Found 37 hits of Enzyme Inhibition Constant Data Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50344341
(CHEMBL255593 | rac-2-(3-(benzamidomethyl)-4-methox...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccccc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C20H23NO4/c1-3-15(20(23)24)11-14-9-10-18(25-2)17(12-14)13-21-19(22)16-7-5-4-6-8-16/h4-10,12,15H,3,11,13H2,1-2H3,(H,21,22)(H,23,24) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 1.70E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50231513
((+/-)-2-{3-[(4-Adamantan-1-yl-benzoylamino)-methyl...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21,18:21:24:28.27.26| Show InChI InChI=1S/C30H37NO4/c1-3-23(29(33)34)13-19-4-9-27(35-2)25(14-19)18-31-28(32)24-5-7-26(8-6-24)30-15-20-10-21(16-30)12-22(11-20)17-30/h4-9,14,20-23H,3,10-13,15-18H2,1-2H3,(H,31,32)(H,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 120 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50373706
(CHEMBL270801)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C2CCCCC2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H33NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h9-14,16,19-20H,3-8,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 300 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50344331
(CHEMBL270587 | rac-2-(3-{[(biphenyl-4-carbonyl)-am...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)-c2ccccc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H27NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h4-14,16,19H,3,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 210 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | n/a | n/a | 61 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | n/a | n/a | 70 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373705
(CHEMBL270665)Show SMILES COc1ccc(CC(C)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:7.7,TLB:21:24:27.26.31:29,THB:25:26:29:33.24.32,25:24:27.26.31:29,32:24:27:31.30.29,32:30:27:33.25.24| Show InChI InChI=1S/C29H35NO4/c1-18(28(32)33)9-19-3-8-26(34-2)24(13-19)17-30-27(31)23-4-6-25(7-5-23)29-14-20-10-21(15-29)12-22(11-20)16-29/h3-8,13,18,20-22H,9-12,14-17H2,1-2H3,(H,30,31)(H,32,33) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 280 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50344331
(CHEMBL270587 | rac-2-(3-{[(biphenyl-4-carbonyl)-am...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)-c2ccccc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H27NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h4-14,16,19H,3,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 320 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50344331
(CHEMBL270587 | rac-2-(3-{[(biphenyl-4-carbonyl)-am...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)-c2ccccc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H27NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h4-14,16,19H,3,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 6 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 120 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 220 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50344340
(CHEMBL255392 | rac-2-(3-(4-Methylbenzamidomethyl)-...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(C)cc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C21H25NO4/c1-4-16(21(24)25)11-15-7-10-19(26-3)18(12-15)13-22-20(23)17-8-5-14(2)6-9-17/h5-10,12,16H,4,11,13H2,1-3H3,(H,22,23)(H,24,25) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 9.40E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373702
(CHEMBL255426)Show SMILES CCCCCCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:12.11,TLB:27:30:33.32.37:35,THB:31:32:35:39.30.38,31:30:33.32.37:35,38:30:33:37.36.35,38:36:33:39.31.30| Show InChI InChI=1S/C35H47NO4/c1-3-5-6-7-14-40-32-13-8-24(18-28(4-2)34(38)39)19-30(32)23-36-33(37)29-9-11-31(12-10-29)35-20-25-15-26(21-35)17-27(16-25)22-35/h8-13,19,25-28H,3-7,14-18,20-23H2,1-2H3,(H,36,37)(H,38,39) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 620 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373707
(CHEMBL271877)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C(C)(C)C)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C24H31NO4/c1-6-17(23(27)28)13-16-7-12-21(29-5)19(14-16)15-25-22(26)18-8-10-20(11-9-18)24(2,3)4/h7-12,14,17H,6,13,15H2,1-5H3,(H,25,26)(H,27,28) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 37 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50373704
(CHEMBL270451)Show SMILES CCCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |w:3.3,TLB:19:22:25.24.29:27,THB:23:24:27:31.22.30,23:22:25.24.29:27,30:22:25:29.28.27,30:28:25:31.23.22| Show InChI InChI=1S/C31H39NO4/c1-3-4-25(30(34)35)14-20-5-10-28(36-2)26(15-20)19-32-29(33)24-6-8-27(9-7-24)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-23,25H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50335273
