,5R)-4-Acetamido-5-(1-ethyl-propoxy)-3-[4-(1...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
TargetSialidase-3(Homo sapiens (Human))
University of Alberta

Curated by ChEMBL
LigandPNGBDBM50343685((3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(1-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human NEU3 using 4MU-NA as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZZVPubMed
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