Found 8 hits for monomerid = 50372111 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 gamma
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/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 | 60 | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Agonist activity at PPARgamma in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 in presence of 7-benzyloxy-4-trifluoromethyl coumarin substrate |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C19
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of CYP2C19 |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | n/a | n/a | 5 | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Agonist activity at PPARalpha in HEK293 cells by GAL4 transactivation assay |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 480 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of PPARalpha |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Peroxisome proliferator-activated receptor gamma
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/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 | 670 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of PPARgamma |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of CYP2C9 |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50372111
(CHEMBL272336)Show SMILES Cc1oc(nc1CCOc1cccc(C[C@H]2[C@H](N(C2=O)c2ccc(cc2)C(C)(C)C)C(O)=O)c1)-c1ccc(Cl)cc1 Show InChI InChI=1S/C33H33ClN2O5/c1-20-28(35-30(41-20)22-8-12-24(34)13-9-22)16-17-40-26-7-5-6-21(18-26)19-27-29(32(38)39)36(31(27)37)25-14-10-23(11-15-25)33(2,3)4/h5-15,18,27,29H,16-17,19H2,1-4H3,(H,38,39)/t27-,29-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Bristol-Myers Squibb Research and Development
Curated by ChEMBL
| Assay Description Inhibition of human ERG by FLIPR assay |
Bioorg Med Chem Lett 18: 1939-44 (2008)
Article DOI: 10.1016/j.bmcl.2008.01.126 BindingDB Entry DOI: 10.7270/Q28S4QR3 |
More data for this Ligand-Target Pair | |