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Found 58 with Last Name = 'han' and Initial = 'yr'
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093525(taiwaniaflavone)
Affinity DataKi:  4.50E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50259862(13,II8-biapigenin | 3,8''-biapigenin | CHEMBL51525...)
Affinity DataKi:  4.60E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50148911((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...)
Affinity DataKi:  6.40E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50323212(6-[5-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydro...)
Affinity DataKi:  6.80E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50129952(2-(3-(5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-c...)
Affinity DataKi:  7.80E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093524(CHEMBL3585680)
Affinity DataKi:  1.04E+4nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50323213(CHEMBL1208973 | cupressuflavone)
Affinity DataKi:  1.07E+4nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093523(CHEMBL3585679 | PTP1B spring 6 (6))
Affinity DataKi:  1.45E+4nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329696((3-Bromo-4,5-dihydroxyphenyl)(2,3-dibromo-4,5-dihy...)
Affinity DataIC50:  2.65E+3nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50148911((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...)
Affinity DataIC50:  3.40E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093526(CHEMBL426373 | RK-682)
Affinity DataIC50:  4.50E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50259862(13,II8-biapigenin | 3,8''-biapigenin | CHEMBL51525...)
Affinity DataIC50:  4.50E+3nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093525(taiwaniaflavone)
Affinity DataIC50:  5.40E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50323212(6-[5-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydro...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50129952(2-(3-(5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-c...)
Affinity DataIC50:  7.40E+3nMAssay Description:Inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 mins by micr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329695(Bis(3-bromo-4,5-dihydroxyphenyl)methanone | CHEMBL...)
Affinity DataIC50:  8.89E+3nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50323213(CHEMBL1208973 | cupressuflavone)
Affinity DataIC50:  9.60E+3nMAssay Description:Competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 20 ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093524(CHEMBL3585680)
Affinity DataIC50:  9.80E+3nMAssay Description:Uncompetitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured after 2...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329693(Bis(2,3-dibromo-4,5-dihydroxyphenyl)ether | CHEMBL...)
Affinity DataIC50:  1.16E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Catholic University Of Daegu

Curated by ChEMBL
LigandPNGBDBM50093523(CHEMBL3585679 | PTP1B spring 6 (6))
Affinity DataIC50:  1.32E+4nMAssay Description:Mixed-competitive inhibition of human recombinant PTP1B using p-NPP as substrate preincubated for 10 mins followed by substrate addition measured aft...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329699(2,2',3-Tribromo-4,4',5,5'-tetrahydroxybibenzyl | C...)
Affinity DataIC50:  1.48E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329700((2-Bromo-4,5-dihydroxybenzyl)(2,3-dibromo-4,5-dihy...)
Affinity DataIC50:  1.56E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329688(2,2',3,3'-tetrabromo-4,4',5,5'-tetrahydroxydipheny...)
Affinity DataIC50:  1.84E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329698(2,2'-Dibromo-4,4',5,5'-tetrahydroxybibenzyl | CHEM...)
Affinity DataIC50:  2.12E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329694(Bis(3,4-dihydroxyphenyl)methanone | CHEMBL1269420 ...)
Affinity DataIC50:  2.26E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331609(6-methoxy-1-phenyl-4,9-dihydro-3H-pyrido[3,4-b]ind...)
Affinity DataIC50:  2.50E+4nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329701(CHEMBL491516 | bis(2, 3-dibromo-4,5-dihydroxybenzy...)
Affinity DataIC50:  2.81E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329692(Bis(2-bromo-4,5-dihydroxyphenyl)ether | CHEMBL1269...)
Affinity DataIC50:  3.09E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329689(2,2'-dibromo-4,4',5,5'-tetrahydroxydiphenylmethane...)
Affinity DataIC50:  4.62E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50274515(3-nitropropanoic acid | 3-nitropropionic acid | Bo...)
Affinity DataIC50:  5.07E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50274515(3-nitropropanoic acid | 3-nitropropionic acid | Bo...)
Affinity DataIC50:  5.07E+4nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50274515(3-nitropropanoic acid | 3-nitropropionic acid | Bo...)
Affinity DataIC50:  5.10E+4nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329697(4,4'-(ethane-1,2-diyl)dibenzene-1,2-diol | CHEMBL1...)
Affinity DataIC50:  5.85E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331604(2-(2-methyl-1H-indol-3-yl)-2-oxo-N-phenylacetamide...)
Affinity DataIC50:  6.10E+4nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329691((2-Bromo-4,5-dihydroxyphenyl)(3,4-dihydroxyphenyl)...)
Affinity DataIC50:  6.82E+4nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50102183((1H-Indol-3-yl)-oxo-acetic acid | CHEMBL57285 | in...)
Affinity DataIC50:  6.90E+4nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50206193(1-(3-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3...)
Affinity DataIC50:  7.50E+4nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50276442(CHEMBL459354 | hyrtiosin B)
Affinity DataIC50:  8.90E+4nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50276442(CHEMBL459354 | hyrtiosin B)
Affinity DataIC50:  8.90E+4nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331608(1-phenyl-4,9-dihydro-3H-pyrido[3,4-b]indole | CHEM...)
Affinity DataIC50:  9.70E+4nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50329690(4,4'-oxydibenzene-1,2-diol | CHEMBL1269392)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Candida albicans ATCC 10231 isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331606(1-phenyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-...)
Affinity DataIC50:  1.06E+5nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331607(6-methoxy-1-phenyl-2,3,4,9-tetrahydro-1H-pyrido[3,...)
Affinity DataIC50:  1.15E+5nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331605(2-(2-methyl-1H-indol-3-yl)-2-oxoacetic acid | CHEM...)
Affinity DataIC50:  1.33E+5nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50331610(1-(naphthalen-2-yl)-2,3,4,9-tetrahydro-1H-pyrido[3...)
Affinity DataIC50:  1.37E+5nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50331603(2-(1H-Indol-3-yl)-2-oxo-N-phenyl-acetamide | 2-(1H...)
Affinity DataIC50:  1.74E+5nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50331611(1-(4-methoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3...)
Affinity DataIC50:  1.80E+5nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50276441(5-hydroxyindole-3-carbaldehyde | CHEMBL506465)
Affinity DataIC50:  2.47E+5nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIsocitrate lyase(Candida albicans)
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50276441(5-hydroxyindole-3-carbaldehyde | CHEMBL506465)
Affinity DataIC50:  2.47E+5nMAssay Description:Inhibition of Candida albicans isocitrate lyaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSortase family protein(Staphylococcus aureus)
Institute

Curated by ChEMBL
LigandPNGBDBM50276408(1-carboxy-6-hydroxy-3,4-dihydro-beta-carboline | C...)
Affinity DataIC50:  2.90E+5nMAssay Description:Inhibition of Staphylococcus aureus Sortase AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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