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BDBM50418134 CHEMBL1760273

SMILES: CCCCN(c1cccc(c1C)-c1ccc(Cl)cc1)S(=O)(=O)c1ccc(O[C@H](C)C(O)=O)c(C)c1C

InChI Key: InChIKey=FMXAKYUKNGWYKW-OAQYLSRUSA-N

Data: 3 IC50  1 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 4 hits for monomerid = 50418134   
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


(Homo sapiens (Human))
BDBM50418134
PNG
(CHEMBL1760273)
Show SMILES CCCCN(c1cccc(c1C)-c1ccc(Cl)cc1)S(=O)(=O)c1ccc(O[C@H](C)C(O)=O)c(C)c1C |r|
Show InChI InChI=1S/C28H32ClNO5S/c1-6-7-17-30(25-10-8-9-24(20(25)4)22-11-13-23(29)14-12-22)36(33,34)27-16-15-26(18(2)19(27)3)35-21(5)28(31)32/h8-16,21H,6-7,17H2,1-5H3,(H,31,32)/t21-/m1/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/an/a 6.31E+3n/an/an/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Displacement of [3H]GW 2433 from human PPARgamma by scintillation proximity assay


Bioorg Med Chem Lett 21: 2345-50 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.077
BindingDB Entry DOI: 10.7270/Q2M61MHT
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50418134
PNG
(CHEMBL1760273)
Show SMILES CCCCN(c1cccc(c1C)-c1ccc(Cl)cc1)S(=O)(=O)c1ccc(O[C@H](C)C(O)=O)c(C)c1C |r|
Show InChI InChI=1S/C28H32ClNO5S/c1-6-7-17-30(25-10-8-9-24(20(25)4)22-11-13-23(29)14-12-22)36(33,34)27-16-15-26(18(2)19(27)3)35-21(5)28(31)32/h8-16,21H,6-7,17H2,1-5H3,(H,31,32)/t21-/m1/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 13n/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Partial agonist activity at human PPARdelta expressed in african green monkey CV1 cells transfected with Gal4 assessed as beta-galactosidase activity...


Bioorg Med Chem Lett 21: 2345-50 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.077
BindingDB Entry DOI: 10.7270/Q2M61MHT
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor delta


(Homo sapiens (Human))
BDBM50418134
PNG
(CHEMBL1760273)
Show SMILES CCCCN(c1cccc(c1C)-c1ccc(Cl)cc1)S(=O)(=O)c1ccc(O[C@H](C)C(O)=O)c(C)c1C |r|
Show InChI InChI=1S/C28H32ClNO5S/c1-6-7-17-30(25-10-8-9-24(20(25)4)22-11-13-23(29)14-12-22)36(33,34)27-16-15-26(18(2)19(27)3)35-21(5)28(31)32/h8-16,21H,6-7,17H2,1-5H3,(H,31,32)/t21-/m1/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 25n/an/an/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Displacement of [3H]GW 2433 from human PPARdelta by scintillation proximity assay


Bioorg Med Chem Lett 21: 2345-50 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.077
BindingDB Entry DOI: 10.7270/Q2M61MHT
More data for this
Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (PPAR alpha)


(Homo sapiens (Human))
BDBM50418134
PNG
(CHEMBL1760273)
Show SMILES CCCCN(c1cccc(c1C)-c1ccc(Cl)cc1)S(=O)(=O)c1ccc(O[C@H](C)C(O)=O)c(C)c1C |r|
Show InChI InChI=1S/C28H32ClNO5S/c1-6-7-17-30(25-10-8-9-24(20(25)4)22-11-13-23(29)14-12-22)36(33,34)27-16-15-26(18(2)19(27)3)35-21(5)28(31)32/h8-16,21H,6-7,17H2,1-5H3,(H,31,32)/t21-/m1/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.00E+4n/an/an/an/an/an/a



GlaxoSmithKline Pharmaceuticals

Curated by ChEMBL


Assay Description
Displacement of [3H]GW 2433 from human PPARalpha by scintillation proximity assay


Bioorg Med Chem Lett 21: 2345-50 (2011)


Article DOI: 10.1016/j.bmcl.2011.02.077
BindingDB Entry DOI: 10.7270/Q2M61MHT
More data for this
Ligand-Target Pair