Compile Data Set for Download or QSAR
Found 80 with Last Name = 'minh' and Initial = 'cv'
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558211(CHEMBL2332114)copy SMILES
Affinity DataKi:  1.82E+4nMAssay Description:Non competitive inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558212(3-O-Galloylquercetin | CHEMBL1935379)copy SMILES
Affinity DataKi:  2.15E+4nMAssay Description:Non competitive inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558210(CHEMBL4798780)copy SMILES
Affinity DataKi:  2.46E+4nMAssay Description:Competitive inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50379283(CHEMBL234316)copy SMILEScopy InChI
Affinity DataKi:  2.97E+4nMAssay Description:Mixed type inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558209(CHEMBL4761282)copy SMILES
Affinity DataKi:  3.71E+4nMAssay Description:Mixed type inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50056315(CHEBI:17558 | Quercitrin)copy SMILEScopy InChI
Affinity DataKi:  3.96E+4nMAssay Description:Non competitive inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558213(CHEMBL4747916)copy SMILES
Affinity DataKi:  4.55E+4nMAssay Description:Mixed type inhibition of sEH (unknown origin) using varying levels of PHOME as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50196661(12-(3-adamantan-1-yl-ureido)-dodecanoic acid butyl...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558213(CHEMBL4747916)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558212(3-O-Galloylquercetin | CHEMBL1935379)copy SMILES
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50056315(CHEBI:17558 | Quercitrin)copy SMILEScopy InChI
Affinity DataIC50: 1.18E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558211(CHEMBL2332114)copy SMILES
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558209(CHEMBL4761282)copy SMILES
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50558210(CHEMBL4798780)copy SMILES
Affinity DataIC50: 1.98E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
TargetBifunctional epoxide hydrolase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50379283(CHEMBL234316)copy SMILEScopy InChI
Affinity DataIC50: 3.01E+4nMAssay Description:Inhibition of sEH (unknown origin) assessed as reduction in 6-methoxy-2-naphthaldehyde formation using PHOME as substrate measured after 40 mins by f...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2833WP0PubMed
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
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
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
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
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
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
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
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
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
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379795(CHEMBL2011541)copy SMILEScopy InChI
Affinity DataEC50:  1.95E+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
LigandPNGBDBM50379791(METHYLEUGENOL | Methyl eugenol (1))copy SMILEScopy InChI
Affinity DataEC50:  4.65E+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
LigandPNGBDBM50379796(CHEMBL2011543)copy SMILEScopy InChI
Affinity DataEC50:  1.57E+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
LigandPNGBDBM50379797(CHEMBL2011544)copy SMILEScopy InChI
Affinity DataEC50:  4.00E+3nMAssay 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
LigandPNGBDBM50371235(CIPROFIBRATE)copy SMILEScopy InChI
Affinity DataEC50:  900nMAssay Description:Transactivation of GAL4-fused PPARalpha LBD expressed in HepG2 cells after 20 hrs by luminescence assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379792(CHEMBL2011538)copy SMILEScopy InChI
Affinity DataEC50:  2.26E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379793(PLUVIATILOL)copy SMILEScopy InChI
Affinity DataEC50:  4.87E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379794(PINORESINOL)copy SMILEScopy InChI
Affinity DataEC50:  5.86E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379798(PIPERITOL)copy SMILEScopy InChI
Affinity DataEC50:  1.89E+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
LigandPNGBDBM50379798(PIPERITOL)copy SMILEScopy InChI
Affinity DataEC50:  5.32E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379795(CHEMBL2011541)copy SMILEScopy InChI
Affinity DataEC50:  2.17E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379796(CHEMBL2011543)copy SMILEScopy InChI
Affinity DataEC50:  1.93E+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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379797(CHEMBL2011544)copy SMILEScopy InChI
Affinity DataEC50:  3.60E+3nMAssay 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 gamma(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50085045(5-((4-((6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-...)copy SMILEScopy InChI
Affinity DataEC50:  730nMAssay 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 delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379792(CHEMBL2011538)copy SMILEScopy InChI
Affinity DataEC50:  4.76E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta 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 delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379793(PLUVIATILOL)copy SMILEScopy InChI
Affinity DataEC50:  5.31E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta 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 delta(Homo sapiens (Human))
Chungnam National University

Curated by ChEMBL
LigandPNGBDBM50379794(PINORESINOL)copy SMILEScopy InChI
Affinity DataEC50:  4.95E+4nMAssay Description:Transactivation of GAL4-fused PPARbeta 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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