((R)-2-{3-[(4-adamantan-1-yl-benzoylamino)-methyl]-...)Show SMILES CCCOc1ccc(C[C@@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m1/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 83 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | n/a | n/a | 43 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373703
(CHEMBL270664)Show SMILES CCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:8.7,TLB:23:26:29.28.33:31,THB:27:28:31:35.26.34,27:26:29.28.33:31,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C31H39NO4/c1-3-24(30(34)35)14-20-5-10-28(36-4-2)26(15-20)19-32-29(33)25-6-8-27(9-7-25)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-24H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 50 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373707
(CHEMBL271877)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C(C)(C)C)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C24H31NO4/c1-6-17(23(27)28)13-16-7-12-21(29-5)19(14-16)15-25-22(26)18-8-10-20(11-9-18)24(2,3)4/h7-12,14,17H,6,13,15H2,1-5H3,(H,25,26)(H,27,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373706
(CHEMBL270801)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C2CCCCC2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H33NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h9-14,16,19-20H,3-8,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 4 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50344340
(CHEMBL255392 | rac-2-(3-(4-Methylbenzamidomethyl)-...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(C)cc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C21H25NO4/c1-4-16(21(24)25)11-15-7-10-19(26-3)18(12-15)13-22-20(23)17-8-5-14(2)6-9-17/h5-10,12,16H,4,11,13H2,1-3H3,(H,22,23)(H,24,25) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 100 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373704
(CHEMBL270451)Show SMILES CCCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |w:3.3,TLB:19:22:25.24.29:27,THB:23:24:27:31.22.30,23:22:25.24.29:27,30:22:25:29.28.27,30:28:25:31.23.22| Show InChI InChI=1S/C31H39NO4/c1-3-4-25(30(34)35)14-20-5-10-28(36-2)26(15-20)19-32-29(33)24-6-8-27(9-7-24)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-23,25H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 140 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50231513
((+/-)-2-{3-[(4-Adamantan-1-yl-benzoylamino)-methyl...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21,18:21:24:28.27.26| Show InChI InChI=1S/C30H37NO4/c1-3-23(29(33)34)13-19-4-9-27(35-2)25(14-19)18-31-28(32)24-5-7-26(8-6-24)30-15-20-10-21(16-30)12-22(11-20)17-30/h4-9,14,20-23H,3,10-13,15-18H2,1-2H3,(H,31,32)(H,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 95 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50335273
((R)-2-{3-[(4-adamantan-1-yl-benzoylamino)-methyl]-...)Show SMILES CCCOc1ccc(C[C@@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 870 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50373702
(CHEMBL255426)Show SMILES CCCCCCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:12.11,TLB:27:30:33.32.37:35,THB:31:32:35:39.30.38,31:30:33.32.37:35,38:30:33:37.36.35,38:36:33:39.31.30| Show InChI InChI=1S/C35H47NO4/c1-3-5-6-7-14-40-32-13-8-24(18-28(4-2)34(38)39)19-30(32)23-36-33(37)29-9-11-31(12-10-29)35-20-25-15-26(21-35)17-27(16-25)22-35/h8-13,19,25-28H,3-7,14-18,20-23H2,1-2H3,(H,36,37)(H,38,39) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 810 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373704
(CHEMBL270451)Show SMILES CCCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |w:3.3,TLB:19:22:25.24.29:27,THB:23:24:27:31.22.30,23:22:25.24.29:27,30:22:25:29.28.27,30:28:25:31.23.22| Show InChI InChI=1S/C31H39NO4/c1-3-4-25(30(34)35)14-20-5-10-28(36-2)26(15-20)19-32-29(33)24-6-8-27(9-7-24)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-23,25H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 120 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50373706
(CHEMBL270801)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C2CCCCC2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C26H33NO4/c1-3-19(26(29)30)15-18-9-14-24(31-2)23(16-18)17-27-25(28)22-12-10-21(11-13-22)20-7-5-4-6-8-20/h9-14,16,19-20H,3-8,15,17H2,1-2H3,(H,27,28)(H,29,30) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 220 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373702
