Found 7 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 gamma
(Homo sapiens (Human)) | BDBM50500150
(CHEMBL3746821)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3ccc(cc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-9-21(10-6-18)28-26(32)23-16-22(11-12-25(23)30-13-3-2-4-14-30)31-17-20-8-7-19(27(33)34)15-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Agonist activity at PPARgamma (unknown origin) |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Retinoic acid receptor RXR-alpha
(Homo sapiens (Human)) | BDBM50500150
(CHEMBL3746821)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3ccc(cc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-9-21(10-6-18)28-26(32)23-16-22(11-12-25(23)30-13-3-2-4-14-30)31-17-20-8-7-19(27(33)34)15-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Agonist activity at RXRalpha (unknown origin) |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Peroxisome proliferator-activated receptor alpha
(Homo sapiens (Human)) | BDBM50500150
(CHEMBL3746821)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3ccc(cc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-9-21(10-6-18)28-26(32)23-16-22(11-12-25(23)30-13-3-2-4-14-30)31-17-20-8-7-19(27(33)34)15-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Agonist activity at PPARalpha (unknown origin) |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Bile acid receptor
(Homo sapiens (Human)) | BDBM50500150
(CHEMBL3746821)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3ccc(cc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-9-21(10-6-18)28-26(32)23-16-22(11-12-25(23)30-13-3-2-4-14-30)31-17-20-8-7-19(27(33)34)15-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Agonist activity at FXR (unknown origin) |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Lipoprotein lipase
(Bos taurus) | BDBM50500148
(CHEMBL3746381)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)N2C(=O)c3ccc(cc3C2=O)C(O)=O)cc1 Show InChI InChI=1S/C28H25N3O5/c1-17-5-8-19(9-6-17)29-25(32)23-16-20(10-12-24(23)30-13-3-2-4-14-30)31-26(33)21-11-7-18(28(35)36)15-22(21)27(31)34/h5-12,15-16H,2-4,13-14H2,1H3,(H,29,32)(H,35,36) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| Purchase
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | 6.60E+3 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Induction of bovine LPL stabilization using intralipid as substrate preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate add... |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Lipoprotein lipase
(Bos taurus) | BDBM50500149
(CHEMBL3747367)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3cc(ccc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-8-21(9-6-18)28-26(32)23-16-22(10-12-25(23)30-13-3-2-4-14-30)31-17-20-15-19(27(33)34)7-11-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Induction of bovine LPL stabilization using intralipid as substrate preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate add... |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
Lipoprotein lipase
(Bos taurus) | BDBM50500150
(CHEMBL3746821)Show SMILES Cc1ccc(NC(=O)c2cc(ccc2N2CCCCC2)-n2cc3ccc(cc3n2)C(O)=O)cc1 Show InChI InChI=1S/C27H26N4O3/c1-18-5-9-21(10-6-18)28-26(32)23-16-22(11-12-25(23)30-13-3-2-4-14-30)31-17-20-8-7-19(27(33)34)15-24(20)29-31/h5-12,15-17H,2-4,13-14H2,1H3,(H,28,32)(H,33,34) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | n/a | n/a | 6.00E+3 | n/a | n/a | n/a | n/a |
Ume£ University
Curated by ChEMBL
| Assay Description
Induction of bovine LPL stabilization using intralipid as substrate preincubated for 10 mins with human recombinant ANGPTL4 followed by substrate add... |
Eur J Med Chem 103: 191-209 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.058
BindingDB Entry DOI: 10.7270/Q2W95D6B |
More data for this
Ligand-Target Pair | |
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