Compile Data Set for Download or QSAR
Found 97 with Last Name = 'tai' and Initial = 'bh'
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM25737(12-[(adamantan-1-ylcarbamoyl)amino]dodecanoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50140241(Allopurinol | Aloral | Aluline 100 | Aluline 300 |...)copy SMILEScopy InChI
Affinity DataIC50: 3.89E+3nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Catholic University of Daegu

Curated by ChEMBL
LigandPNGBDBM50141095(CHEMBL3754276)copy SMILEScopy InChI
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibition of mushroom tyrosinase using L-tyrosine as substrate measured every 1 min for 20 mins by spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ05M2PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004202(CHEBI:75813 | CHEMBL1221722)copy SMILEScopy InChI
Affinity DataIC50: 1.72E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004200(CHEMBL459260)copy SMILEScopy InChI
Affinity DataIC50: 1.81E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004201(CHEMBL3236511)copy SMILEScopy InChI
Affinity DataIC50: 1.86E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM4078(6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.0...)copy SMILEScopy InChI
Affinity DataIC50: 2.07E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50241367(2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-((2S,4R,5...)copy SMILEScopy InChI
Affinity DataIC50: 2.18E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004198(CHEMBL3236510)copy SMILEScopy InChI
Affinity DataIC50: 2.38E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50217942(2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chr...)copy SMILEScopy InChI
Affinity DataIC50: 2.43E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004199(CHEMBL444191)copy SMILEScopy InChI
Affinity DataIC50: 2.74E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50241354(2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-tr...)copy SMILEScopy InChI
Affinity DataIC50: 2.84E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)copy SMILEScopy InChI
Affinity DataIC50: 3.35E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004197(CHEMBL3236509)copy SMILEScopy InChI
Affinity DataIC50: 3.61E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Catholic University of Daegu

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataIC50: 3.64E+4nMAssay Description:Inhibition of mushroom tyrosinase using L-tyrosine as substrate measured every 1 min for 20 mins by spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ05M2PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM20875(1-(2,4-dihydroxy-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihyd...)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004203(CHEMBL3236512)copy SMILEScopy InChI
Affinity DataIC50: 4.74E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50241243(3,4',5,7-Tetrahydroxyflavone-3-glucoside | 3-(beta...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50004204(CHEMBL3236513)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as substrate PHOME hydrolysis after 1 hr by fluorescence methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z1722PubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50203065(3-phenylacrylaldehyde | 3-phenylprop-2-enal | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485313(Cinnacasolide C)copy SMILEScopy InChI
Affinity DataIC50: 8.52E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50240642((E)-3-(2-Methoxy-phenyl)-propenal | 2-methoxy cinn...)copy SMILEScopy InChI
Affinity DataIC50: 8.63E+4nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM7568((2E)-3-(2-hydroxyphenyl)prop-2-enal | Cinnamaldehy...)copy SMILEScopy InChI
Affinity DataIC50: 1.01E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485315(Cinnacasolide B)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50485314(Cinnacasolide A)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310452(CHEMBL1083511 | rosavin)copy SMILEScopy InChI
Affinity DataIC50: 1.16E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310450(CHEMBL1087939 | methyl dihydromelilotoside)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310449(CHEMBL1087938 | dihydromelilotoside)copy SMILEScopy InChI
Affinity DataIC50: 1.52E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM16430((2E)-3-phenylprop-2-enoic acid | CHEMBL27246 | Cin...)copy SMILEScopy InChI
Affinity DataIC50: 1.75E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50146462((2E)-3-(2-hydroxyphenyl)-2-propenoic acid | (2E)-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.94E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50211193(3-(4-hydroxy-3-methoxyphenyl)prop-2-enal | CHEMBL2...)copy SMILEScopy InChI
Affinity DataIC50: 2.02E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447860(CHEMBL3114757)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM23416(α-CA inhibitor, 3 | (+)-Catechin | (2R,3S)-2-...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
National Institute of Medicinal Materials

Curated by ChEMBL
LigandPNGBDBM50310446((E)-3-Phenyl-prop-2-en-1-ol | 3-phenylprop-2-en-1-...)copy SMILEScopy InChI
Affinity DataIC50: 3.72E+5nMAssay Description:Inhibition of xanthine oxidase- mediated uric acid formation after 5 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VVZPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447857(Aescultitannin B)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447858(CHEBI:75630 | CHEMBL501490)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447859(CHEMBL3114756)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447856(CHEMBL3114755)copy SMILEScopy InChI
Affinity DataIC50: 5.20E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM23417(α-CA inhibitor, 4 | (-)-Epicatechin | (2R,3R)...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+5nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447862(CHEMBL3114760)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447861(CHEMBL3114759)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50148911((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447854(CHEMBL3114753 | CHEMBL3114754)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447854(CHEMBL3114753 | CHEMBL3114754)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447852(CHEMBL3114752)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetSucrase-isomaltase, intestinal(Rattus norvegicus (Rat))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50447853(CHEMBL1808110)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat intestinal sucrase using p-nitrophenyl-alpha-d-glucopyranoside as substrate incubated for 10 mins prior to substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM7CMJPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379791(METHYLEUGENOL | Methyl eugenol (1))copy SMILEScopy InChI
Affinity DataEC50:  4.00E+4nMAssay Description:Transactivation of GAL4-fused PPARgamma LBD expressed in HepG2 cells after 20 hrs by luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P55PHFPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379792(CHEMBL2011538)copy SMILEScopy InChI
Affinity DataEC50: >6.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha LBD expressed in HepG2 cells after 20 hrs by luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P55PHFPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379793(PLUVIATILOL)copy SMILEScopy InChI
Affinity DataEC50: >6.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha LBD expressed in HepG2 cells after 20 hrs by luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P55PHFPubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379794(PINORESINOL)copy SMILEScopy InChI
Affinity DataEC50: >6.00E+4nMAssay Description:Transactivation of GAL4-fused PPARalpha LBD expressed in HepG2 cells after 20 hrs by luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2P55PHFPubMed
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