Found 6 hits for monomerid = 28688 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 10 | n/a | 50 | n/a | n/a | n/a | n/a |
GSK
| Assay Description Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga... |
Bioorg Med Chem Lett 18: 5018-22 (2008)
Article DOI: 10.1016/j.bmcl.2008.08.011 BindingDB Entry DOI: 10.7270/Q2WD3XWS |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha (PPAR alpha)
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.51E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
GSK
| Assay Description Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga... |
Bioorg Med Chem Lett 18: 5018-22 (2008)
Article DOI: 10.1016/j.bmcl.2008.08.011 BindingDB Entry DOI: 10.7270/Q2WD3XWS |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.51E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad Nacional Aut£noma de M£xico
Curated by ChEMBL
| Assay Description Agonist activity at PPARgamma |
Bioorg Med Chem 20: 3523-32 (2012)
Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha (PPAR alpha)
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.51E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad Nacional Aut£noma de M£xico
Curated by ChEMBL
| Assay Description Agonist activity at PPARalpha |
Bioorg Med Chem 20: 3523-32 (2012)
Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor delta
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Universidad Nacional Aut£noma de M£xico
Curated by ChEMBL
| Assay Description Agonist activity at PPARdelta |
Bioorg Med Chem 20: 3523-32 (2012)
Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor
(Homo sapiens (Human)) | BDBM28688
(5-methyl-2-({3-[(6-methyl-1H-indole-1-)sulfonyl]be...)Show SMILES Cc1ccc(NC(=O)c2cccc(c2)S(=O)(=O)n2ccc3ccc(C)cc23)c(c1)C(O)=O Show InChI InChI=1S/C24H20N2O5S/c1-15-7-9-21(20(12-15)24(28)29)25-23(27)18-4-3-5-19(14-18)32(30,31)26-11-10-17-8-6-16(2)13-22(17)26/h3-14H,1-2H3,(H,25,27)(H,28,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.51E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
GSK
| Assay Description Competition-binding curves for test compounds were determined with expressed human PPAR LBD. Plots of inhibitor concentration versus cpm of radioliga... |
Bioorg Med Chem Lett 18: 5018-22 (2008)
Article DOI: 10.1016/j.bmcl.2008.08.011 BindingDB Entry DOI: 10.7270/Q2WD3XWS |
More data for this Ligand-Target Pair | |