Compile Data Set for Download or QSAR
Found 64 with Last Name = 'hosoe' and Initial = 's'
LigandPNGBDBM50590513(CHEMBL5170356)copy SMILES
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590497(CHEMBL5182987)copy SMILES
Affinity DataIC50: 15nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590511(CHEMBL5175794)copy SMILES
Affinity DataIC50: 24nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50603228(CHEMBL5194399)copy SMILES
Affinity DataIC50: 33nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603226(CHEMBL5189512)copy SMILES
Affinity DataIC50: 40nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590509(CHEMBL5188991)copy SMILES
Affinity DataIC50: 43nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590512(CHEMBL5173115)copy SMILES
Affinity DataIC50: 61nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590498(CHEMBL5171732)copy SMILES
Affinity DataIC50: 64nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590498(CHEMBL5171732)copy SMILES
Affinity DataIC50: 64nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590507(CHEMBL5206581)copy SMILES
Affinity DataIC50: 71nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50603229(CHEMBL5172873)copy SMILES
Affinity DataIC50: 83nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603218(CHEMBL5209124)copy SMILES
Affinity DataIC50: 87nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590504(CHEMBL5196753)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590503(CHEMBL5202364)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590502(CHEMBL5206927)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590506(CHEMBL5187558)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50603225(CHEMBL5174328)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603224(CHEMBL5192802)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590505(CHEMBL5193730)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590510(CHEMBL5172080)copy SMILES
Affinity DataIC50: 103nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590496(CHEMBL5174202)copy SMILES
Affinity DataIC50: 120nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590496(CHEMBL5174202)copy SMILES
Affinity DataIC50: 120nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603221(CHEMBL5203083)copy SMILES
Affinity DataIC50: 249nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590508(CHEMBL5188788)copy SMILES
Affinity DataIC50: 288nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50603227(CHEMBL5208550)copy SMILES
Affinity DataIC50: 315nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603222(CHEMBL5194891)copy SMILES
Affinity DataIC50: 354nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603220(CHEMBL5205017)copy SMILES
Affinity DataIC50: 404nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603219(CHEMBL5198191)copy SMILES
Affinity DataIC50: 455nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590496(CHEMBL5174202)copy SMILES
Affinity DataIC50: 838nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50603223(CHEMBL5188634)copy SMILES
Affinity DataIC50: 997nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7TXQPubMed
LigandPNGBDBM50590501(CHEMBL5180294)copy SMILES
Affinity DataIC50: 1.14E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590500(CHEMBL5180542)copy SMILES
Affinity DataIC50: 1.40E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
LigandPNGBDBM50590499(CHEMBL5169559)copy SMILES
Affinity DataIC50: 2.88E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2N4KPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503123(CHEMBL4545684)copy SMILEScopy InChI
Affinity DataEC50:  1nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503122(CHEMBL4470932)copy SMILEScopy InChI
Affinity DataEC50:  1.70nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503121(CHEMBL4544366)copy SMILEScopy InChI
Affinity DataEC50:  1.40nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503126(CHEMBL4570877)copy SMILEScopy InChI
Affinity DataEC50:  5.30nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503120(CHEMBL4461571)copy SMILEScopy InChI
Affinity DataEC50:  3nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503125(CHEMBL4454228)copy SMILEScopy InChI
Affinity DataEC50:  32nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503118(CHEMBL4515010)copy SMILEScopy InChI
Affinity DataEC50:  7nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503124(CHEMBL4559460)copy SMILEScopy InChI
Affinity DataEC50:  7.30nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503123(CHEMBL4545684)copy SMILEScopy InChI
Affinity DataEC50:  5.30nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503122(CHEMBL4470932)copy SMILEScopy InChI
Affinity DataEC50:  13nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503121(CHEMBL4544366)copy SMILEScopy InChI
Affinity DataEC50:  3.60nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503120(CHEMBL4461571)copy SMILEScopy InChI
Affinity DataEC50:  21nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503116(CHEMBL4579147)copy SMILEScopy InChI
Affinity DataEC50:  24nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503119(CHEMBL4518548)copy SMILEScopy InChI
Affinity DataEC50:  4.40nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503118(CHEMBL4515010)copy SMILEScopy InChI
Affinity DataEC50:  12nMAssay Description:Transactivation of chimeric GAL4-fused human PPARgamma transfected in HEK293EBNA cells measured at 24 hrs after drug treatment by steady-Glo lucifera...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50469400(CHEMBL4278109)copy SMILEScopy InChI
Affinity DataEC50:  3.30nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Hokkaido University

Curated by ChEMBL
LigandPNGBDBM50503117(CHEMBL4540607)copy SMILEScopy InChI
Affinity DataEC50:  19nMAssay Description:Agonist activity at PPARgamma in human MKN45 cells assessed as induction of cell aggregation incubated for 5 days by Hoechst 33342 staining based IN ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2T7PPubMed
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