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BDBM50184651 CHEMBL377093::{4-[4,6-bis-(4-trifluoromethyl-phenyl)-pyrimidin-2-ylmethoxy]-2-methyl-phenoxy}-acetic acid

SMILES: Cc1cc(OCc2nc(cc(n2)-c2ccc(cc2)C(F)(F)F)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O

InChI Key: InChIKey=REVAIOHTAHULEP-UHFFFAOYSA-N

Data: 3 EC50

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 = 50184651   
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))
BDBM50184651
PNG
(CHEMBL377093 | {4-[4,6-bis-(4-trifluoromethyl-phen...)
Show SMILES Cc1cc(OCc2nc(cc(n2)-c2ccc(cc2)C(F)(F)F)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O
Show InChI InChI=1S/C28H20F6N2O4/c1-16-12-21(10-11-24(16)40-15-26(37)38)39-14-25-35-22(17-2-6-19(7-3-17)27(29,30)31)13-23(36-25)18-4-8-20(9-5-18)28(32,33)34/h2-13H,14-15H2,1H3,(H,37,38)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 40n/an/an/an/a



The Genomics Institute of the Novartis Research Foundation

Curated by ChEMBL


Assay Description
Effect on human PPARdelta transactivation in 293T cells


Bioorg Med Chem Lett 16: 2969-73 (2006)


Article DOI: 10.1016/j.bmcl.2006.02.079
BindingDB Entry DOI: 10.7270/Q2XW4JDG
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha


(Homo sapiens (Human))
BDBM50184651
PNG
(CHEMBL377093 | {4-[4,6-bis-(4-trifluoromethyl-phen...)
Show SMILES Cc1cc(OCc2nc(cc(n2)-c2ccc(cc2)C(F)(F)F)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O
Show InChI InChI=1S/C28H20F6N2O4/c1-16-12-21(10-11-24(16)40-15-26(37)38)39-14-25-35-22(17-2-6-19(7-3-17)27(29,30)31)13-23(36-25)18-4-8-20(9-5-18)28(32,33)34/h2-13H,14-15H2,1H3,(H,37,38)
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
Effect on human PPARalpha transactivation in 293T cells


Bioorg Med Chem Lett 16: 2969-73 (2006)


Article DOI: 10.1016/j.bmcl.2006.02.079
BindingDB Entry DOI: 10.7270/Q2XW4JDG
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))
BDBM50184651
PNG
(CHEMBL377093 | {4-[4,6-bis-(4-trifluoromethyl-phen...)
Show SMILES Cc1cc(OCc2nc(cc(n2)-c2ccc(cc2)C(F)(F)F)-c2ccc(cc2)C(F)(F)F)ccc1OCC(O)=O
Show InChI InChI=1S/C28H20F6N2O4/c1-16-12-21(10-11-24(16)40-15-26(37)38)39-14-25-35-22(17-2-6-19(7-3-17)27(29,30)31)13-23(36-25)18-4-8-20(9-5-18)28(32,33)34/h2-13H,14-15H2,1H3,(H,37,38)
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
Effect on human PPARgamma transactivation in 293T cells


Bioorg Med Chem Lett 16: 2969-73 (2006)


Article DOI: 10.1016/j.bmcl.2006.02.079
BindingDB Entry DOI: 10.7270/Q2XW4JDG
More data for this
Ligand-Target Pair