(CHEMBL255426)Show SMILES CCCCCCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:12.11,TLB:27:30:33.32.37:35,THB:31:32:35:39.30.38,31:30:33.32.37:35,38:30:33:37.36.35,38:36:33:39.31.30| Show InChI InChI=1S/C35H47NO4/c1-3-5-6-7-14-40-32-13-8-24(18-28(4-2)34(38)39)19-30(32)23-36-33(37)29-9-11-31(12-10-29)35-20-25-15-26(21-35)17-27(16-25)22-35/h8-13,19,25-28H,3-7,14-18,20-23H2,1-2H3,(H,36,37)(H,38,39) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50231507
((2S)-2-(4-propoxy-3-{[({4-[(3S,5S,7S)-tricyclo[3.3...)Show SMILES CCCOc1ccc(C[C@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |r,TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27,24:27:30:34.33.32| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Similars
| PDB
Article
PubMed
| n/a | n/a | n/a | n/a | 140 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50373703
(CHEMBL270664)Show SMILES CCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:8.7,TLB:23:26:29.28.33:31,THB:27:28:31:35.26.34,27:26:29.28.33:31,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C31H39NO4/c1-3-24(30(34)35)14-20-5-10-28(36-4-2)26(15-20)19-32-29(33)25-6-8-27(9-7-25)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-24H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 250 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50373707
(CHEMBL271877)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C(C)(C)C)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C24H31NO4/c1-6-17(23(27)28)13-16-7-12-21(29-5)19(14-16)15-25-22(26)18-8-10-20(11-9-18)24(2,3)4/h7-12,14,17H,6,13,15H2,1-5H3,(H,25,26)(H,27,28) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 720 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50335273
((R)-2-{3-[(4-adamantan-1-yl-benzoylamino)-methyl]-...)Show SMILES CCCOc1ccc(C[C@@H](CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |TLB:24:27:30.29.34:32,THB:28:29:32:36.27.35,28:27:30.29.34:32,35:27:30:34.33.32,35:33:30:36.28.27| Show InChI InChI=1S/C32H41NO4/c1-3-11-37-29-10-5-21(15-25(4-2)31(35)36)16-27(29)20-33-30(34)26-6-8-28(9-7-26)32-17-22-12-23(18-32)14-24(13-22)19-32/h5-10,16,22-25H,3-4,11-15,17-20H2,1-2H3,(H,33,34)(H,35,36)/t22?,23?,24?,25-,32?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 500 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373703
(CHEMBL270664)Show SMILES CCOc1ccc(CC(CC)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:8.7,TLB:23:26:29.28.33:31,THB:27:28:31:35.26.34,27:26:29.28.33:31,34:26:29:33.32.31,34:32:29:35.27.26| Show InChI InChI=1S/C31H39NO4/c1-3-24(30(34)35)14-20-5-10-28(36-4-2)26(15-20)19-32-29(33)25-6-8-27(9-7-25)31-16-21-11-22(17-31)13-23(12-21)18-31/h5-10,15,21-24H,3-4,11-14,16-19H2,1-2H3,(H,32,33)(H,34,35) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 28 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50373705
(CHEMBL270665)Show SMILES COc1ccc(CC(C)C(O)=O)cc1CNC(=O)c1ccc(cc1)C12CC3CC(CC(C3)C1)C2 |w:7.7,TLB:21:24:27.26.31:29,THB:25:26:29:33.24.32,25:24:27.26.31:29,32:24:27:31.30.29,32:30:27:33.25.24| Show InChI InChI=1S/C29H35NO4/c1-18(28(32)33)9-19-3-8-26(34-2)24(13-19)17-30-27(31)23-4-6-25(7-5-23)29-14-20-10-21(15-29)12-22(11-20)16-29/h3-8,13,18,20-22H,9-12,14-17H2,1-2H3,(H,30,31)(H,32,33) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 41 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50231513
((+/-)-2-{3-[(4-Adamantan-1-yl-benzoylamino)-methyl...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(cc2)C23CC4CC(CC(C4)C2)C3)c1)C(O)=O |TLB:18:21:24.23.28:26,THB:22:23:26:30.21.29,22:21:24.23.28:26,29:21:24:28.27.26,29:27:24:30.22.21,18:21:24:28.27.26| Show InChI InChI=1S/C30H37NO4/c1-3-23(29(33)34)13-19-4-9-27(35-2)25(14-19)18-31-28(32)24-5-7-26(8-6-24)30-15-20-10-21(16-30)12-22(11-20)17-30/h4-9,14,20-23H,3,10-13,15-18H2,1-2H3,(H,31,32)(H,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50344340
(CHEMBL255392 | rac-2-(3-(4-Methylbenzamidomethyl)-...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccc(C)cc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C21H25NO4/c1-4-16(21(24)25)11-15-7-10-19(26-3)18(12-15)13-22-20(23)17-8-5-14(2)6-9-17/h5-10,12,16H,4,11,13H2,1-3H3,(H,22,23)(H,24,25) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 3.80E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM50344341
(CHEMBL255593 | rac-2-(3-(benzamidomethyl)-4-methox...)Show SMILES CCC(Cc1ccc(OC)c(CNC(=O)c2ccccc2)c1)C(O)=O |w:2.2| Show InChI InChI=1S/C20H23NO4/c1-3-15(20(23)24)11-14-9-10-18(25-2)17(12-14)13-21-19(22)16-7-5-4-6-8-16/h4-10,12,15H,3,11,13H2,1-2H3,(H,21,22)(H,23,24) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 8.10E+3 | n/a | n/a | n/a | n/a |
University of Tokyo
Curated by ChEMBL
| Assay Description
Agonist activity at human recombinant PPARdelta in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1110-5 (2008)
Article DOI: 10.1016/j.bmcl.2007.12.001
BindingDB Entry DOI: 10.7270/Q2FX7B9S |
More data for this
Ligand-Target Pair | |
Search and Browse
