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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 508.9
BDBM50194633

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 9 hits in this display   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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PubMed
n/an/a 5n/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [3H]2-(4-{2-[3-(2,4-difluoro-phenyl)-1-heptyl-ureido]-ethyl}-phenoxy)-2-methyl-butyric acid from human PPARdelta by SPA


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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Article
PubMed
n/an/a 5n/an/an/an/an/an/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 gamma


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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Article
PubMed
n/an/a 61.0n/an/an/an/an/an/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 gamma


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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PubMed
n/an/a 61n/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [3H]2-methyl-2-(4-{3-[propyl-(5-pyridin-2-yl-thiophene-2-sulfonyl)-amino]-propyl}-phenoxy)-propionic acid from human PPARgamma by SPA


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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PubMed
n/an/a 4.39E+3n/an/an/an/an/an/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 alpha


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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Article
PubMed
n/an/a 4.39E+3n/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [3H]2-(4-{2-[3-(2,4-difluoro-phenyl)-1-heptyl-ureido]-ethyl}-phenoxy)-2-methyl-butyric acid from human PPARalpha by SPA


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
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Article
PubMed
n/an/an/an/a 2.07E+3n/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Transactivation of human PPARalpha in CV1 cells by luciferase reporter gene assay


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
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CHEMBL
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PC sid
UniChem

Patents


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Article
PubMed
n/an/an/an/a 73n/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Transactivation of human PPARdelta in CV1 cells by luciferase reporter gene assay


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))
BDBM50194633
PNG
((R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2...)
Show SMILES C[C@H](CCOc1ccc(CCC(O)=O)c(c1)C(F)(F)F)Oc1ccc(Cl)cc1Oc1ccccc1
Show InChI InChI=1S/C26H24ClF3O5/c1-17(34-23-11-9-19(27)15-24(23)35-20-5-3-2-4-6-20)13-14-33-21-10-7-18(8-12-25(31)32)22(16-21)26(28,29)30/h2-7,9-11,15-17H,8,12-14H2,1H3,(H,31,32)/t17-/m1/s1
PDB
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Article
PubMed
n/an/an/an/a 355n/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Transactivation of human PPARgamma in CV1 cells by luciferase reporter gene assay


J Med Chem 49: 5649-52 (2006)


Article DOI: 10.1021/jm060617c
BindingDB Entry DOI: 10.7270/Q2K073WF
More data for this
Ligand-Target Pair