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Found 44 with Last Name = 'lin' and Initial = 'cn'
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292544(3,4,6,7-tetrahydroxyxanthone | CHEMBL477740)
Affinity DataKi:  1.42E+4nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292547(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)
Affinity DataKi:  3.42E+4nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292546(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)
Affinity DataKi:  1.26E+5nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50155447(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)
Affinity DataKi:  2.50E+5nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  2.80E+3nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142192(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)
Affinity DataIC50:  5.90E+3nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM79181(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM79181(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142192(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)
Affinity DataIC50:  9.70E+3nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50077323(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)
Affinity DataIC50:  1.37E+4nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  1.77E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50263178(2',5'-Diethoxy-2-(5-methylthienyl)chalcone | CHEMB...)
Affinity DataIC50:  2.13E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142193(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)
Affinity DataIC50:  2.63E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142191(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50077323(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50366927(CHEMBL1159471)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142193(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50366927(CHEMBL1159471)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142190(2-((11bR,12R)-9-Hydroxy-5b,11b-dihydro-6H-3,7,12-t...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of lysozyme in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142191(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142190(2-((11bR,12R)-9-Hydroxy-5b,11b-dihydro-6H-3,7,12-t...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibitory effect of compound on the release of Beta-glucuronidase in rat neutrophils stimulated with fMLP/CBMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292544(3,4,6,7-tetrahydroxyxanthone | CHEMBL477740)
Affinity DataIC50:  3.54E+4nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340832(3-[3-(Piperidin-1-yl)-propoxy]xanthone | CHEMBL176...)
Affinity DataIC50:  3.78E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50244273(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)
Affinity DataIC50:  4.21E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50244273(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)
Affinity DataIC50:  4.21E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340843(3-Hydroxy-6-[3-(methylpiperazylamino)-propoxy]xant...)
Affinity DataIC50:  4.43E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340834(3-[3-(4-Methylpiperazino)-propoxy]xanthone | CHEMB...)
Affinity DataIC50:  4.73E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340841(3-[3-(Diethylamino)-propoxy]-6-hydroxyxanthone | C...)
Affinity DataIC50:  5.35E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340836(3-[3-(Diethylamino)-propoxy]xanthone | CHEMBL17612...)
Affinity DataIC50:  5.65E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340839(3-[3-(Cyclopropylamino)-propoxy]-6-hydroxyxanthone...)
Affinity DataIC50:  6.30E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340833(3-[3-(Pyrrolidin-1-yl)-propoxy]xanthone | CHEMBL17...)
Affinity DataIC50:  6.55E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340838(3-Hydroxy-6-[3-(pyrrolidin-1-yl)-propoxy]xanthone ...)
Affinity DataIC50:  6.88E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292547(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)
Affinity DataIC50:  6.92E+4nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340840(3-[3-(Cyclohexylamino)-propoxy]-6-hydroxyxanthone ...)
Affinity DataIC50:  7.29E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340837(3-Hydroxy-6-[3-(piperidin-1-yl)-propoxy]xanthone |...)
Affinity DataIC50:  8.23E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340842(3-Hydroxy-6-[3-(piperazino)-propoxy]xanthone | CHE...)
Affinity DataIC50:  9.19E+4nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340835(3-[3-(Piperazino)-propoxy]xanthone | CHEMBL1761211)
Affinity DataIC50:  1.09E+5nMAssay Description:Inhibition of xanthine oxidase activity assessed as uric acid formation pretreated for 15 mins before substrate addition measured after 5 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50263222(2'-Ethoxy-5'-methoxy-2-(5-methylthienyl)chalcone |...)
Affinity DataIC50:  1.31E+5nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292546(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)
Affinity DataIC50:  2.39E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50155447(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)
Affinity DataIC50:  5.31E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292545(2,3,6,7-Tethrahydroxyxanthone | CHEMBL12700)
Affinity DataIC50:  7.69E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed