Compile Data Set for Download or QSAR
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)copy SMILEScopy InChI
Affinity DataKi:  1.42E+4nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292547(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataKi:  3.42E+4nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292546(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)copy SMILEScopy InChI
Affinity DataKi:  1.26E+5nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50155447(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+5nMAssay Description:Inhibition of ACE by Lineweaver-Burk plotMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3K7RPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM35440(ALLOPURINOL | MLS000069453 | SMR000059083 | cid_20...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182BFPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142192(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM79181(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM79181(10-[3-(4-methyl-1-piperazinyl)propyl]-2-(trifluoro...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142192(3-(2,4-Dihydroxy-phenyl)-5,7-dihydroxy-chromen-4-o...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50077323(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50263178(2',5'-Diethoxy-2-(5-methylthienyl)chalcone | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2.13E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182BFPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142193(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142191(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50077323(7,4'-Dihydroxyflavone | 7-hydroxy-2-(4-hydroxyphen...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetLysozyme C-1(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50366927(CHEMBL1159471)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142193(2'-hydroxydaidzein | 3-(2,4-dihydroxyphenyl)-7-hyd...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50366927(CHEMBL1159471)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
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...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142191(5,7-Dihydroxy-3-(4-hydroxy-2-methoxy-phenyl)-chrom...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetBeta-glucuronidase(Rattus norvegicus)
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50142190(2-((11bR,12R)-9-Hydroxy-5b,11b-dihydro-6H-3,7,12-t...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2C829VGPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292544(3,4,6,7-tetrahydroxyxanthone | CHEMBL477740)copy SMILEScopy InChI
Affinity DataIC50: 3.54E+4nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340832(3-[3-(Piperidin-1-yl)-propoxy]xanthone | CHEMBL176...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50244273(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)copy SMILEScopy InChI
Affinity DataIC50: 4.21E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3K7RPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50244273(CHEMBL470950 | CHEMBL511791 | Hyperielliptone HB)copy SMILEScopy InChI
Affinity DataIC50: 4.21E+4nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25T3K7RPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340843(3-Hydroxy-6-[3-(methylpiperazylamino)-propoxy]xant...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340834(3-[3-(4-Methylpiperazino)-propoxy]xanthone | CHEMB...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340841(3-[3-(Diethylamino)-propoxy]-6-hydroxyxanthone | C...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340836(3-[3-(Diethylamino)-propoxy]xanthone | CHEMBL17612...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340839(3-[3-(Cyclopropylamino)-propoxy]-6-hydroxyxanthone...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340833(3-[3-(Pyrrolidin-1-yl)-propoxy]xanthone | CHEMBL17...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340838(3-Hydroxy-6-[3-(pyrrolidin-1-yl)-propoxy]xanthone ...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292547(1,3,5,6-tetrahydroxyxanthone | 1,3,5,6-tetrahydrox...)copy SMILEScopy InChI
Affinity DataIC50: 6.92E+4nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340840(3-[3-(Cyclohexylamino)-propoxy]-6-hydroxyxanthone ...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340837(3-Hydroxy-6-[3-(piperidin-1-yl)-propoxy]xanthone |...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340842(3-Hydroxy-6-[3-(piperazino)-propoxy]xanthone | CHE...)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50340835(3-[3-(Piperazino)-propoxy]xanthone | CHEMBL1761211)copy SMILEScopy InChI
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 Article
BindingDB Entry DOI: 10.7270/Q2RB74X9PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
Kaohsiung Medical University

Curated by ChEMBL
LigandPNGBDBM50263222(2'-Ethoxy-5'-methoxy-2-(5-methylthienyl)chalcone |...)copy SMILEScopy InChI
Affinity DataIC50: 1.31E+5nMAssay Description:Inhibition of xanthine oxidase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182BFPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292546(3,4,5,6-tetrahydroxyxanthone | CHEMBL477921 | US91...)copy SMILEScopy InChI
Affinity DataIC50: 2.39E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50155447(1,3,6,7-Tetrahydroxy-xanthen-9-one | 1,3,6,7-tetra...)copy SMILEScopy InChI
Affinity DataIC50: 5.31E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50292545(2,3,6,7-Tethrahydroxyxanthone | CHEMBL12700)copy SMILEScopy InChI
Affinity DataIC50: 7.69E+5nMAssay Description:Inhibition of ACEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1WXZPubMed