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SMILES: Cc1cc(OCc2nc(c(s2)-c2ccc(OC(F)(F)F)cc2)-c2cncnc2)ccc1OCC(O)=O

InChI Key: InChIKey=AZRLDFPSQPRAGI-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50312488   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50312488
PNG
(2-(4-((4-(Pyrimidin-5-yl)-5-(4-(trifluoromethoxy)p...)
Show SMILES Cc1cc(OCc2nc(c(s2)-c2ccc(OC(F)(F)F)cc2)-c2cncnc2)ccc1OCC(O)=O
Show InChI InChI=1S/C24H18F3N3O5S/c1-14-8-18(6-7-19(14)34-12-21(31)32)33-11-20-30-22(16-9-28-13-29-10-16)23(36-20)15-2-4-17(5-3-15)35-24(25,26)27/h2-10,13H,11-12H2,1H3,(H,31,32)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 59n/an/an/an/a



The Genomics Institute of the Novartis Research Foundation

Curated by ChEMBL


Assay Description
Agonist activity at human PPARdelta ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...


J Med Chem 53: 77-105 (2010)


Article DOI: 10.1021/jm9007399
BindingDB Entry DOI: 10.7270/Q28052RP
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))
BDBM50312488
PNG
(2-(4-((4-(Pyrimidin-5-yl)-5-(4-(trifluoromethoxy)p...)
Show SMILES Cc1cc(OCc2nc(c(s2)-c2ccc(OC(F)(F)F)cc2)-c2cncnc2)ccc1OCC(O)=O
Show InChI InChI=1S/C24H18F3N3O5S/c1-14-8-18(6-7-19(14)34-12-21(31)32)33-11-20-30-22(16-9-28-13-29-10-16)23(36-20)15-2-4-17(5-3-15)35-24(25,26)27/h2-10,13H,11-12H2,1H3,(H,31,32)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



The Genomics Institute of the Novartis Research Foundation

Curated by ChEMBL


Assay Description
Agonist activity at human PPARgamma ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...


J Med Chem 53: 77-105 (2010)


Article DOI: 10.1021/jm9007399
BindingDB Entry DOI: 10.7270/Q28052RP
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha


(Homo sapiens (Human))
BDBM50312488
PNG
(2-(4-((4-(Pyrimidin-5-yl)-5-(4-(trifluoromethoxy)p...)
Show SMILES Cc1cc(OCc2nc(c(s2)-c2ccc(OC(F)(F)F)cc2)-c2cncnc2)ccc1OCC(O)=O
Show InChI InChI=1S/C24H18F3N3O5S/c1-14-8-18(6-7-19(14)34-12-21(31)32)33-11-20-30-22(16-9-28-13-29-10-16)23(36-20)15-2-4-17(5-3-15)35-24(25,26)27/h2-10,13H,11-12H2,1H3,(H,31,32)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a



The Genomics Institute of the Novartis Research Foundation

Curated by ChEMBL


Assay Description
Agonist activity at human PPARalpha ligand binding domain expressed in human 293T cells cotransfected with Gal4-DBD by luciferase transactivation ass...


J Med Chem 53: 77-105 (2010)


Article DOI: 10.1021/jm9007399
BindingDB Entry DOI: 10.7270/Q28052RP
More data for this
Ligand-Target Pair